Lediga jobb Cytiva Sweden AB i Uppsala

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Process Safety Lead

Nytt
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn idea... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
As Process Safety Lead, your primary responsibility is to lead the systematic process safety work within Chemical Production Uppsala (CPU). You will be part of the Manufacturing Engineering leadership team and collaborate closely with cross-functional teams to ensure continuous improvements within process safety.
This position reports to the Director of Manufacturing Engineering and is based on-site at our Uppsala site.
What you will do:
Systematically lead the work to improve process safety and the safety culture within production
Initiate and drive activities to improve process safety
Lead critical incident investigations to identify contributing factors, as well as identify corrective and preventive actions
Support managers and train employees in process safety (e.g. HOP, PHA)
Be part of the department’s management team and contribute to the department’s strategic work



This role will work closely with process safety experts within our EHS department.
Who you are:
Bachelor's degree in a Science or Engineering discipline, preferably with a focus in chemistry/chemical engineering
5+ years of experience within process industry
Experience of project work/leading projects
Experience of root cause investigations and barrier analysis
Excellent communication skills (written and oral), fluent in both Swedish & English



It would be beneficial if you have previous experience with:
Lean and Continuous Improvements Visa mindre

Senior Manager - Mechanics and Fluidics

Ansök    Feb 13    Cytiva Sweden AB    Utvecklingschef
Nytt
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
The Downstream Hardware R&D organization continues to grow, we are now looking for our next Senior Manager to lead one of the Mechanical engineering development teams.
As Senior Manager for the Mechanics and Fluidics section, you will lead a team of talented engineers, be part of the department’s management team and contribute to the department’s overall mission in product development, innovation, and product care for product families like lab ÄKTA systems and Bioprocess equipment. You will play a key role in driving changes to improve ways of working and efficiency in the mechanical development work.
What you’ll do
Lead and manage a team of Mechanical engineers to ensure successful delivery of hardware designs and projects.
Drive the strategic direction of the Mechanical and Fluidics section and collaborate with other functional areas to ensure alignment with business objectives.
Monitor project timelines and budgets and make recommendations for process improvements and resource allocation.
Foster a culture of innovation and continuous improvement within the hardware engineering team.
Recruit, support and develop team members through mentorship and development opportunities.

Who you are:
MSc or similar education in the mechanical engineering field.
Experience in hardware product development, including design, development, and project management.
Proven leadership and people management skills with experience from line management or project management.
Excellent communication and collaboration skills, with the ability to work effectively with cross-functional teams.
Genuine interest in developing both people, ways of working and technical solutions.
Solution oriented, flexible, and driven, with a strong collaborative attitude.
Fluent in Swedish and English, both verbally and in writing.

Interview and selection will happen continuously, and the opening can be filled before last day of application, March 9th. For questions regarding the role please contact hiring manager Thomas Arctaedius ([email protected]). We look forward to hearing from you!
Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Process Development Project Manager

Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The Process Development Project Manager for Cytiva is responsible for interacting with the customer, from the proposal stage throughout the project, including interim and final reporting.
This position is part of the PDVS PMO located in Harborgate Portsmouth UK or Uppsala Sweden and will be onsite.
At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
What you will do:
Coordinate all phases of the project including developing proposals with input from the technical team, collaborating with commercial and legal team to ensure necessary documents are in place.
Responsible for all aspects of assigned projects including project chartering, project plan development, establishment of roles and responsibilities, resource and risk management, problem solving, team and organizational communication.
Define project planning using Visual Project Management and daily management. Establish and practice project controls/governance/standards.
Meet budgetary objectives and making adjustments to project constraints based on financial analysis. Conduct monthly invoicing for completed work, including percentage of work completed and hours booked.
Provide cost reporting information to key stakeholders.



Who you are:
Bachelor’s Degree in a science field - or equivalent (Master’s Degree preferred)
A proven background in project management.
Pharmaceutical and or GMP experience



It would be a plus if you also possess previous experience in:
Use of SmartSheets and Sales force (SFDC) Visa mindre

Field Application Scientist - EMEA

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas ... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
The "Field Application Scientist - EMEA" position for Cytiva provides technical expertise to sales representatives, resellers and customers during the sales process and works directly with customers.
This position reports to the Manager of Field Application Scientists and is part of the Genomic Medicine division in Europe and will be fully remote. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
In this role, you will have the opportunity to
Pre-sales: Play an active role within the commercial team, to promote Cytiva Nano Medicine line of products, manage leads and prospects, develop opportunities, contribute to team spirit, and improve account penetration. Attend and provide high level technical expertise at trade shows and conferences. This role should be able to evaluate a customer's process to identify solutions and provide the?necessary tools, information and support to obtain additional sales and identify new opportunities.
Develop and maintain positive relationships with customers, especially focusing on a network of key decision makers. As a team, set quarterly priorities in your territory to achieve defined business goals.?Contribute to key account plans managed by the Account Management team.
Develop a strong working knowledge of Cytiva Nano Medicine products and services, a detailed understanding of applications utilized by our customer base, as well as a strong working knowledge of the features and benefits of competitive products. Sustained evaluation or awareness of competitor activities and innovations within the marketplace generally. Develop a working knowledge of funding, market dynamics & end-user needs. Provide/facilitate efficient communication on strategic and competitive customer feedback to Marketing and Product Development teams.
Coordinate and conduct on?site and in?house customer training courses. Provide technical sales support by conducting applications?based seminars and product demonstrations. Provide applications / technical training to the sales team.
Provide phone, email, and in?person customer applications support, including troubleshooting issues related to user's technical skills, application, and instruments. Interpret customer needs and identify if the responsibility for a problem resolution falls to sales personnel, engineering, or other company personnel.

The essential requirements of the job include:
Master's Degree in biotechnologies, genomic medicines, nanomedicines OR equivalent field experience.
3+ years of applications or lab experience in a nanoparticle formulation, drug delivery, or cell biology required. Skilled in troubleshooting instrumentation, and applications.
Demonstrated superior problem solving and interpersonal and account management skills in a commercial environment. Demonstrated aptitude towards the selling process and a proven team player. Understanding of customers’ key business drivers. Ability to work independently and a self-starter with a drive for customer satisfaction.
Strong communication skills and experience delivering scientific presentations. Demonstrated technical writing ability.

Travel, Motor Vehicle Record & Physical/Environment Requirements ?:
Must be able to travel 50% in Europe

Preferred:
PhD preferred. Visa mindre

Senior Manager - Embedded Software

Ansök    Feb 13    Cytiva Sweden AB    Utvecklingschef
Nytt
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
The Downstream Hardware R&D organization continues to grow, we are now looking for a Senior Manager to lead our Embedded Software team.
As Senior Manager for the Embedded Software section, you will lead a team of talented engineers, be part of the department’s management team and contribute to the department’s overall mission in product development, innovation, and product care for product families like lab ÄKTA systems and Bioprocess equipment. You will collaborate closely with our Electronics engineering section consisting of engineers within electronics, optics and cyber security. You will play a key role in driving changes to improve ways of working and efficiency in the embedded software development work.
What you’ll do
Lead and manage a team of Embedded Software engineers to ensure successful delivery of hardware designs and projects.
Drive the strategic direction of the Embedded Software section and collaborate with other functional areas to ensure alignment with business objectives.
Monitor project timelines and budgets and make recommendations for process improvements and resource allocation.
Work for continuous improvement of the Section’s and Department’s efficiency, processes and overall ability to fulfill its tasks.
Foster a culture of innovation within the hardware engineering team.
Recruit, support and develop team members through mentorship and professional development opportunities.

Who you are:
MSc or equivalent education in a relevant discipline area.
Proven leadership and people management skills with experience from line management or project management.
Experience in hardware product development, including design, development, and project management.
Hands-on experience from software development of embedded systems.
Excellent communication and collaboration skills, with the ability to work effectively with cross-functional teams.
Genuine interest in developing both people, ways of working and technical solutions.
Solution oriented, flexible, and driven, with a strong collaborative attitude.
Fluent in Swedish and English, both verbally and in writing.

Interview and selection will happen continuously, and the opening can be filled before last day of application, March 9th. For questions regarding the role please contact hiring manager Thomas Arctaedius ([email protected]). We look forward to hearing from you!
Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Service Project Manager

Ansök    Feb 6    Cytiva Sweden AB    Utvecklingschef
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
The Service Project Manager is responsible for planning and coordinating our organization’s activities within PLP (Product Lifecycle Process) development projects, in collaboration with the primary project leaders, our service engineering leads, and the extended service teams. This role will significantly impact improvement initiatives within the global service readiness engineering organization. The Service PMO is also responsible for overseeing, developing, and maintaining the high-level service processes related to PLP.
This position report to the Sr Manager Service PMO and is part of the Global Service Readiness Engineering Team located in Uppsala, Sweden and will be an on-site role.
What you will do:
Coordinate execution of PLP (including New Product Development, Product Sustainment, and Discontinuation projects) activities and deliverables for Service
Provide input to the strategic project view for the service readiness engineering team
Interact with main project leaders for service planning, execution, status updates and deliverables
Providing high quality service deliverables within the scope of PLP projects and Global Service Readiness Engineering internal activities/projects
Supporting technical solutions and program leadership to improve the product, process or technology
Updating, improving and maintaining the high level service process related to the Cytiva PLP process



Who you are:
University Degree in Engineering or Project Management: e.g. Biomedical, Mechatronics, Systems-Engineering, or comparable qualification through work-experience
5 years relevant work experience with working in project teams meeting deadlines and deliverables – especially with global service related project activities
Effective communication skills and boundless behavior—ability to present ideas clearly and concisely
Fluent speaking and writing in English and Swedish language
Experience of defining requirement specifications (e.g. Design for Service)



It would be a plus if you also possess previous experience in:
Customer oriented attitude with effective communication skills
Self-motivated, self-starter with the ability to work independently and learn quickly
Experience with New Product Development- & Life-Cycle Management Projects



Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. Visa mindre

Processingenjör - Reningsverk & Miljö

Beskrivning av jobb Bli en del av något helt livsavgörande Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier. På Cytiva kommer du att ständigt kunna utveckla dig själv och ... Visa mer
Beskrivning av jobb
Bli en del av något helt livsavgörande
Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier.
På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbeta med utmaningar som verkligen spelar roll tillsammans med människor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i 40 länder är Cytiva en plats där varje dag är en möjlighet att lära så att du kan få fart på din karriär och förbättra dina färdigheter på lång sikt.
Vi på Cytiva är stolta över att arbeta tillsammans med en grupp av nio andra Danaher Life Sciencesföretag. Tillsammans är vi pionjärer inom vetenskap och medicin och utvecklar produkter som hjälper forskare i kampen att rädda liv.
Vi söker en processingenjör till Cytivas interna reningsverk på vår site i Uppsala. Sektionen Reningsverk & Miljö ingår i Site Business Support (SBS) och ansvarar för sitens luftemissioner, fabriksavloppsvatten och servar därmed hela vår produktionsverksamhet i Uppsala. Sektionen ansvarar för drift och tillgänglighet för reningsanläggningar, utföra mätningar av luft- och vattenemissioner och säkerställer efterlevnad på våra krav på utsläpp.
Vad du ska göra
Arbetet består av att arbeta aktivt med emissioner till luft och vatten från fabriksavloppet som kommer från våra fabriker. I rollen som processingenjör hos oss kommer du arbeta med att supporta den dagliga driften av reningsverket genom provtagning och analys, vara delaktig vid felsökning samt utveckling av reningsanläggningen. Du kommer även att, tillsammans med övrig produktionspersonal, verka för minskade emissioner, trendning av data samt delta i projekt rörande kapacitetsökningar.
Stödja operativ personal med drift, felsökning och metodförbättringar.
Utredning, utveckling och optimering av reningsprocesser för luft och vatten.
Trendning och analys av data rörande emissioner till luft och vatten från produktionen.
Utbilda personal inom produktionen för att öka medvetenheten runt emissioner.
Arbeta med reducerande åtgärder av emissioner till luft och vatten samt följa upp effektiviteten av åtgärder.
Driva change control ärenden, MOC (Management of Change) och riskanalyser inom reningsverkets ramar.
Idka ständigt förbättringsarbete i alla steg inom verksamhetsområdet.
Samarbeta tvärfunktionellt med personal från produktion-, R&D- och EHS-avdelningarna.
Även arbete i andra projekt rörande miljöfrågor i produktionen för att minska påverkan på yttre miljö.

De huvudsakliga kraven för tjänsten är:
Teknisk högskoleutbildning eller annan relevant utbildning med inriktning mot kemi, bio-/kemiteknik, miljö alternativt motsvarande arbetslivserfarenhet.
Erfarenhet från liknande roll, gärna inom processindustri med teknisk inriktning.
God kommunikationsförmåga samt utmärkta kunskaper i svenska och engelska, såväl muntligt som skriftligt.

Det är även meriterande om du har tidigare erfarenhet av:
Erfarenhet av att driva tekniska projekt inom processrening.
Kunskap om reningsprocesser i storskalig kemisk produktionsverksamhet.

Vi ser gärna att du som söker är driven och ansvarstagande med god förmåga att självständigt kunna ta initiativ och fatta beslut. För att vara framgångsrik i rollen är det även viktigt att du som peär förändringsbenägen, har god problemlösningsförmåga och trivs med att jobba både i grupp och självständigt.
Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag.
#LI-HJ2
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Scientist

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
The Scientist is responsible for application research within the capture field, with focus on monoclonal antibody purification processes. The Scientist is a part of a committed and talented team that are highly involved in new product development. To succeed in this position, you need to be result-oriented, flexible and creative with a strong collaborative attitude, focusing on the customer needs. You are eager to learn and try new things with the drive and capability to initiate, plan, perform, analyze, document and present results.
This position reports to the Senior Manager Capture Application and is part of the Start to Finish department within R&D located in Uppsala and will be an on-site role. We are looking for candidate who can join us after the summer, earliest starting date in July 2025.
What you will do:
As a Scientist you will be part of a team working with different steps in a mAb purification process, i.e. clarification, filtration and purification. Also analysis will be included in your work in our different project types, that is new product development but also market support related activities.
Although most work will be performed at lab scale you will also be involved in harvesting and filtration of feed in larger scale.
The work is independently planned and performed and reported at project meetings and in technical reports.

Who you are:
You have a PhD with some experience from chromatography work in the biopharmaceutical field.
Experienced of using ÄKTA systems and multiple analysis methods (ELISA, SEC and BiaCore).
It’s meritorious if you have worked with large scale purification equipment and processes with mAb or recombinant proteins. Experience of filtration of biomolecules would be appreciated.
Advanced English (oral and writing) and working proficiency in Swedish language.



Travel, Motor Vehicle Record & Physical/Environment Requirements:
Valid Swedish work permit.



Application
We continuously assess candidates and invite them for interviews, so please don’t hesitate to write and send in the application. The recruitment will be completed as soon as a suitable candidate is found.
We look forward to seeing your application. Visa mindre

Systemingenjör

Ansök    Jan 28    Cytiva Sweden AB    Systemansvarig
Bli en del av något helt livsavgörande Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier. Som del av Cytiva kommer du kontinuerligt förbättra dig själv och oss – du kommer att bidra ... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier.
Som del av Cytiva kommer du kontinuerligt förbättra dig själv och oss – du kommer att bidra till att lösa utmaningar som har verklig betydelse för människors hälsa tillsammans med kollegor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i över 40 länder är Cytiva en arbetsplats där varje dag är en möjlighet att lära sig mer – så att du kan fortsätta utvecklas i din karriär och stärka dina färdigheter över tid.
Vi är en del av Danahers bioteknologisegment och sammanför teknisk expertis och talang från hela världen för att utveckla nästa generations livsförändrande terapier.
Vi inom System Support tar ansvar för drift och support av det digitala landskapet inom den kemiska produktionen i Uppsala. Just nu befinner vi oss i en expansion av vår nya digitala plattform som kommer befästa vår världsledande position. Vårt mål är ett landskap där vi till fullo utnyttjar potentialen i vår digitala ryggrad inom produktionen.
Till denna resa stärker vi vårt team med en ny engagerad Systemingenjör.
Teamet ansvarar för ett flertal olika validerade produktionskritiska system. I ansvaret ingår support till användare, systemförvaltning som uppdateringar av system och dokumentation samt deltagande i projekt som subject matter expert. Som systemingenjör är du en viktig del i teamet för att säkra driften och utvecklingen av våra produktionssystem.
Du kommer primärt att arbeta med Snitcher Medical. Ett system vi använder för att utveckla och förvalta etiketter för våra slutprodukter. Det ingår även ansvar för andra system såsom till exempel Boomerang (system för temperaturövervakning).
Vi är mitt i en spännande resa som tar oss in i en digital produktion i världsklass.
I den här rollen kommer du få möjligheten att:
Supportera och utbilda verksamheten samt utföra avhjälpande åtgärder.
Systemförvaltning och uppgraderingar.
Designa och hantera layouter för produktetiketter.
Arbeta med ständiga förbättringar av våra system och interna arbetsprocesser.
Systemintegration.
Upprätthålla systemdokumentation och rutiner

Arbetet är intressant och varierande då du hanterar många ärenden av olika karaktär och kommer i kontakt med många personer både internt och externt. Du ser möjligheter med system som utbyter information i syfte att förenkla, automatisera och säkra kvalitet.
Vi eftersträvar en hög servicegrad varför kommunikation och transparens är viktigt likaså en stor förståelse för våra kunders behov. Självklart sätter du kunden i fokus och är en serviceinriktad person. Det är naturligt för dig att följa upp att pågående aktiviteters levereras samt att tillhörande dokumentation är uppdaterad. Vi ser att du har ett metodiskt arbetssätt och har lätt för att se samband hur olika operationer hänger samman.
De huvudsakliga kraven för tjänsten är:
Examen från högskola eller universitet med relevant inriktning, eller erfarenhet från arbete i liknande roll, eller mångårig erfarenhet som systemingenjör med ansvar för produktionskritiska system.
Ett brinnande intresse för digitalisering.
Erfarenhet från förvaltning av produktionsnära system såsom ERP, MES, asset management eller documentation management. Andra systemerfarenheter är också intressanta.
Livscykelaktiviteter kopplade till system.
Det är naturligt för dig att kommunicera på svenska och engelska.

Det är även meriterande om du har tidigare erfarenhet av:
Systemintegration.
Supportverksamhet och aktiv systemförvaltning.
Produktions IT såsom nätverk, servrar och AD.
Validering av IT system. Visa mindre

Ekonomisk administratör

Ansök    Feb 6    Cytiva Sweden AB    Ekonomiassistent
Bli en del av något helt livsavgörande Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier. På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom at... Visa mer
Bli en del av något helt livsavgörande


Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier.

På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbeta med utmaningar som verkligen spelar roll tillsammans med människor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i 40 länder är Cytiva en plats där varje dag är en möjlighet att lära så att du kan få fart på din karriär och förbättra dina färdigheter på lång sikt.

Vi på Cytiva är stolta över att arbeta tillsammans med en grupp av nio andra Danaher Life Sciences-företag. Tillsammans är vi pionjärer inom vetenskap och medicin och utvecklar produkter som hjälper forskare i kampen att rädda liv.
Som Ekonomisk administratör är du ansvarig för att säkerställa att fastighetsavdelningen har en väl fungerande budget och korrekt ekonomisk uppföljning.
Tjänsten rapporterar till fastighetschefen och är placerad på plats i Uppsala.
Vad du ska göra

· Administrera fastighetsavdelningens budgetarbete
· Uppföljning av budgetutfall och kostnader
· Orderläggning, vara avdelningens sammanhållande resurs / support
· Fakturahantering
· Leverantörskontakt, uppföljning av placerade inköpsorder

Vem du är

· Ekonomisk utbildning eller bakgrund är meriterande
· Vana av att arbeta i en digital värld, hög kunskap i Office-paketet.
· Tålmodig, kommunikativ och lösningsorienterad
· Strukturerad, noggrann och organiserad i ditt arbete
· Vana att arbeta självständigt och samtidigt god förmåga att samarbeta med andra

Vi ser gärna att du som söker denna roll känner igen dig i beskrivningen av en kommunikativ och lösningsorienterad person med högt säkerhetstänk. För att vara framgångsrik i denna roll är det viktigt att du trivs i en verksamhetsnära roll där du får spendera tid på byggplatsen för att kommunicera med utförare.

Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag, söndag 5 mars. För frågor rörande den här tjänsten vänligen kontakta rekryterande chef Tove Kärvin på [email protected]. Varmt välkommen med din ansökan!
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

European Patent Attorney Hardware/Engineering

Ansök    Feb 6    Cytiva Sweden AB    Patentjurist
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
We have an exciting opportunity for a European Patent Attorney (EPA) to work with our expert Intellectual Property team of twentyfive+ employees across the world. The role will be onsite in Uppsala, Sweden and report into Cytiva’s IP Leader for Hardware Solutions.
As a European Patent Attorney, you will be intimately involved in building and implementing the IP strategy for protecting some of Cytiva’s core product portfolios relating to a range of system platforms and software applications for the bioprocess industry. This will cover all aspects from collaborating closely with R&D and business colleagues in building world class IP protection, to execution of global IP litigations. Do you have a passion for innovation and intellectual property? Then we would love to hear from you.
What you’ll do
Lead IP strategy and portfolio management for assigned business areas to ensure that commercially meaningful and enforceable protection is obtained.
Draft and prosecute high quality patent applications.
Perform freedom to operate reviews and minimize exposure to third party IP.
Support IP aspects of business development, licensing, and Merger & Acquisition activities.
Support EPO opposition proceedings and IP enforcement actions.
Provide IP training to R&D, product and marketing teams.

Who you are
Qualified European Patent Attorney
Technical background in mechanical, electrical, or chemical engineering, physics or equivalent.
Excellent written and oral communication skills in English. Proficiency in other languages is considered a plus.
Experience of devising innovative IP strategies.
Good commercial awareness.
Knowledge of laws, regulations, practices and procedures relating to patent procurement in Europe, US and Asia.
Preferably, experience working in the life sciences or healthcare sector.
Valid working permit for Sweden.



Interviews and selection will happen continuously. Welcome in with you application! Visa mindre

Site Service Coordinator

Ansök    Jan 28    Cytiva Sweden AB    Platskoordinator
Bring more to life Är du redo att accelerera din potential och göra verklig skillnad inom biovetenskap, diagnostik och bioteknik? På Cytiva, ett av Danaher’s 15+ operativa företag, räddar vårt arbete liv – och vi är alla förenade av ett gemensamt engagemang för att förnya för påtaglig effekt. Du kommer att trivas i en samhörighetskultur där du och din unika syn är viktig. Och genom att utnyttja Danahers system för ständiga förbättringar hjälper du til... Visa mer
Bring more to life
Är du redo att accelerera din potential och göra verklig skillnad inom biovetenskap, diagnostik och bioteknik?
På Cytiva, ett av Danaher’s 15+ operativa företag, räddar vårt arbete liv – och vi är alla förenade av ett gemensamt engagemang för att förnya för påtaglig effekt.
Du kommer att trivas i en samhörighetskultur där du och din unika syn är viktig. Och genom att utnyttja Danahers system för ständiga förbättringar hjälper du till att omvandla idéer till genomslag – innovativa i livets hastighet.
Att arbeta på Cytiva innebär att ligga i framkant när det gäller att tillhandahålla nya lösningar för att förändra människors hälsa. Våra otroliga kunder genomför livräddande aktiviteter som sträcker sig från grundläggande biologisk forskning till att utveckla innovativa vacciner, nya mediciner och cell- och genterapier.
På Cytiva kommer du att ständigt kunna förbättra dig själv och oss – arbeta med utmaningar som verkligen betyder något med människor som bryr sig om varandra, våra kunder och deras patienter. Ta ditt nästa steg till en helt och hållet livsförändrande karriär.
Lär dig om Danaher Business System som gör allt möjligt.
Site Service Coordinator är ansvarig för att tillhandahålla labrelaterat förbrukningsmaterial inkl service och tjänster kopplat till gas, farligt gods skeppningar samt internorderhantering
Denna position rapporterar till Manager Site Service och är en del av vårt Facility Management team placerad i Uppsala, Sverige och kommer vara en on-site roll.
Vad du ska göra
Serva siten med material/utrustning för laboratorieverksamhet (inkl lagerhållning)
Farligt Gods hantering inkl skeppning farligt gods
Kvävetjänstfyllning NMR & fyllning återvunnet, Pilot Plant
Löpande internorderhantering & registervård av lagersystem
Administrera internrekvisitioner
Etanolredovisning
Bistå Driftcentralen med gas- och inköpsärenden

Vem du är
Dokumenterad erfarenhet av Farligt Gods hantering samt skeppning (IATA, ADR)
Goda kunskaper i svenska och engelska, både tal och skrift
Van datoranvändare med erfarenhet av att arbeta i digitala verktyg och system

Vi ser gärna att du är
Kommunikativ och lösningsorienterad
Säkerhetsmedvetenhet
Har förmåga att bedriva ett organiserat och strukturerat arbete



Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. Varmt välkommen med din ansökan!
Cytiva, ett Danaher-operativt företag, erbjuder ett brett utbud av omfattande, konkurrenskraftiga förmånsprogram som tillför värde till våra liv. Oavsett om det är ett hälsovårdsprogram eller betald ledighet, bidrar våra program till livet utanför jobbet. Kolla in våra förmåner på Danaher Benefits Info. Visa mindre

Senior Optical Engineer

Bli en del av något helt livsavgörande Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier. Som del av Cytiva kommer du kontinuerligt förbättra dig själv och oss – du kommer att bidra ... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier.
Som del av Cytiva kommer du kontinuerligt förbättra dig själv och oss – du kommer att bidra till att lösa utmaningar som har verklig betydelse för människors hälsa tillsammans med kollegor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i över 40 länder är Cytiva en arbetsplats där varje dag är en möjlighet att lära sig mer – så att du kan fortsätta utvecklas i din karriär och stärka dina färdigheter över tid.
Vi är en del av Danahers bioteknologisegment och sammanför teknisk expertis och talang från hela världen för att utveckla nästa generations livsförändrande terapier.
Vi vill nu förstärka vårt team i Uppsala med en optikingenjör. Du kommer ingå i en sektion med andra ingenjörer inom optik, men även inom elektronik och inbyggd mjukvara. Hos oss är tillvaron varierande och du kommer att vara delaktig i utveckling och förbättring av våra kromatografisystem. Du kommer att ha stort ansvar i att själv planera och utföra ditt arbete – frihet under ansvar. Arbetsuppgifterna ger, och behöver, teknisk bredd. Låter detta intressant? Då vill vi höra ifrån dig!
I den här rollen kommer du få möjligheten att:
Designa, utveckla och optimera UV-sensorer och optiska system för kromatografi-applikationer.
Utföra optiksimuleringar och analyser med hjälp av Ansys Zemax OpticStudio för att säkerställa hög prestanda och effektivitet.
Genomföra tester och kalibreringar av optiska system för att säkerställa noggrannhet och tillförlitlighet.
Samarbeta med tvärfunktionella team, inklusive elektronik-, mekanik- och mjukvaruingenjörer, för att integrera optiska komponenter i kompletta system.
Dokumentera designprocesser, testresultat och tekniska specifikationer enligt företagets standarder.
Utföra felsökning och problemlösning av optiska system och komponenter.
Hålla dig uppdaterad med de senaste teknologierna och utvecklingsmetoderna inom optik och sensorteknik.
Bidra till projektplanering och tidsramar genom att uppskatta arbetsinsatser och resurser för optikrelaterade uppgifter.

De huvudsakliga kraven för tjänsten är:
Civilingenjör inom teknisk fysik eller motsvarande.
Mångårig dokumenterad erfarenhet av relaterad produkt- & systemutveckling.
Stark problemlösningsförmåga och förmåga att arbeta i team.
Flytande i svenska och engelska i såväl tal som skrift.

Det är även meriterande om du har tidigare erfarenhet av:
Optik och fotonik med hjälp av modellering och simuleringar.
Spektroskopi och/eller kromatografi. Visa mindre

Embedded Software Engineer

Ansök    Jan 28    Cytiva Sweden AB    Mjukvaruutvecklare
Bli en del av något helt livsavgörande Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier. Som del av Cytiva kommer du kontinuerligt förbättra dig själv och oss – du kommer att bidra ... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier.
Som del av Cytiva kommer du kontinuerligt förbättra dig själv och oss – du kommer att bidra till att lösa utmaningar som har verklig betydelse för människors hälsa tillsammans med kollegor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i över 40 länder är Cytiva en arbetsplats där varje dag är en möjlighet att lära sig mer – så att du kan fortsätta utvecklas i din karriär och stärka dina färdigheter över tid.
Vi är en del av Danahers bioteknologisegment och sammanför teknisk expertis och talang från hela världen för att utveckla nästa generations livsförändrande terapier.
Vi vill nu förstärka vårt team i Uppsala med en mjukvaruutvecklare för inbyggda system. Du kommer ingå i en sektion med ingenjörer inom elektronik, optik och mjukvara inom inbyggda system. Hos oss är tillvaron varierande och du kommer att vara delaktig i utveckling och förbättring av våra kromatografisystem. Du kommer att ha stort ansvar i att själv planera och utföra ditt arbete – frihet under ansvar. Arbetsuppgifterna ger, och behöver, teknisk bredd. Låter detta intressant? Då vill vi höra ifrån dig!
I den här rollen kommer du få möjligheten att:
Designa, utveckla och underhålla inbyggda mjukvarulösningar i C för mikroprocessorer.
Delta i systemarkitektur och designbeslut för nya och befintliga projekt.
Utföra felsökning och korrigering av kod för att säkerställa hög prestanda och tillförlitlighet.
Samarbeta med hårdvaruingenjörer för att integrera och verifiera mjukvara med hårdvarukomponenter.
Dokumentera kod, utvecklingsprocesser och tekniska specifikationer enligt företagets standarder.
Delta i och bidra till kodgranskningar för att säkerställa kodkvalitet och efterlevnad av guidelines.
Hålla dig uppdaterad med de senaste teknologierna och utvecklingsmetoderna inom inbyggda system.

De huvudsakliga kraven för tjänsten är:
Civil- eller högskoleingenjör inom elektronik, datateknik, teknisk fysik eller liknande.
1+ års dokumenterad erfarenhet av mjukvaruutveckling för inbyggda system.
Stark problemlösningsförmåga och förmåga att arbeta i team.
Flytande i svenska och engelska i såväl tal som skrift.

Det är även meriterande om du har tidigare erfarenhet av:
IAR:s utvecklingsmiljö och kompilator.
Git och Azure DevOps. Visa mindre

Cyber Security Engineer

Ansök    Jan 23    Cytiva Sweden AB    Dataingenjör
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
As Cyber Security Engineer within the department you will collaborate with other engineers trained in the field to support life cycle management of legacy products and the development of new products. You will work with the team to create threat models, assess vulnerabilities and together with stakeholders such as product managers decide and execute actions as appropriate.
The role needs to work very horizontal both within R&D and outside with other functions such as service and product management.
This position reports to Sr Manager Magnus Emerius and is part of the ÄKTA Instrument Engineering Section under the Systems Department at R&D located in Uppsala, Sweden and will be an on-site role.
What you will do:
Ensure our products comply with new Information Security standards and frameworks, and best practices for product security, such as NIST SP 800-53 and IEC 62443.
Work with incident response investigations, corrective actions, and preventive actions.
Design of secure systems including secure solutions for embedded software.
Ensure secure configuration, installation and deployment for Windows and Linux.
Threat modelling based on STRIDE.

Who you are:
Master’s degree in engineering or technical discipline or equivalent experience.
Documented education or training in the field of cyber security, or equivalent experience.
Experience from working with threat modelling and risk analysis.
At least 3-5 years of experience working with system development/R&D.
Fluent in Swedish and English, both verbally and in writing.

Application
We continuously assess candidates and invite them for interviews, so please don’t hesitate to write and send in the application before the 14th of February 2025. However the position is filled as soon as we find a suitable candidate.
We thank you for your interest and look forward receiving your application. Visa mindre

EHS Director

Ansök    Jan 28    Cytiva Sweden AB    Miljöchef
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ide... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
We are currently looking for an experienced Environment, Health & Safety (EHS) Director to join us in our mission to advance and accelerate therapeutics at our chemical manufacturing site in Uppsala. As EHS Director at Cytiva, you will play a key role in ensuring the highest standards of safety, health and environmental practices across our Uppsala operations by leading a team of 18 EHS expert professionals within Process Safety, Work Environment, Occupational Health and Environment. The EHS Director role is a senior management position reporting directly to the Managing Director and interfaces with both Global EHS Leadership, Site Leadership as well as the local Crisis Management team.
What you'll do:
Manage the development, implementation, and maintenance of environmental, health, and safety (EHS) programs to ensure compliance, injury prevention, and risk mitigation at the local level.
Partner with Cytiva site leaders to continuously improve the safety culture, awareness, and accountability in support of EHS programs.
Drive the implementation of Danaher's framework for continuous improvements (DBS).
Interface with site EHS committees, as well as the Emergency Response and Crisis Management teams.
Evaluate proposed EHS compliance laws and regulations to determine impact to compliance programs and business operations.
Interpret laws and regulations to determine applicability for facilities of responsibility and implement programs to comply.
Implement EHS management systems programs and associated documentation.
Complete audits, IH sampling, ergonomic assessments, and assists in pollution prevention activities.

Who you are:
MSc Degree within Chemical Engineering, Environmental Engineering, or equivalent.
Demonstrated leadership capabilities and a keen interest in people management.
Several years of management experience in a manufacturing setting, preferably chemical industry or related.
Demonstrated ability to drive EHS-related projects.
Sound knowledge of process- and construction safety.
Fluency in both Swedish and English is required.

It would be a plus if you also possess previous experience in:
Strong knowledge of both local and international EHS regulations, standards and best practices.
Experience leading ISO 14001, 9001 and/or 13485 certification processes.

The candidate we’re looking for has a team-oriented leadership style with excellent communication and interpersonal skills to embrace change and ability to manoeuvre in a fast-paced and unambiguous environment. To be successful in this role, we believe that the candidate should be highly structured, well-organized and demonstrate strong personal integrity and high ethical standards.
Interview and selection will happen continuously, and the opening can be filled before last day of application. For any questions regarding this position, please reach out to Inga Ljung, Managing Director & Site Leader, [email protected] or Hampus Jendle, Talent Acquisition Advisor, [email protected]. We look forward to hearing from you! Visa mindre

Produktionsplanerare

Bli en del av något helt livsavgörande Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier. På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbe... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier.
På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbeta med utmaningar som verkligen spelar roll tillsammans med människor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i 40 länder är Cytiva en plats där varje dag är en möjlighet att lära så att du kan få fart på din karriär och förbättra dina färdigheter på lång sikt.
Vi på Cytiva är stolta över att arbeta tillsammans med en grupp av nio andra Danaher Life Sciences-företag. Tillsammans är vi pionjärer inom vetenskap och medicin och utvecklar produkter som hjälper forskare i kampen att rädda liv.
Vi söker nu en produktionsplanerare till vår kemiska produktionssite i Uppsala. Som produktionsplanerare hos oss ansvarar du för att sätta produktionsplanen, tillse att material finns tillgängligt för produktionen samt följa upp leveranserna. I rollen ingår även att optimera lager och kapacitetsutnyttjande, vilket ofta drivs i mindre arbetsprojekt. Arbetet förutsätter ett tätt samarbete med många kontaktytor inom såväl produktion, distribution samt marketing, vilket ställer höga krav på noggrannhet, struktur och kommunikativ förmåga.
Vad du ska göra
Hos oss får du möjligheten att arbeta både operativt och strategiskt där ständiga förbättringar välkomnas. Du planerar produktionen i nära samarbete med olika avdelningar.
Skapa produktionsplan för fabriken.
Leda planeringsmöten.
Arbeta med lagerstyrning och optimering.
Ansvara för tilldelning av material.
Arbeta med att förbättra och effektivisera processer.
Följa upp utfallet mot produktionsplanen.

På Cytiva finns goda möjligheter till karriärutveckling och tjänsten kan på sikt utvecklas och formas utifrån din bakgrund och intresseområde.
Vem du är
Vi tror att du har en Ingenjörs eller Civilingenjörsutbildning inom logistik eller teknik eller motsvarande.
Du har erfarenhet av produktionsplanering inom tillverkningsindustrin.
Erfarenhet av ERP-system och goda kunskaper i Excel.
Goda kunskaper i svenska och engelska såväl tal som skrift.
En förmåga att leda och inspirera andra människor.
Du har en serviceinriktad attityd och ett effektivt arbetssätt.
Du har en mycket god kommunikativ förmåga. Visa mindre

Energicontroller

Ansök    Jan 17    Cytiva Sweden AB    Controller
Bli en del av något helt livsavgörande Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier. Som del av Cytiva får du möjlighet att utveckla dig själv och oss – du kommer att bidra till... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier.
Som del av Cytiva får du möjlighet att utveckla dig själv och oss – du kommer att bidra till att lösa utmaningar som har verklig betydelse för människors hälsa tillsammans med kollegor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i över 40 länder är Cytiva en arbetsplats där varje dag är en möjlighet att lära sig mer – så att du kan fortsätta växa i din karriär och stärka dina färdigheter över tid.
I rollen som Energicontroller blir du en del av Infrastructure Supply på Cytivas site i Uppsala. Som energicontroller spelar du en avgörande roll i arbetet kring att Cytiva skall gå i förgrunden för en hållbar energianvändning och resurseffektiv industri. Du kommer att ha en viktig roll i att följa, analysera och utmana vårt hållbarhetsarbete. Vi har antagit ambitiösa mål för CO2-fotavtryck och har ett flertal spännande projekt som vi vill realisera för att nå dessa mål. Rollen kommer att ha ett upplägg där man på daglig basis jobbar 5 dagar i veckan onsite.
Dina arbetsuppgifter:
Ansvara för den strategiska CO2 planen för att nå sitens åtaganden och mål. Delta i analyser av projekt och påverka investeringar ur ett hållbarhetsperspektiv.
Följa sitens energiprestanda och dess finansiella effekter. Rapportera dessa till ledning och andra intressenter.
Driva rapportering av energinyckeltal på miljökommitté. Analysera nyckeltalens effekt och driva framtagandet av nya.
Vara bolagets kompetens inom energikartläggning samt tillhörande styrsystem (tex ISO 50001). Övervaka myndigheter samt intresseorganisationers ambitioner inom hållbarhet

De huvudsakliga kraven för tjänsten är:
Du har en akademisk examen minst 3 år inom naturvetenskapligt område eller motsvarande arbetslivserfarenhet inom industri i kombination med hållbarhetsarbete.
Du behärskar svenska och engelska flytande i tal och skrift.
Du har goda kunskaper i ordbehandlings-, kalkyl- och presentationsprogram, e-posthantering samt internetanvändning kopplat till yrkesområdet.
Du har dokumenterad kunskap i svensk miljölagstiftning eller Agenda 2030 eller hållbarhetsrapportering.

Det är även meriterande om du har:
Om du har erfarenhet av omvärldsbevakning både nationellt och internationellt. Såväl lagrummet som teknisk utveckling.
Om du har god kommunikativ förmåga och trivs med att saluföra din ideér
Om du kan definiera finansiella nyckeltal för energiuppföljning och resurseffektivitet eller är certifierad energikartläggare.
Har erfarenhet av olika industrier eller myndigheter.

Intervjuer och urval sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. Vi råder er därav att ej vänta med er ansöka, utan hoppas vi ses vid en framtida intervju. Visa mindre

Team Lead Hardware

Ansök    Jan 21    Cytiva Sweden AB    Hårdvarukonstruktör
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
We are looking for an engaged Team Lead to join the Hardware Engineering section within the Downstream Hardware R&D organization.
The Hardware Engineering section of Downstream R&D consist of many experienced engineers and together we develop the next generation of products for research and large-scale manufacturing of pharmaceuticals and vaccines. In our development, we use modern development tools, Creo for 3D CAD, Ansys for FEA/CFD calculations/simulations. We focus on modern technology such as 3D printing, laser welding, and bonding. We have access to a prototype workshop with the latest 3D printers for plastic and metal, equipment for laser welding and plastic bonding, as well as CNC machines for machining
What You'll Do
Lead and coordinate tasks for a team of approximately 10 engineers specializing in mechanics, electronics, optics, embedded systems, and testing.
Ensure that product designs meet project goals for efficient transfer to production and service.
Develop and enhance our working methods in collaboration with teams and other team leaders.
Guide your team in developing systems that include pumps, valves, robotics, and more.

Who You Are
Bachelor's degree in mechanical engineering or similar relevant field, combined with several years working experience.
Proven leadership experience in an engineering environment.
Strong engineering background with extensive knowledge in multiple engineering disciplines.
Ability to foster a collaborative and productive team environment.
Experience in system development projects is a plus.
Proficient in both English and Swedish. Visa mindre

Teknisk Service Projektingenjör/Service Upgrade Engineer

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
As a result of our growing customer needs to ensure maximum lifecycle utilization of their equipment, we are looking for a Global Services Upgrade Engineer/ Technical Services Project Engineer.
The Global Services Upgrade Engineer will be responsible for managing custom upgrade orders. This includes reviewing order, creating part numbers and a build of materials, sourcing the material, engineering the upgrade, and putting instructions together on how to execute the upgrade in the field.
This position reports to the Sr Manager,Global Services Custom Products and Repair Center Operations and is part of the Customer Support Multifuction department located in either Uppsala or Umeå, Sweden and will be an on-site role.
What you’ll do:
Review customer orders for upgrades and determine whether the upgrade is possible.
Create a quote and price proposal to customer
Put together a build of materials for each upgrade and sending a quotation to the requester for the upgrade.
Manage the upgrade projects through installation and making sure the projects runs smoothly.
Maintain appropriate relationships and work with both internal and external suppliers to get pricing and material for each upgrade.
Assemble and quality check each upgrade before sending to the customer.
Write any needed documentation for the field team to execute the upgrade at the customer site.
Handle any customer complaints which come in regarding upgrades delivered.
Work closely with our manufacturing and align resources needed to deliver upgrades.
Ensure regular communication to key stakeholders and end users (Service Managers/Field Engineers)
Develop and maintain quality-controlled processes/SOPs
Upgrade support to customer and field engineer, travel as needed – 10-15%.

Who you are:
High level of technical knowledge and understanding (hardware/software)
Bachelor of Science/ Engineering or equivalent
5--10 years experience with electrical and automation design and/or in similar role
Strong focus on customer, quality and meeting customer needs in a global environment
Excellent communications skills in Swedish and English (oral and written)
Proficient in Microsoft Office applications

Interviews and candidate selection will happen continuously, we look forward to your application today!
Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. Visa mindre

Software Engineer

Ansök    Jan 14    Cytiva Sweden AB    Mjukvaruutvecklare
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas ... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
We're currently looking for our next Software Engineer to join our Global Service R&D Organization located in Uppsala, Sweden. As Software Engineer at Cytiva, you will be responsible for Design and Development of Service Platform & Products to enable remote troubleshooting and diagnostics. The position is an onsite role based at Cytiva's facilities in Uppsala and will report to the Senior Engineering Manager, Service R&D.
In this role, you will have the opportunity to:
Write C#.NET to develop Windows Services that meets standards and delivers desired functionality for the project.
Apply principles of SDLC and Lean/Agile/XP/TDD/CI/CD methodologies to deliver high quality, secured, and scalable software modules.
Write Angular, HTML, Javascript code on .NET core/framework including REST APIs to develop Web Services that meets standards and delivers desired functionality for the project.
Use cloud technologies (Azure, AWS) and/or WCF.
Evaluate basic technology choices and eloquent trade-offs.
Use Multithreading approach to achieve performance.
Optimizing existing and ongoing Application for improved performance, scalability, and efficiency.
Contributing to the establishment of best practices and standards for software development within the organization.
Support team members through pair programming and code reviews.

The essential requirements of the job include:
Degree in Computer Science or Software Engineering (or equivalent qualification).
Proficient in C#/HTML/Angular/JS on .NET core/framework.
Skilled in Azure DevOps Repos/Pipelines to enable incremental software development.
Experience with SDK or software platform development and supporting product-based variability.
Exposure to InstallShield to run installation upgrades during consecutive releases.
Exposure to Continuous Integration, delivery and deployment, version Control.
Can deliver without supervision and know when to seek help.
Ability to work with multi-functional, global and remote teams.

It would be a plus if you also possess previous experience in:
Biotechnology/Life Sciences industry.
GMP & regulatory environments.
QMS and Documentation Practices.

Interview and selection will happen continuously and the opening can be filled before last day of application. For questions regarding the role please contact hiring manager Manoja Prabhu, Sr Engineering Manager - Service R&D, at [email protected]. We look forward to hearing from you!
#LI-HJ2
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Global Repair, Parts & Tools Engineer

Bli en del av något helt livsavgörande Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier. Som del av Cytiva kommer du kontinuerligt förbättra dig själv och oss – du kommer att bidra ... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier.
Som del av Cytiva kommer du kontinuerligt förbättra dig själv och oss – du kommer att bidra till att lösa utmaningar som har verklig betydelse för människors hälsa tillsammans med kollegor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i över 40 länder är Cytiva en arbetsplats där varje dag är en möjlighet att lära sig mer – så att du kan fortsätta utvecklas i din karriär och stärka dina färdigheter över tid.
Vi är en del av Danahers bioteknologisegment och sammanför teknisk expertis och talang från hela världen för att utveckla nästa generations livsförändrande terapier.
Vi söker nu en person till rollen som Remanufacturing/Repair Shop Engineer till gruppen Global Service Center på Cytivas site i Umeå. Vi är ett team på 9 personer som arbetar med renovering av hela instrument och dess reservdelar. I arbetet med renovering ingår felsökning, demontering, montering samt test. Utöver detta arbetar gruppen med att bistå Cytivas fältingenjörer med kalibrering av verktyg, kontroll av reservdelar och även utföra service av hela instrument. Tjänsten är helt on site.
I den här rollen kommer du få möjligheten att:
Kvalitetskontroll och paketering av reservdelar (Spare parts return processen)
Supportera serviceavdelningen med administration kring inköp, bokningar, skeppning och orderläggning med mera.
Logistikhantering.
Vara delaktig i den dagliga planeringen inom gruppen, hålla ordning och reda, utveckla arbetsmetoder samt följa gällande lagar, regler och policys.

De huvudsakliga kraven för tjänsten är:
3-årig gymnasial utbildning eller minst 2 års erfarenhet av order- och logistikhantering inom tillverkningsindustri.
Erfarenhet av operativt arbete rörande order- och logistikhantering.
Lagspelare med god samarbetsförmåga och vana av att jobba både med teknik och människor.
Goda kunskaper i svenska och engelska, såväl muntligt som skriftligt.

Det är även meriterande om du har tidigare erfarenhet av:
Att tidigare arbetat med bokningar, skeppning och orderläggning
Att arbeta i Magic, Oracle och ServiceMax/Salesforce Visa mindre

Scientist - Protein Analysis

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas ... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
We are currently looking for a Scientist to join our Affinity Ligand characterization team within the R&D Resins and Technologies Business Unit at Cytiva. The team is responsible for development of analytical methods to characterize biomolecules such as new protein ligands and target molecules such as mAbs. The team is also responsible for method validation and transfer to QC. This position is based in Uppsala, Sweden and will be an on-site role.
What you will do:
Plan, perform, document and present laboratory experiments. The work includes analysis of affinity ligands, mAbs and antibody fragments.
Provide technical expertise within the areas of protein analysis. Solve technical problems, supporting both Research and Development projects for novel affinity ligands.
Act as a mentor/local expert and support peers with analysis of a wide range of proteins.
Present scientific and technical results internally and externally, oral and written communication in English and Swedish.

The essential requirements of the job include:
5-years experience from industrial work or PhD in Microbiology/Biochemistry or related Life Science field.
Experience of analysis of proteins with focus on HPLC and LC-MS.
Experience from analytical method transfers from R&D to QC.
English and Swedish as working languages.

It would be a plus if you also have:
Experience working with methods used in analysis of proteins such as Biacore.
Sound knowledge of protein purification.

The ideal candidate is a result-oriented, flexible, and creative individual with a strong collaborative attitude. To succeed in this role, the ideal candidate should also be quality-focused, precise, and capable of working in a structured manner.
Interview and selection will happen continuously, and the opening can be filled before last day of application. For questions regarding the role please contact hiring manager Johanna Tschöp, Senior Manager - Affinity Ligand Characterization, [email protected]. Welcome in with your application!
#LI-HJ2
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Software Engineer

Ansök    Jan 8    Cytiva Sweden AB    Mjukvaruutvecklare
Bli en del av något helt livsavgörande Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier. Som del av Cytiva kommer du kontinuerligt förbättra dig själv och oss – du kommer att bidra... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier.
Som del av Cytiva kommer du kontinuerligt förbättra dig själv och oss – du kommer att bidra till att lösa utmaningar som har verklig betydelse för människors hälsa tillsammans med kollegor som bryr sig om varandra, våra kunder och deras patienter.
Med medarbetare i över 40 länder är Cytiva en arbetsplats där varje dag är en möjlighet att lära sig mer – så att du kan fortsätta utvecklas i din karriär och stärka dina färdigheter över tid.
Vi söker nu efter en Software Engineer till ett av våra mjukvaruutvecklingsteam inom avdelningen R&D BioProcess Software på Cytiva i Uppsala. Avdelningen består idag av ett 90-tal medarbetare som ansvarar för mjukvaruutvecklingen inom området BioProcess Downstream. Vår största mjukvara, UNICORN, används av kromatografi-, cellodling- och filtreringsystem för styrning, övervakning och avancerad analys.
I rollen som Software Engineer ansvarar du tillsammans med dina teammedlemar för design, dokumentation, implementation och verifiering av mjukvara i en agil utvecklingsmiljö. Du ansvarar för att färdigställa features enligt teamets framtagna tidplan där arbetet sker i prioritetsordning och uppgifterna hämtas från teamets backlog. Tjänsten har placering on-site i Uppsala.
Dina arbetsuppgifter:
Planera och utveckla nya features till våra produkter samt genomföra tekniska utredningar.
Skriva teknisk dokumentation så som design-, krav-, och testspecifikationer.
Underhålla befintliga produkter.
Stötta vårt kundsupportteam med teknisk kompetens om våra produkter samt att ingå i tekniska utredningar av kundproblem vid behov.

De huvudsakliga kraven för tjänsten är:
Relevant universitetsutbildning, exempelvis MSc / BSc Software Engineering, Computer Science, eller motsvarande.
Erfarenhet av mjukvaruutveckling med tonvikt på C# / .NET.
Du kommunicerar flytande på både svenska och engelska.

Det är även meriterande om du har:
Erfarenhet av TDD (Test Driven Design) och BDD (Behavior Driven Design).
Erfarenhet av produktutveckling och kunskap om produktslivscykeln.
Vana att jobba inom ett kvalitetssystem.
Erfarenhet av agila arbetsmetoder.

Stor vikt kommer att läggas vid den ansökandes personlighet, professionella intressen och driv.?Vi söker dig som är driven och som inspireras av nya utmaningar, är prestigelös och har intresse för ny teknik. Du är trygg i din tekniska kompetens, delar med dig av idéer och samarbetar med andra på ett bra sätt för att nå de bästa lösningarna.
Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. För frågor rörande tjänsten vänligen kontakta rekryterande chef Frederik Isacsson, Senior Manager - Lab Instrument Software & CCM, [email protected]. Välkommen med din ansökan! Visa mindre

Software Engineer / Frontend Developer

Ansök    Jan 9    Cytiva Sweden AB    Frontend-utvecklare
Bli en del av något helt livsavgörande Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier. Som del av Cytiva kommer du kontinuerligt förbättra dig själv och oss – du kommer att bidra... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier.
Som del av Cytiva kommer du kontinuerligt förbättra dig själv och oss – du kommer att bidra till att lösa utmaningar som har verklig betydelse för människors hälsa tillsammans med kollegor som bryr sig om varandra, våra kunder och deras patienter.
Med medarbetare i över 40 länder är Cytiva en arbetsplats där varje dag är en möjlighet att lära sig mer – så att du kan fortsätta utvecklas i din karriär och stärka dina färdigheter över tid.
Vi söker nu efter en Software Engineer med erfarenhet av Frontendutveckling till ett av våra mjukvaruutvecklingsteam inom avdelningen R&D BioProcess Software på Cytiva i Uppsala. Avdelningen består idag av ett 90-tal medarbetare som ansvarar för mjukvaruutvecklingen inom affärsområdet BioProcess Downstream. Vår största mjukvara, UNICORN, används av kromatografi-, cellodling- och filtreringsystem för styrning, övervakning och avancerad analys.
I rollen som Software Engineer kommer du att jobba i en dynamisk och agil miljö där du kommer vara en del av ett team involverat i hela utvecklingsprocessen från kravspecificering till implementation och test samt slutligen verifiering. Automatiserad enhetstestning, TDD (Test Driven Design) och BDD (Behavior Driven Design) är en integrerad del av arbetssättet. Tjänsten har placering on-site i Uppsala.
Dina arbetsuppgifter:
Planera och utveckla nya features till våra produkter samt genomföra tekniska utredningar.
Skriva teknisk dokumentation så som mjukvarudesign-, krav- och testspecifikationer.
Underhålla befintliga produkter.
Stötta vårt kundsupportteam med teknisk kompetens om våra produkter samt att ibland ingå i tekniska utredningar av kundproblem.

De huvudsakliga kraven för tjänsten är:
Relevant universitetsutbildning, exempelvis MSc / BSc Software Engineering, Computer Science, eller motsvarande.
Erfarenhet av mjukvaruutveckling med tonvikt på C# / .NET samt WPF / Win Forms.
Vana att jobba inom ett kvalitetssystem.
Du kommunicerar flytande på både svenska och engelska.

Det är även meriterande om du har:
Erfarenhet av TDD (Test Driven Design) och BDD (Behavior Driven Design).
Erfarenhet av produktutveckling och kunskap om produktlivscykeln.
Vana att jobba inom ett kvalitetssystem.
Erfarenhet av agila arbetsmetoder.
Intresse för cyber security och secure coding.

Stor vikt kommer att läggas vid den ansökandes personlighet, professionella intressen och driv.?Vi söker dig som har god analytisk förmåga och ett stort intresse för mjukvaruutveckling. Du är trygg både i din tekniska kompetens och känner dig bekväm i att samarbeta brett och tvärfunktionellt med andra för att hitta lösningar och nå resultat.
Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. För frågor rörande tjänsten vänligen kontakta rekryterande chef Ulrika Öhman, Senior Manager - UNICORN Application Software, [email protected]. Välkommen med din ansökan! Visa mindre

Lead System Engineer

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
We're looking for a Lead System Designer to join our Custom Engineering department at Cytiva in Uppsala. This position reports to the Sr Manager for Functional Design and will be an on-site role.
As Lead System Designer at Custom Engineering you will be working primarily on customized customer projects together with cross-functional project teams consisting of 8 to 10 people. Each project typically lasts between 6-12 months. In this role, you will take responsibility for the functionality and quality of the customized bioprocess product, including specifications, component and equipment selection as well as regulatory compliance. Your daily activities will be to work closely with the other design disciplines (Mechanical, Automation and Electrical Design Engineering) to ensure that all customer requirements are captured and implemented into the product. At the end of the project, the customer will perform an acceptance test of the equipment at our facility where you will represent the design team and support the customer with technical knowledge.
Cytivas customers are based across the globe, and a few business trips per year may be required as well as some early or late conference calls depending on projects and region.
What You'll Do:
Read customer specifications and translate these into specifications and designs.
Perform design reviews internally and externally together with the customer.
Coordinate design activities between functions (Mechanical, Electrical and Automation design).
Ensure regulatory compliance of your products.
Act as a support function for Service, Manufacturing and Verification.

Who you are:
This position requires an MSc or BSc in Engineering, Physics or Biotechnology, or equivalent.
You have several years of documented experience from working with product development or process development within a regulatory controlled industry or environment.
Experience in performing and/or leading technical investigations and reports (CAPA investigations, component evaluations, etc).
Fluency in English, both written and oral is a requirement. Fluency in Swedish is an advantage.

It would be a plus if you also possess previous experience in:
Knowledge of project management techniques and models.
Experience from technical roles within the Life Science industry.
Experience from working in PDM system.

To be successful in this role, you should have a deep-rooted technical interest, strong quality-focus, and enjoy working in smaller project teams. Excellent communication skills are essential, and you should be comfortable presenting technical solutions to customers.
Interview and selection will happen continuously and an opening can be filled before last day of application. For questions and more information about the role please contact hiring manager Joakim Eklund, Sr Manager - Functional Design, [email protected].
#LI-HJ2
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Bioprocess Development Scientist

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas ... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible.
The Bioprocess Development Scientist is responsible for evaluating and optimizing Cytiva filtration technology in biopharmaceutical processes. The BDS advises customers on process options, runs filterability studies, and helps overcome filtration challenges in drug process development. This position is located remotely in Uppsala, Sweden and covers projects in the Nordics and Baltics territory. This position reports to the EMEA Filtration BPS Leader and is part of the BioPharma Process team and will be fully remote.


What you will do:
Engage in technical consultations with customers on downstream filtration processing where you evaluate and propose options for process optimization
Coordinate, perform and analyze bench scale test work at customer site for Cytiva filtration technologies in customer’s biopharmaceutical processes.
Serve as a technical specialist with in-depth knowledge of Cytiva products and downstream processing and develop expertise by regular exchange of experiences and trainings.
Join a dynamic cross-functional and cross-regional team of bioprocess scientists
Work in close relationship with sales specialists, account managers, and scientists to coordinate activities and win sales
Be part of the bringing future biopharmaceuticals to patients by supporting process development of molecules such as monoclonal antibodies, recombinant proteins or vaccines



Who you are:
Master’s Degree in Life Science, Chemical or Biological, or Engineering or related field required, PhD preferred
5 plus years of relevant experience in biotech industry, preferably in downstream process development
Valid driver’s license
Willing to travel regionally (approximately 50%) with occasional travel outside assigned territory
English fluency required, Swedish language a plus Visa mindre

Software Development Manager

Ansök    Dec 25    Cytiva Sweden AB    Utvecklingschef
Be part of something altogether life-changing! Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that trul... Visa mer
Be part of something altogether life-changing!
Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
At Cytiva, our software products are essential cornerstones for the success of our BioPharma instruments. Currently, we are looking for our next Section Manager to lead our one of our UNICORN Software development sections consisting of 15 employees in Uppsala. Together with the other 4 software development sections across the Downstream Software department, the UNICORN Software development teams work together to develop and maintain the software products for our ÄKTA portfolio, including control software and the UNICORN software application.
As the Section Manager for the UNICORN Software development team, you will manage the software development activities in collaboration with the Hardware and System & Application teams as well as product management and other internal stakeholders. You will also play a key role in driving changes to improve efficiency in the software development work.
What you’ll do:
Lead, support and develop your team, and manage activities to fulfil short- and long-term organizational goals and priorities.
Participate in the Downstream Software Department’s Management Team and contribute to the department’s overall mission, i.e. software development, product care and support of our software products for the ÄKTA chromatography systems.
Together with your team and other functions in the UNICORN product development, drive the software development related strategy in line with the business and architectural needs.
Work to ensure cross collaboration within the Downstream R&D Software department, as well as externally towards other software developing organizations within Cytiva and continuously improve our common ways of working.
Contribute in driving the evolution of software development for life changing therapeutics.

The essential requirements of the job include:
MSc or similar education in the software development field.
Rich experience in relevant software and system product development.
Experience in the development of software for regulated industries, such as biopharma or medical devices is an advantage.
Proven leadership and people management skills with experience from line management or project management.
Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.
Genuine interest in developing both people and software solutions.
Fluency in both Swedish and English is required.

It would be a plus if you also possess previous experience in:
Knowledge of lean methodologies and agile development frameworks.
Experience working with UNICORN software.

Interview and selection will happen continuously, and the opening can be filled before last day of application. For questions regarding the role please contact hiring manager Åsa Nordstedt at [email protected]. We look forward to hearing from you!
#LI-HJ2
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Senior Software Engineer

Ansök    Jan 8    Cytiva Sweden AB    Mjukvaruutvecklare
Bli en del av något helt livsavgörande Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier. Som del av Cytiva kommer du kontinuerligt förbättra dig själv och oss – du kommer att bidra... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier.
Som del av Cytiva kommer du kontinuerligt förbättra dig själv och oss – du kommer att bidra till att lösa utmaningar som har verklig betydelse för människors hälsa tillsammans med kollegor som bryr sig om varandra, våra kunder och deras patienter.
Med medarbetare i över 40 länder är Cytiva en arbetsplats där varje dag är en möjlighet att lära sig mer – så att du kan fortsätta utvecklas i din karriär och stärka dina färdigheter över tid.
Vi söker nu efter en Senior Software Engineer till ett av våra mjukvaruutvecklingsteam inom avdelningen R&D BioProcess Software på Cytiva i Uppsala. Avdelningen består idag av ett 90-tal medarbetare som ansvarar för mjukvaruutvecklingen inom området BioProcess Downstream. Vår största mjukvara, UNICORN, används av kromatografi-, cellodling- och filtreringsystem för styrning, övervakning och avancerad analys.
I rollen som Senior Software Engineer ansvarar du tillsammans med dina teammedlemar för design, dokumentation, implementation och verifiering av mjukvara i en agil utvecklingsmiljö. Du ansvarar för att färdigställa features enligt teamets framtagna tidplan där arbetet sker i prioritetsordning och uppgifterna hämtas från teamets backlog. Tjänsten har placering on-site i Uppsala.
Dina arbetsuppgifter:
Planera och utveckla nya features till våra produkter samt genomföra tekniska utredningar.
Skriva teknisk dokumentation så som design-, krav-, och testspecifikationer.
Underhålla befintliga produkter.
Stötta vårt kundsupportteam med teknisk kompetens om våra produkter samt att leda tekniska utredningar av kundproblem vid behov.

De huvudsakliga kraven för tjänsten är:
Relevant universitetsutbildning, exempelvis MSc / BSc Software Engineering, Computer Science, eller motsvarande.
Flerårig erfarenhet av mjukvaruutveckling med tonvikt på C#/.NET.
Kommunicerar flytande på både svenska och engelska.

Det är även meriterande om du har:
Erfarenhet av TDD (Test Driven Design) och BDD (Behavior Driven Design).
Erfarenhet av produktutveckling och kunskap om produktslivscykeln.
Vana att jobba inom ett kvalitetssystem.
Erfarenhet av agila arbetsmetoder.

Stor vikt kommer att läggas vid den ansökandes personlighet, professionella intressen och driv.?Vi söker dig som är driven och som inspireras av nya utmaningar, är prestigelös och har intresse för ny teknik. Du är trygg i din tekniska kompetens, delar med dig av idéer och samarbetar med andra på ett bra sätt för att nå de bästa lösningarna.
Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. För frågor rörande tjänsten vänligen kontakta rekryterande chef Frederik Isacsson, Senior Manager - Lab Instrument Software & CCM, [email protected]. Välkommen med din ansökan! Visa mindre

Senior QA Engineer - Projects

Bli en del av något helt livsavgörande Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier. På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbe... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier.
På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbeta med utmaningar som verkligen spelar roll tillsammans med människor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i 40 länder är Cytiva en plats där varje dag är en möjlighet att lära så att du kan få fart på din karriär och förbättra dina färdigheter på lång sikt.
Vi på Cytiva är stolta över att arbeta tillsammans med en grupp av nio andra Danaher Life Sciences-företag. Tillsammans är vi pionjärer inom vetenskap och medicin och utvecklar produkter som hjälper forskare i kampen att rädda liv.
Nu söker vi en Senior QA Engineer - Projects till sektionen QA Projects på Cytivas QA avdelning i Uppsala. Som Senior QA Engineer representerar du QA i R&D- och siteprojekt med särskilt fokus på valideringsaktiviteter. I denna roll jobbar du tvärfunktionellt tillsammans med medarbetare från bland annat produktion, R&D och PMO. Tjänsten är en onsiteroll med placering i Uppsala.
I den här rollen får du möjlighet att:
Representera QA i tvärfunktionella projekt som nyprodukt- och utrustningsprojekt.
Bidra till att valideringsaktiviteter blir färdigställda inom satta tidsplaner, i nära samarbete med övriga funktioner.
Representera QA i tvärfunktionella riskanalyser.
Remissa och godkänna riskanalyser, valideringsdokumentation och avvikelser.
Aktivt delta i och driva förändringsarbete och ständiga förbättringar inom projekt och processer.
Säkerställa efterlevnad av vårt kvalitetssystem (QMS) i nära samarbete med övriga organisationen.

Grundläggande krav för tjänsten är:
Högskoleutbildning inom kemi, farmaci eller motsvarande.
Flerårig erfarenhet från liknande QA-roller inom reglerad Life Sciencesverksamhet (t.ex ISO 9001, ISO 13485 och/eller GMP).
Erfarenhet av att representera QA i projekt.
Goda kunskaper om validering- och kvalificeringsaktiviteter inom automation, processutrustning och CSV.
Erfarenhet av att driva och/eller representera QA i riskanalyser.
Erfarenhet av att driva och/eller representera QA i avvikelseutredningar.
Du kommunicerar flytande på svenska och engelska i både tal och skrift.

Det är även meriterande om du har:
Goda kunskaper om riskanalysmetodiker.
Erfarenhet av komplexa QA projekt och aktiviteter

Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. För frågor relaterade till tjänsten kontakta rekryterande chef Erika Lodén, Section Manager QA - Projects, [email protected]. Visa mindre

Sektionschef - Produktion, Biacore

Bli en del av något helt livsavgörande Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier. Som del av Cytiva får du möjlighet att utveckla dig själv och oss – du kommer att bidra ti... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier.
Som del av Cytiva får du möjlighet att utveckla dig själv och oss – du kommer att bidra till att lösa utmaningar som har verklig betydelse för människors hälsa tillsammans med kollegor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i över 40 länder är Cytiva en arbetsplats där varje dag är en möjlighet att lära sig mer – så att du kan fortsätta växa i din karriär och stärka dina färdigheter över tid.
Vi söker nu efter en chef till sektionen Biacore på Cytivas site i Fyrislund i Uppsala. Som sektionschef för Biacore leder du ett produktionsteam bestående av 14 operatörer och 5 ingenjörer som tillsammans ansvarar för tillverkningen av förbrukningsartiklar till våra Biacoreinstrument.
Huvudsakliga arbetsuppgifter och ansvarsområden:
Rollen som sektionschef innebär ett omväxlande arbete med arbetsmiljö-, personal- och budgetansvar för din verksamhet. Du ingår i avdelningens ledningsgrupp och leder din sektion och dess medarbetare framåt genom kontinuerliga förbättringar.
Utöver ditt ansvar för sektionens reguljära tillverkning ingår även att:
Initiera processvårdsaktiviteter.
Ansvara för ständiga förbättringar.
Driva förändringsärenden och produktivitetsförbättringar.
Ta emot och skala upp nya produkter.
Initiera och driva underhållsarbete.
Ekonomisk uppföljning samt att initiera och driva business case för nya investeringar.

De huvudsakliga kraven för tjänsten innefattar:
Högskoleutbildning inom relevant område, alternativt motsvarande arbetslivserfarenhet.
Goda kunskaper om industriell produktion- och processteknik.
Erfarenhet av att leda och utveckla team.
Du kommunicerar flytande på både svenska och engelska.

Det är meriterande om du även har:
Demonstrerad erfarenhet av att driva produktivitetshöjande förbättringsarbeten.
Goda kunskaper om ekonomisk uppföljning.
Goda kunskaper om leanprinciper.

För att vara framgångsrik i denna roll ser vi gärna att du som söker är en trygg ledare som trivs att jobba både med teknik och med människor. Det är av stor vikt att du är en säkerhets- och kvalitetsmedveten person som också har god förmåga att fatta initiativ, driva parallella aktiviteter och utveckla effektiva team.
Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. För frågor relaterade till tjänsten kontakta rekryterande chef Cecilia Wåhlin, Director - Manufacturing, [email protected]. Visa mindre

QA Specialist Quality Management System

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn idea... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
The QA Specialist - Quality Management System (QMS) will work closely with the Change Control Process Leader and the CCQA team to drive Change Control errands across the business. In addition, the QA Specialist - QMS will play a key role in supporting other QMS processes and tasks within the wider QA department.
This position reports to the Senior Section Manager - QA Projects, and is part of the Quality Assurance department, Quality and Regulatory Affairs, located in Uppsala and will be an on-site role.
What you will do:
Support the organization regarding QMS related topics.
Review and approve Change Control errands and prepare changes to the Change Control Board (CCB).
Support the Change Control Process Leader with process improvements.
Support other QMS Process Leaders with tasks within the QMS processes, such as assigning QMS trainings.
Review and approve quality events related to deviations and risk assessments.
Work closely with Change Leaders from different parts of the organization, the cross-functional team of certified Change Control QA as well as the Change Control Leader.
Represent QA in cross-functional risk assessments.
Attend Customer Audits to present QMS processes.
Support key quality activities and take on additional tasks supporting the overall performance of the team.

Who you are:
Bachelor's degree in Chemistry, Pharmacy, Engineering, or equivalent.
Prior experience from similar QA roles within the Life Science industry managing Change Control errands, deviations and other QMS related processes.
Knowledge of relevant quality standards and regulatory requirements (e.g., ISO 9001, ISO 13485, GMP).
Ability to communicate effectively in Swedish and English, both written and oral.

It would be a plus if you also possess previous experience in:
Proficient user of Microsoft Office software. Advanced skills in Excel is a plus.
Experience of risk assessments.
Familiarity with Lean, Six Sigma, or other process improvement methodologies.

To be successful in this role, we believe that you are a highly engaged and self-motived individual with excellent networking, interpersonal and communication skills. In addition, we're looking for a structured individual with the ability to work effectively both independently and with others. The ideal candidate should have a service-oriented mindset with quality focus and high integrity.
Interview and selection will happen continuously and the opening can be filled before the last day of application. For questions regarding the role please contact hiring manager Erika Lodén, Senior Section Manager - QA Projects, [email protected].
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Project Manager

Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
As Project Manager at Cytiva, you will be responsible for managing New product development and sustaining projects for chromatography and related consumables products for purification. You manage the full project life cycle, successful project delivery will include full implementation from initiation to deployment for one to two major or several minor/medium projects simultaneously.
This position is part of the R&D Project Management Office in the Resins and Technology OpCo, located in Uppsala, Sweden, and will be an on-site position. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
In this role, you will have the opportunity to:
Coordinate and execute cross-functional projects focused on the delivery of novel chromatography resins and technology products to the Bioprocessing market and support the launched products through sustaining projects.
Define and plan projects involving multiple functions and stakeholders and maintain active dialogue with business area representatives, to ensure project deliveries are aligned with developing market needs.
Ensure that projects/programs are proceeding according to scope, schedule, budget, and quality standards. Manage deviations, quality objectives, regulatory requirements, schedules and program risks and make decisions based on business objectives.
Drive the achievement of Project and Portfolio KPIs through the adoption of Danaher Business Systems tools such as Visual Project Management, Daily Management and Project Management Standard Work/Methodology.
Working in a global environment with stakeholders and project members at different sites.

The essential requirements of the job include:
MSc or BSc in Science, Engineering or Chemistry field.
Project manager training or equal experience of industrial project management from leading projects or acting as a sub-project manager in a major projects.
Several years of project management experience from technology product development or sustaining projects.
Basic knowledge in chemistry relevant to development of chromatography resins.
English and Swedish as a working language.

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Scientist Fast Trak EMEA

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
We are looking for a Fast Trak Scientist to join our Fast Trak team, a global organization within Cytiva that works to support our customers in the biopharma industry.
The Fast Trak Scientist is part of the Fast Trak EMEA team based out of Uppsala, Sweden. We are a dynamic and customer-facing team with great opportunities to develop and grow through a broad variety of process development services for various biomolecules as well as training courses supporting the EMEA biopharma industry. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
In this role, you will have the opportunity to:
Focus on chromatography techniques and you will be coordinating activities and working directly with our customers in a dynamic and collaborative environment, acting as subject matter expert.
You will take the role as an expert in discussions with the customer, develop and/or transfer methods and perform experiments during projects.
You will work proactively to contributing to process development projects with creative ideas on how to best solve challenges using already in-place solutions or proposing the implementation of new ones.
Conduct independent scientific work on customer process development projects with monoclonal antibodies, vaccines, recombinant proteins, plasmids etc., including both administrative and laboratory work, both for analytics and bioprocessing.
Deliver training courses for customers, theoretical as well as practical, in the field of biomanufacturing.
To effectively perform the job, you will develop and nurture your internal network within the local and Fast Trak global scientific teams while also securing a creative environment in the customer projects to support and identify successful and scalable solutions for their biomanufacturing processes.

The essential requirements of the job include:
MSc in biotechnology, bioprocess/biomedical engineering or related life sciences field.
Experience working with chromatographic methods (e.g., affinity chromatography, SEC, IEX).
Experience from large scale downstream processes is strongly advantageous.
Experience from analytical techniques such as PCR, electrophoresis and ELISA/SPR methods.
Strong presentation and communication skills. Since working language is English advanced English skills is required both in oral and writing.
A valid EU work permit is required for this role.
Preferably you also have industrial experience in downstream processing of biomolecules or viral vectors.

To be successful in this role, we believe that you are a person who thrives working in a flexible environment with demonstrated abilities to navigate in a collaborative, matrixed, and customer focused environment. You have a strong ability to spot customer needs, communicate solutions and build trust by collaborating to implement effective analytical methods.
Interview and selection will happen continuously, and the opening can be filled before last day of application. For questions regarding the role please contact hiring manager Jesper Hedberg at [email protected]. We look forward to hearing from you!
Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Research Engineer

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
We are looking for a Research Engineer for our team in Uppsala. You will, as part of R&D, contribute to the development of new products which are used in the manufacturing of leading biological drugs. You will also take active part in trouble shooting of existing Cytiva processes. The Uppsala Cytiva site is the workplace for more than 1500 people including in addition to R&D also functions as manufacturing, marketing, quality control and QA. Cross-functional activities in collaboration with other units will represent an important part of work responsibilities.
This position has a strong focus on hands-on synthesis work in lab scale with focus on development of chromatography resins for bioseparations. Hence the person suited for this opening should enjoy working in a chemistry lab.
What you will do:
Perform experimental work within the area of surface/polymer/organic chemistry with focus on particle generation
Work in science projects as well as product development
Perform primary characterization
Independently plan and accomplish given tasks from Project Manager or Section Manager, to reach given project objectives
Document and report results both orally and written

Who you are:
BSc. Or MSc, or equal experience in chemistry, chemical engineering or similar
1-2 years of work experience in relevant field
Documented laboratory experience
Fluency in English and Swedish, both written and oral communication
Structured and organized team player
Valid work permit

Meritorious:
Experience of work with polysaccharides
Experience from emulsification work
Experience from development of chromatography resins

Interview and selection will happen continuously, and an opening can be filled before last day of application, which is January 20th, 2025.
Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Senior QA Specialist - Quality Management System

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas ... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
We’re looking for a Senior QA Specialist – Quality Management System to join Cytiva’s Quality Assurance Department located at our manufacturing site in Uppsala. In this role, you will be responsible for independently managing documentation within the eDMS as required to support the Uppsala QMS. As Senior QA Specialist, you will coordinate the management of documents and take on the role as Site Subject Matter Expert for our eDMS, coaching individuals on how to write instructions and chair the site Document Review Board. In addition, you will support the assignment of QMS Training and the overall performance of and compliance to the Uppsala QMS together with QA Leaders. This is a highly dynamic role where you will have many cross functional interactions, both local and global. This position is an onsite role.
What you will do:
Lead and develop the Quality Management System (QMS) ensuring the effectiveness of QMS and its documentation.
Lead the QMS Documentation Review Board including multi-site documentation ensuring the QMS documentation process is effective and continuously improved by monitoring performance.
Act as Site subject matter expert (SME) for our document management system (eDMS) and in global forums.
Monitor changes in global and external documents and assure that relevant changes are initiated and managed in the site QMS document process.
Work closely with the Site QA Leader and the respective SME to understand, develop and harmonize the QMS and related documentation and training.
Support the QMS Training Lead and the Line and Quality Managers with the planning and organizing of QMS Training, ensure the training matrix is updated, track QMS Training metrics and create training material as relevant
Administrate the QA webpage on Cytiva's intranet.

The essential requirements of the job include:
Bachelor’s degree or high school diploma in a relevant field.
A few years experience of working in an documentation-focused role within a ISO9001, 13485 or cGMP regulated environment.
Ability to communicate effectively in Swedish and English, both written and oral.
Experience working with computerized systems.
Proficient user of Microsoft Office software. Advanced skills in Excel is a plus.

To be successful in this role, we believe that you are a highly engaged and self-motived individual with excellent networking, interpersonal and communication skills. In addition, we're looking for someone who is very structured, enjoys problem-solving and troubleshooting, with the ability to work effectively both independently and with others. The ideal candidate should possess a service-oriented mindset, demonstrate unwavering integrity, prioritize quality, and consistently meet deadlines.
Interview and selection will happen continuously and the opening can be filled before last day of application. For questions regarding the role please contact hiring manager Camilla Lindgren, QA Section Manager, [email protected].
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Team Lead Prototypverkstad

Bli en del av något helt livsavgörande Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier. Som del av Cytiva kommer du kontinuerligt förbättra dig själv och oss – du kommer att bidra ... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier.
Som del av Cytiva kommer du kontinuerligt förbättra dig själv och oss – du kommer att bidra till att lösa utmaningar som har verklig betydelse för människors hälsa tillsammans med kollegor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i över 40 länder är Cytiva en arbetsplats där varje dag är en möjlighet att lära sig mer – så att du kan fortsätta utvecklas i din karriär och stärka dina färdigheter över tid.
Vi är en del av Danahers bioteknologisegment och sammanför teknisk expertis och talang från hela världen för att utveckla nästa generations livsförändrande terapier.
Prototypverkstaden på RnD består idag av 7 erfarna medarbetare. Vi arbetar med CNC-styrda 3- och 5 axliga fräsar, svarvar, vattenskärningsutrustning och lasersvetsar såväl som med manuella maskiner och det senaste inom mätteknik för uppmätning av detaljer. Vi tillverkar prototypdelar till nästa genarations produkter för forskning och storskalig tillverkning av läkemedel och vacciner. Vi gör även utrustning som används internt på våra labb och viss utrustning som används i vår interna produktion. Vi samarbetar mycket nära vårt Center of Exellence för additiv tillverkning.
Vi söker en ingenjör med inriktning mot mekanik som ska vara samanhållande för det dagliga arbetet och drivande i den fortsatta utvecklingen med planering/uppföljning samt vara delaktig i investering av ny utrustning. Du kommer även att vara husansvarig för två st RnD-byggnader och den som driver frågor relaterat till arbetsmiljö och säkerhet inom verkstadens lokaler. Är du intresserad av att vara med och utveckla vår verksamhet? Då vill vi höra ifrån dig.
I den här rollen kommer du få möjligheten att:
Leda och koordinera arbetet i prototypverkstaden.
Ansvara för att prototypdelar tas fram enligt utvecklingsprojektens krav och tidsplaner och ansvara för prioritering.
Själv tillverka prototypdetaljer för att bidra till verkstadens leveransförmåga.
Säkerställa att verkstaden upprätthåller hög standard vad gäller säkerhet och kvalitet.
Samarbeta med utvecklingsteam för att optimera prototyptillverkningen och se till så att teknisk expertis och förmågor i prototypverkstaden används på bästa sätt.
Utveckla och implementera förbättringar i arbetsflöden och processer inom verkstaden.
Driva investering i ny teknologi och ny utrustning i samarbete med övriga verksamheter.
Driva frågor relaterat till husansvar som att vara med och kravställa ombyggnationer och planera in löpande underhåll.

De huvudsakliga kraven för tjänsten är:
Högskoleingenjör eller motsvarande kompetens med 10 års relevant arbetslivserfarenhet.
Kunskap och erfarenhet från tillverkning i CNC-styrda maskiner.
Erfarenhet som teamledare.
Erfarenhet från att jobba med frågor som arbetsmiljö och säkerhet.
Stort eget driv och tekniskt intresse med en vilja att utveckla teamets förmågor.
Flytande i svenska och engelska, såväl tal som skrift.

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Produktionsingenjör

Bli en del av något helt livsavgörande Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier. Som del av Cytiva kommer du kontinuerligt förbättra dig själv och oss – du kommer att bidra ... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier.
Som del av Cytiva kommer du kontinuerligt förbättra dig själv och oss – du kommer att bidra till att lösa utmaningar som har verklig betydelse för människors hälsa tillsammans med kollegor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i över 40 länder är Cytiva en arbetsplats där varje dag är en möjlighet att lära sig mer – så att du kan fortsätta utvecklas i din karriär och stärka dina färdigheter över tid.
Vi är en del av Danahers bioteknologisegment och sammanför teknisk expertis och talang från hela världen för att utveckla nästa generations livsförändrande terapier.
Vi söker en Produktionsingenjör till sektionen Renrumsproduktion. Vi är en del av den kemiska produktionen på Cytivas fabrik i Uppsala. Gruppen som vi söker Produktionsingenjör till arbetar med att tillverka “Ready to Process” kromatografikolonner. Produktionen sker i ISO-klassat renrum.
Att arbeta som Produktionsingenjör hos Cytiva betyder framför allt att du är ett dagligt stöd till produktionen. Rent praktiskt kan det innebära att du arbetar med att:
Daglig uppföljning av produktionen.
Driva Change Control-ärenden och avvikelsehantering.
Teknisk felsökning av processutrustning.
Kontakt med underhållsavdelning och/eller entreprenörer.
Samarbeta med F&U vid nyproduktprojekt och produktvårdsprojekt.
Agera som stöd i reklamationsärenden och driva utredningar rörade reklamationer.

Du driver även förbättringsarbete, uppdaterar produktionsdokument samt utför och dokumenterar riskanalyser mm. Ingenjörsarbetet präglas av variation och en möjlighet till att påverka den dagliga verksamheten, där tillverkningen står i fokus.
De huvudsakliga kraven för tjänsten är:
Högskoleingenjör eller motsvarande med inriktning mot bioteknik/kemiteknik/maskinteknik eller liknande utbildningsbakgrund.
Du behärskar svenska och engelska flytande i tal och skrift.
God datorvana och trygg användare av olika IT-system.

Det är även meriterande om du har tidigare erfarenhet av:
GxP kunskap
Erfarenhet av kolonnpackning
Erfarenhet av processindustri/läkemedelsindustri

För att vara framgångsrik i denna roll ser vi gärna att du är en lagspelare med god samarbetsförmåga och att du trivs i med att jobba både med teknik och med människor. Vidare ser vi gärna att du är en säkerhets- och kvalitetsmedveten person med god förmåga att ta initiativ och driva flera parallella aktiviteter samtidigt.
Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Validation and verification engineer

Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The Validation and Verification Engineer is responsible for performing verification on time with guidance from senior engineers, planners and project managers according to customer demand.
The Verification section is responsible for planning and execution of functional tests on Bioprocess equipment developed by Custom Engineering.
This position is part of the Verification section in Uppsala and will be an on-site role. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
In this role, you will have the opportunity to:
Verification:
Functional testing of Custom engineering equipment.
Support projects to ensure quality and timely delivery of plans and results through daily management.
Support planning and development activities for coming projects.
Participate in customer FATs.
Participate in troubleshooting and suggestion of corrective actions for products, test methods, procedures etc.
Quality inspections of products at sub supplier or at Custom engineering.

Documentation:
Deliver verification documentation and test results.
Participate and or propose development of wow/procedures/methods.

Service/Expertise:
Support training of new resources, secure that GDP and other regulatory requirements are understood and fulfilled.
Support maintenance & development of test facility and test equipment.
Perform installations/troubleshooting at customer site.
Support service with maintenance and repair of customized equipment.
Participate in resolution of case management, CAPA, risk analysis.

The essential requirements of the job include:
Bsc. in mechanical or electrical engineering or similar knowledge from working experience.
GMP knowledge or experience from other regulated business areas.
Experience from testing/verification of operating systems.
Knowledge from Cytiva Bioprocess products.
Fluency in English, both written and spoken.

It would be a plus if you also possess previous experience in:
Fluency in Swedish. Visa mindre

Additive Design Engineer

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas ... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
We are looking for an Additive Design Engineer to join our dynamic Additive Manufacturing (AM) team, which is part of our global Central Technology Organization. The team is responsible for driving the scientific and technology agenda within the AM field, providing support and expertise to new product development and R&D teams across Cytiva. This position is an onsite role, based at our site in Uppsala, Sweden, and is a temporary position (until March 2026).
What you will do:
Drive Design for Additive, and support build-up of capability in the global Cytiva organization. Engage in training of design engineers and manufacturing engineers.
Contribute with expertise on CAD design and adjacent technical solutions.
Work closely with R&D teams in all Cytiva business units: independently lead, perform, and support design for additive activities in projects – from idea and concept development, via prototyping, to transfer to production.
Evaluate and implement new additive technologies and materials, both polymer and metal.
Provide hands-on support in 3D printing and post-processing work – to understand how design and production processes are interconnected, and how both can be improved.

The essential requirements of the job include:
BSc or MSc in Mechanical Engineering, or equivalent educational background.
A few years experience working with mechanical design.
Strong working knowledge of CAD software (e.g. Creo, SolidWorks) and file management.
Experience of additive manufacturing (3D printing), alternatively experience of CNC machining and/or injection molding.
Fluency in English – both written and verbal.

It would be a plus if you also possess previous experience in:
Proven ability to lead small technical projects.
Fluency in Swedish – both written and verbal.

To be successful in this role, the ideal candidate should be an excellent communicator with strong interpersonal skills, possess a creative mindset, focus on customer needs, excel in cross-functional collaboration.
Interview and selection will happen continuously, and the opening can be filled before last day of application, January 3rd, 2025. For questions regarding the role please contact hiring manager Bo Medhage, Director - Additive Manufacturing, [email protected]. Welcome with your application! Visa mindre

Senior HR Business Partner

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn idea... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
What you'll do:
As Senior HR Business Partner at Cytiva, you will be responsible for the short and long-term strategic leadership of all aspects of HR management for the assigned client groups within BioProcess. You will serve as an advisor and counsel to global leadership teams to help them achieve their business goals through effective HR strategy deployment and by providing guidance as needed for effective decision making.
The incumbent will also be responsible for providing leadership and direction to the global and local Human Resource teams supporting the assigned client groups within BioProcess in the acquisition and development of talent as well as creating and maintaining a highly productive and engaging work environment. You will serve as a thought leader and partner in advancing organizational capabilities and effectiveness and will provide lead organizational and talent development efforts to meet strategic and annual business objectives.
Additionally, the Senior HR Business Partner will also focus on developing a culture that facilitates open communication with leadership, advances the Associate value proposition and educates associates on how they contribute to enterprise-wide goals. Key responsibilities include, but are not limited to:
Proactively engage with the leadership team for assigned client groups, acting as a thought partner on business, people and organization-related opportunities to drive business results and build culture.
Determine organizational implications of business strategy; facilitate organizational diagnosis and metrics to drive organizational effectiveness through talent and organizational capabilities and culture.
Partner with local HR and Talent Management to drive annual strategic talent processes.
Assess and identify talent acquisition needs; partner with local HR and Talent Acquisition teams to build talent pools, cultivate talent, identify critical capabilities, etc.
Enable leaders to assess and create talent development opportunities and facilitate cross-functional talent movement.
Assess and identify retention and engagement trends; partner with local HR and Talent Management teams to develop and implement retention and engagement strategies.
Act as an advisor to leaders during times of change and partner with the business to develop and implement change management and communication plans.
Provide coaching and guidance for performance improvement, facilitating difficult feedback and other employee relations support for leaders of assigned client groups. Partner with regional HR teams to identify performance management trends in the organization and identify countermeasures to close gaps.
Act a consultant and advisor on Diversity, Equity & Inclusion to further learning and capability.
Through DBS, identify key targets to improve/metrics to analyze and solve business problems that impact organizational effectiveness. Lead cross OpCo / BU / Regional improvement projects as assigned.
Partner closely with the HR Centers of Excellence (COEs) and Regional HR teams to execute programs, processes and practices, including Performance Management, Retention and Engagement efforts, Learning and Development, Compensation Planning, and Organization Talent Review.

Who you are:
We are looking for a consultative Human Resources professional who is experienced with providing a variety of HR solutions to meet business needs. You love analyzing data, identifying continuous improvement opportunities, and excel in building relationships with business stakeholders in a matrixed, collaborative and an environment.
A Bachelor’s degree in Industrial/Organizational Psychology, Human Resource Management, Business Administration, or a related field.
8+ years of experience in progressive roles in human resources, with prior experience leading a global team.
Demonstrated experience as a cross-functional partner who collaborates well and can indirectly influence in a matrixed environment.
A self-motivated individual who is comfortable operating with minimal direction and who thrives in a dynamic environment as a leader influencing change and transformation.
Credible and savvy business partner who will be perceived as a trusted consultant and functional expert to senior management.
Mission-driven individual with high energy and strong levels of perseverance; works toward both individual and team goals.
Developer of cross-functional HR talent; Committed to elevating the overall HR function.
Demonstrated critical thinking and problem-solving capabilities, and possesses intellectual curiosity, agility, and resourcefulness.
Capable of rolling up one’s sleeves to do what it takes to drive results; not hindered by process or ambiguity.
Willing to travel approximately 20% of the time.

Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
Interview and selection will happen continuously, and the opening can be filled before last day of application. For questions regarding the role please contact hiring manager Susanne Spang, Senior HR Director, at [email protected]. We look forward to reading your application! Visa mindre

HR Generalist

Ansök    Nov 28    Cytiva Sweden AB    HR-chef
Bli en del av något helt livsavgörande Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier. På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att ar... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier.

På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbeta med utmaningar som verkligen spelar roll tillsammans med människor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i 40 länder är Cytiva en plats där varje dag är en möjlighet att lära så att du kan få fart på din karriär och förbättra dina färdigheter på lång sikt.
Vi på Cytiva är stolta över att arbeta tillsammans med en grupp av nio andra Danaher Life Sciences-företag. Tillsammans är vi pionjärer inom vetenskap och medicin och utvecklar produkter som hjälper forskare i kampen att rädda liv.

Vi söker nu en HR Generalist till vårt HR team i Uppsala. Vi letar efter dig som har en personlig mognad, högt driv och ett välorganiserat arbetssätt. Du har en god kommunikationsförmåga och har lätt för att skapa och bibehålla goda relationer. Du är professionell, har ett positivt förhållningssätt och fungerar som en "go-to person" för HR-teamet och de chefer som teamet stödjer.

Denna roll kräver särskild uppmärksamhet på dataintegritet och analys för att stödja avgörande HR beslut och processer. Du kommer att arbeta tvärfunktionellt med interna team och bidra aktivt till HR-teamets framgångar.
Arbetsuppgifter:
Stödja HR-teamet i deras dagliga arbete
Första linjens HR-support
Hantering av HR systemet Workday och Service now
Bibehålla och skydda konfidentiella data med största noggrannhet, omdöme och omsorg
Assistera och driva HR-projekt, evenemang eller initiativ vid behov
Hantera on/offboardingprocessen
Hantering av fackliga dokument
Planera, samordna och genomföra program för nyanställda samt introduktionsprogram för nya chefer


Vem är du:
Detaljorienterad med stark genomförandeförmåga
Förmåga att förutse och lösa utmaningar
Hög energinivå med stort kundfokus
Utmärkt kommunikationsförmåga
Flytande i svenska och engelska, både i tal och skrift


Du behöver:
Högskoleexamen inom HR, eller annan högskoleutbildning/erfarenhet som bedöms likvärdig
God system- och datorvana, inklusive kunskaper i Excel
Mycket god kommunikationsförmåga


Meriterande:
Erfarenhet av Workday och ServiceNow



Urval och intervjuer sker löpande så vänta inte med dig ansökan.
Vi ser fram emot din ansökan.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Finance and Reporting Analyst

Ansök    Nov 28    Cytiva Sweden AB    Finansiell controller
Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
We are looking for a Finance and Reporting Analyst, RFM to support analytics, forecasting and reporting to RFM (Resin, Filtration, and Cell Culture Media) Finance leaders and CFO.
The individual, as a member of the RFM Finance team, will play a key role in the continuous improvement of our financial processes and is expected to embrace contemporary digital finance capabilities. The role is located in Uppsala, Sweden and will be on-site role.
What you will do:
Lead reporting responsibilities for RFM (Resin, Filtration, and Cell Culture Media) organization including monthly and weekly performance metrics (Bowler), actuals and Forecast summary (Flash Color), and support providing key data for the business summary (President letter).
Lead consolidation of Commercial performance and analyze the data to provide timely business insight for the senior RFM leadership team
Owns forecast and closing process for RFM cost by coordinating with multiple business unit stakeholders and drive cost out initiatives to enhance productivity
Support Business Unit and FP&A Finance leaders by developing and updating operational review templates
Support and own monthly forecasting processes across RFM business units and consolidation of the annual budget; act as a challenge function to business unit finance leads when consolidating and pacing financial performance
Act as the key RFM lead for broader Finance initiatives such as Kaizen, SOX, and IT-Finance and reporting enhancements


Who you are:
Bachelor’s degree in Accounting, Finance, or Business Administration
Minimum of five years of financial work experience, including developing forecasts & operating plans and leading business / finance reviews.
Drivers, generate alternatives and drive positive change
Clear thinking/problem solving: successfully led cross-functional projects/process improvement within operations/finance function; able to quickly grasp new ideas
Solid PC skills: experience with financial systems/applications (i.e.: Oracle, SAP, OneStream, Qlik or other BI tool, etc.), strong Excel skills in data compilation and aggregation (i.e. pivot tables, VLookup, and Macros)

Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. Visa mindre

Section Manager R&D

Ansök    Dec 3    Cytiva Sweden AB    Manager
Be part of something altogether life-changing! Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that trul... Visa mer
Be part of something altogether life-changing!
Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives
We are looking for a Section manager for the Affinity Ligand Design team within the Resin & Ligand Design Department in Resin & Technologies R&D. This section is placed in Stockholm, Solna at Karolinska. The section is responsible for designing new protein affinity ligands and for developing and continuously improving the tools needed for designing these new ligands.


What You'll Do
You will supply Research and Idea evaluation ligand related projects with resources according to the needs in term of time and competences, and secure that deliveries from the section are executed in an efficient and timely manner, and with appropriate quality according to agreed standards.
You will secure that the competence and know-how of the section members is appropriate to support the organization in the field the section is responsible for, and that competences are continuously developed via education, seminars, coaching, mentoring and individual developmental plans.
You will drive the development of the section to improve productivity, establish processes and a strategy to secure long term technology development within the section’s responsibility areas.
You will work in partnership with other Section managers, Project and Program managers and Product management, Marketing and other critical functions.
You will be accountable for the working environment within your team.



Who you are
A strong people leader and experienced in Life Science product development that can balance resources, timing and quality of outcomes.
You have a PhD in biotechnology, biochemistry or related Life Science field or equivalent knowledge or experience.
At least 5 years of experience of industrial development/R&D in the Life Science area
Track record of successful cross-functional collaborations
We are looking for someone with a good ability to motivate, direct and develop people
In order to succeed in this position you need to be motivated, result-oriented, flexible and creative with a strong collaborative attitude, focusing on the customer needs
Live in the area nearby Stockholm and have the possibility to commute to our sites in Solna and Uppsala



Application
We continuously assess candidates and invite them for interviews, so please don’t hesitate to write and send in the application. The recruitment will be completed as soon as a suitable candidate is found. We look forward to seeing your application. Visa mindre

Column Engineer - Temp

Bli en del av något helt livsavgörande Är du redo att accelerera din potential och göra verklig skillnad inom biovetenskap, diagnostik och bioteknik? På Cytiva, ett av Danahers 15+ operativa företag, räddar vårt arbete liv – och vi är alla förenade av ett gemensamt engagemang för att förnya för påtaglig effekt. Du kommer att trivas i en samhörighetskultur där du och din unika syn är viktig. Och genom att utnyttja Danahers system för ständiga förbättringar ... Visa mer
Bli en del av något helt livsavgörande
Är du redo att accelerera din potential och göra verklig skillnad inom biovetenskap, diagnostik och bioteknik?
På Cytiva, ett av Danahers 15+ operativa företag, räddar vårt arbete liv – och vi är alla förenade av ett gemensamt engagemang för att förnya för påtaglig effekt. Du kommer att trivas i en samhörighetskultur där du och din unika syn är viktig. Och genom att utnyttja Danahers system för ständiga förbättringar hjälper du till att omvandla idéer till genomslag – innovativa i livets hastighet.
Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier.
På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbeta med utmaningar som verkligen spelar roll tillsammans med människor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i 40 länder är Cytiva en plats där varje dag är en möjlighet att lära så att du kan få fart på din karriär och förbättra dina färdigheter på lång sikt.
Vi på Cytiva är stolta över att arbeta tillsammans med en grupp av nio andra Danaher Life Sciences-företag. Tillsammans är vi pionjärer inom vetenskap och medicin och utvecklar produkter som hjälper forskare i kampen att rädda liv.
Vi söker en Column Engineer som vill jobba med att producera kundanpassade kromatografikolonner.
Den här tjänsten rapporterar till Sr Manager, CDP och är på plats i Uppsala, Sverige. Detta är en tidsbegränsad anställning med start 16 December 2024 till 31 December 2025 eller enligt övernskommelse.
Dina arbetsuppgifter
Som en del i ett team av fyra kollegor kommer du bidra till framtagningen av mestadels kundanpassade kolonner, men även andra typer av labbprodukter - vilka används vid framtagning av läkemedel som till exempel vacciner och cancerläkemedel.
Du kommer ansvara för att, på labb, producera leveranser av kundspecifika produkter och se till att en del av sortimentet finns på lager. Arbetet innefattar också att tillsammans med övriga sektionsmedlemmar planera och strukturera processen, svara på kundfrågor och agera på offerter samt registrering och uppsättning av nya produkter inklusive batchprotokoll, certifikat, och skeppningsdokument.
Du kommer få en bra översikt av stora delar av företaget och arbeta med uppgifter inom produktutveckling och produktion. Som teammedlem i CDP har du kontakt med interna instanser som: Product Management, R&D och även säljorganisationen, vilket gör att du får insyn i kundbehoven och kundens vardag.
Vem är du
Ingenjörsexamen, utbildning som arbetsgivaren bedömer likvärdig eller relevant arbetslivserfarenhet som motsvarar
Minst fem års arbetslivserfarenhet av labarbete, metodutveckling, produktion eller kvalitetssäkring inom Life Science-området
Erfarenhet av Oracle och/eller Magic eller kolonnpackning är meriterande
Du behärskar svenska och engelska obehindrat både i tal och i skrift
Förmåga att arbeta både självständigt och i team
EU arbetstillstånd är ett krav

Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas. Varmt välkommen med din ansökan! Visa mindre

Underhållsingenjör

Ansök    Nov 26    Cytiva Sweden AB    Underhållsmekaniker
Bli en del av något helt livsavgörande Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier. På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbe... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier.
På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbeta med utmaningar som verkligen spelar roll tillsammans med människor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i 40 länder är Cytiva en plats där varje dag är en möjlighet att lära så att du kan få fart på din karriär och förbättra dina färdigheter på lång sikt.
Vi på Cytiva är stolta över att arbeta tillsammans med en grupp av nio andra Danaher Life Sciences-företag. Tillsammans är vi pionjärer inom vetenskap och medicin och utvecklar produkter som hjälper forskare i kampen att rädda liv.
Sektionen Maintenance söker en underhållsingenjör som är en del av kemisk produktion inom Cytiva i Uppsala. Vår sektion består av 28 personer som arbetar med fortlöpande tillsyn, underhåll och utveckling av processutrustning. Tjänsterna inom sektionen består av styr- och reglertekniker, underhållsmekaniker, serviceingenjör, underhållsingenjör och underhållsspecialister. Tjänsten är en tillsvidareanställning.
Vad du ska göra
Statistikuppföljning inom Underhåll
Support till produktion vad gäller teknikval samt planera in byten eller service
Stöd till Projektavdelningen vad gäller sitestandard, Basic design.
Kartläggning av sitensprocessutrustning av gäller ålder, BAT, kapacitet
Planering av servicedagar

Vem du är
Minst gymnasieingenjör inom maskin, el- eller datorteknikutbildning samt flerårig yrkesvana
Brett tekniskt intresse
Serviceinriktad
Förändringsbenägen och drivande
Strukturerad och noggrann
Förmåga att samarbete i grupper
Administration av underhållsarbete
Erfarenhet av datoriserade underhållsprogram
Kan tala/skriva svenska och engelska.
Skall jobba från vår site i Uppsala på daglig basis.

För frågor kring tjänsten vänligen kontakta anställandechef Martin Frick på [email protected]. Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. Varmt välkommen med din ansökan! Visa mindre

Research Engineer, Bioprocess R&D

Be part of something altogether life-changing Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly... Visa mer
Be part of something altogether life-changing
Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.
Cytiva is looking for a Research Engineer Bioprocess R&D for on-site position in Uppsala
What you’ll do
Be part of a team of scientist that develop, invent and improve new products and processes for the bioprocess industry.
In collaboration with the team, plan, perform, analyze, document and present mammalian cell culture experiments in different formats, with a focus on suspension cells.
Independently solve problems of "trouble shooting character" in project work.
Maintain laboratory notebooks in accordance with company policy and legal requirements.
Plan and carry out committed tasks against agreed objectives.
Present scientific and technical results internally, through oral and written communication.

Who you are
To succeed in this position, you need to be a team-player, open-minded, result-oriented, flexible and creative with a strong collaborative attitude, focusing on the customer needs.
We are looking for someone with the drive and capability to initiate, in collaboration with others, plan, perform, analyze, document and present results to progress our projects forward.
Master´s degree in biology, engineering, or related Life Science field.
Practical experience in handling of mammalian cell culturing in different formats.
Hands on experience in analytical and cell culture techniques.
Occasional work on weekends will occur.

Application
We continuously assess candidates and invite them for interviews, so please don’t hesitate to write and send in the application. The recruitment will be completed as soon as a suitable candidate is found.
We look forward to seeing your application.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Global Repair, Parts & Tools Engineer

Bli en del av något helt livsavgörande Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier. Som del av Cytiva kommer du kontinuerligt förbättra dig själv och oss – du kommer att bidra ... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier.
Som del av Cytiva kommer du kontinuerligt förbättra dig själv och oss – du kommer att bidra till att lösa utmaningar som har verklig betydelse för människors hälsa tillsammans med kollegor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i över 40 länder är Cytiva en arbetsplats där varje dag är en möjlighet att lära sig mer – så att du kan fortsätta utvecklas i din karriär och stärka dina färdigheter över tid.
Vi är en del av Danahers bioteknologisegment och sammanför teknisk expertis och talang från hela världen för att utveckla nästa generations livsförändrande terapier.
Vi söker nu två personer till rollen som Remanufacturing/Repair Shop Engineer till gruppen Global Service Center på Cytivas site i Umeå. Vi är ett team på 9 personer som arbetar med renovering av hela instrument och dess reservdelar. I arbetet med renovering ingår felsökning, demontering, montering samt test. Utöver detta arbetar gruppen med att bistå Cytivas fältingenjörer med kalibrering av verktyg, kontroll av reservdelar och även utföra service av hela instrument. Tjänsten är helt on site.
I den här rollen kommer du få möjligheten att:
Felsöka, renovera och testa reservdelar till Cytivas instrument.
Arbeta tillsammans med dina kollegor för att lösa produktions- och kvalitetsproblem relaterade till test och renovering.
Kvalitetskontroll och paketering av reservdelar.
Vara delaktig i den dagliga planeringen inom gruppen, hålla ordning och reda, utveckla arbetsmetoder samt följa gällande lagar, regler och policys.

De huvudsakliga kraven för tjänsten är:
3-årig gymnasial utbildning inom teknik eller minst 2 års erfarenhet av montering inom tillverkningsindustri.
Lagspelare, med god samarbetsförmåga och van av att jobba både med teknik och människor.
Goda kunskaper i svenska och engelska, såväl muntligt som skriftligt.

Det är även meriterande om du har tidigare erfarenhet av:
ÄKTA Avant /Pure och dess reservdelar.
Att arbeta i Magic och Oracle. Visa mindre

Senior Manager - QA Custom Hardware

Ansök    Nov 19    Cytiva Sweden AB    Kvalitetschef
Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The Senior Manager QA for Custom Engineering & SCO (Standard and Custom Operations) Sweden, independently leads, coordinates and prioritizes the work within the assigned site/s to ensure successful management of the QMS and associates processes.
The role is responsible for ensuring that the Custom Engineering Sweden team executes on deliveries, internal audits, QMS training, QMS documentation, complaints, NC/CAPA, product holds and field actions. Ensures compliance of the processes and drives a strong Quality Culture by engagement, empowerment, and inclusiveness.
This position is part of the QA Custom Hardware department located in Uppsala, Sweden and will be onsite. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
What you will do:
Be responsible for engaging strong intra departmental and cross-functional/organizational relationships to drive compliance and ensuring product quality.
Be the QA representative in project steering committees as agreed with QA Director.
Lead, coordinate, prioritize and follow-up the work within the team.
Engage, coach and develop the personnel.
Set goals for the team and follow up on completion.
Drive internal improvement work to assure continuous improvements.
Support key quality activities and be open to take on additional tasks supporting the overall performance of the QA Department.

Who you are:
Bachelor’s degree preferably in a science or engineering discipline.
A minimum of 5 years of experience in the Quality Assurance field.
Experience of working as a manager within Quality Assurance/Quality Control
Comprehensive understanding of ISO 9001 requirements.
Experienced in continuous improvement methodologies & tools.
Experienced in leading external audits, including customer communications.
Excellent organizational, presentation, meeting facilitation and technical writing skills.

It would be a plus if you also possess previous experience in:
Knowledge and awareness of the methods and techniques of Quality Control in the manufacturing industry.
Technical knowledge of systems/devices used in the biopharma field.
Fluency in Swedish both written and verbal communication. Visa mindre

Delivery Fulfillment Leader

Ansök    Nov 19    Cytiva Sweden AB    Logistikingenjör
Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
We are looking for a Delivery Fulfillment Leader to join our EMEA Logistics & Fulfillment team at Cytiva's site in Uppsala, Sweden.
As a Delivery Fulfillment Leader at Cytiva, you will work closely with internal and external stakeholders to ensure delivery of goods to our customers globally - on both a tactical and strategical level.
Are you a passionate Supply Chain expert looking for an exciting opportunity within a growing business? Then we'd love to hear from you.
At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
In this role, you will have the opportunity to:
Lead the effort to ensure a comprehensive approach to identify, manage, monitor, and control fulfilment risks.
Participate and lead process improvements and initiatives in overall order management process by recommending and implementing specific improvements to work processes based on feedback collected from different internal and external partners.
Deep-dive and root cause deviations in warehouse and logistics processes impacting on time fulfilment and drive corrective actions.
Monitor deviations in warehouse processes and quality issues impacting on time fulfilment and drive corrective actions.
Coach applicable teams on root cause resolution to eliminate repeat issues.
Be the regional distribution focal point and develop a close collaboration with customer service, sales & service organizations.
Lead operating mechanisms with logistics operations and customer service teams for order execution and managing escalations.
Review Ship dates and past due Ship dates with relevant stakeholders for customer order fulfillment.
Report out on business & fulfilment reviews and drive solutions for the distribution of products.
Lead improvements for on-time delivery performance for end customer for assigned region/business unit.

The essential requirements of the job include:
Bachelor degree with project management experience.
Several years in Operational environment of Order fulfillment and Logistics Management.
Experience of improvement work using LEAN.
Proven ability to execute, multi-task, and deliver on commitments.
Solid communications and analytical skills.
Effective problem solving, root cause analytical skills.

It would be a plus if you also possess previous experience in:
ERP-systems (i.e.: Oracle, SAP or similar)
BI-tools (i.e.: QLIK, Power-BI)

Selection and interviews will be conducted continuously. Visa mindre

Customer Complaints Coordinator

Ansök    Nov 13    Cytiva Sweden AB    Kvalitetskoordinator
Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The Customer Advocacy Coordinator for Cytiva is responsible for ensuring CBS (Custom BioProcess Solutions) related customer complaints and questions are handled in an appropriate and timely manner. The team works proactively with appropriate actions to prevent similar complaints to occur.
This position is part of the Custom Engineering department located in Uppsala and will be an on-site role. Custom engineering (CE) is a department within Cytiva, developing and delivering customized hard- and software for Biopharma-industry. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
You are part of Custom engineering (CE) Life cycle management team working with customer support and quality related tasks such as complaints and questions from our global market. As coordinator you are responsible for driving quality improvements, leading CAPA investigations and implementation, you act as field modification coordinator and analyze and report quality related trends together with the team.
You will have dedicated support from SME’s (Subject matter experts) for technical details, investigations and responses.
In this role, you will have the opportunity to:
Continuously monitor cases in SFDC, allocate them to experts, and send reminders to close cases in a timely manner.
Data management of quality related statistics and present output to management and QA.
Review of quality related data gathered from SFDC, Veeva, and Magic. Assemble monthly report out.
Support implementation of Customer Defect Tracking and Resolution (CDT&R) funnel at CBS.
Ownership of Lessons Learned Smartsheet. Provide feedback to section managers. Training with team members of each section.

The essential requirements of the job include:
BSc or MSc in Biotechnology or Life Sciences.
Knowledge of Cytiva Bioprocess products to the Biopharma industry.
Experience of complaint handling, CAPA processes or similar.
Demonstrated understanding of cross-functional needs and interdependencies to successfully deliver a superior customer experience.
Excellent communication and collaboration skills.
Fluency in Swedish and English both written & oral communication. Visa mindre

Bioproces Development Scientist

Ansök    Nov 18    Cytiva Sweden AB    Biomedicinare
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas ... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible.
The Bioprocess Development Scientist is responsible for evaluating and optimizing Cytiva filtration technology in biopharmaceutical processes. The BDS advises customers on process options, runs filterability studies, and helps overcome filtration challenges in drug process development. This position is located remotely in Uppsala, Sweden and covers projects in the Nordics and Baltics territory. This position reports to the EMEA Filtration BPS Leader and is part of the BioPharma Process team and will be fully remote.


What you will do:
Engage in technical consultations with customers on downstream filtration processing where you evaluate and propose options for process optimization
Coordinate, perform and analyze bench scale test work at customer site for Cytiva filtration technologies in customer’s biopharmaceutical processes.
Serve as a technical specialist with in-depth knowledge of Cytiva products and downstream processing and develop expertise by regular exchange of experiences and trainings.
Join a dynamic cross-functional and cross-regional team of bioprocess scientists
Work in close relationship with sales specialists, account managers, and scientists to coordinate activities and win sales
Be part of the bringing future biopharmaceuticals to patients by supporting process development of molecules such as monoclonal antibodies, recombinant proteins or vaccines



Who you are:
Master’s Degree in Life Science, Chemical or Biological, or Engineering or related field required, PhD preferred
5 plus years of relevant experience in biotech industry, preferably in downstream process development
Valid driver’s license
Willing to travel regionally (approximately 50%) with occasional travel outside assigned territory
English fluency required, Swedish language a plus Visa mindre

Technical Writer

Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The Technical Writer at Cytiva is responsible for the creation of customer-focused end-user documentation in a manner that meets corporate standards and style.
This position is part of the Technical Documentation group (TechDoc) located in Uppsala and will be an on-site role. The group produces and maintains customer-facing end-user documentation that supports products manufactured in multiple locations of Cytiva.
In this role, you will have the opportunity to:
Research, write, edit, review, proof-read, and publish end-user documentation to ensure completeness, accuracy, validity, and clarity of information for digital and/or print production in line with corporate standards for style and quality.
Work with Product Management, R&D and regulatory affairs to ensure the timely and cost-effective production of new documents and maintenance of existing documents.
Fulfil end-user documentation assignments such as production of new user documentation for new product development (NPD) or updates of existing user documentation.
Estimate and schedule the time required to complete assignments and provide regular updates of progress.
Setting up and maintaining product documentation in the Product Life Cycle Management system for traceability and design transfer.

The essential requirements of the job include:
MSc degree preferably in biology chemistry, molecular biology, or related field.
Proven experience in writing and editing technical documentation (e.g., user manuals) in a life science or medical device setting.
Proficient in English, with excellent written and verbal communication skills.
Experience of SDL Tridion or other XML based Content Management Systems.
Experience in desktop publishing tools for example Adobe InDesign, Photoshop and Illustrator.

It would be a plus if you also possess previous experience in:
Cytiva product knowledge.
CAD related tools. Visa mindre

Government Affairs Director, Sustainability

Be part of something life-changing! Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. Cytiva has played a critical role in the world’s response to the Covid-19 pandemic. We have worked closely with... Visa mer
Be part of something life-changing!
Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
Cytiva has played a critical role in the world’s response to the Covid-19 pandemic. We have worked closely with governments across the world during this period. This role will support the crucial work of helping governments prepare for future pandemics and the exciting developments in life sciences that are coming down the road.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, their patients, and governments. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.
Title: Government Affairs and Projects - Sustainability Lead
Location: Remote
Employment type: Temporary
What you'll do:
This is a global role. You will be responsible for the identification, tracking, and (where appropriate) public affairs responses to government initiatives on sustainability, the environment, and chemicals policies that impact our business and our customers. This will include, stakeholder mapping and engagement, development of the company’s position on policy issues, responding to consultation responses, advising the business policy developments,
This role is partially a project management role, ensuring that government-initiated sustainability and environmental policies are understood by the business, and that the business is responding – either by government affairs activities or by changing practices within the business.
You will need to understand the detail of the possible impact impact of government initiatives and how this may impact how the company operates and on the products it produces.
You will work closely with our existing sustainability team to ensure they are informed of forthcoming initiatives to gain their insight on how the business can respond and any issues that governments should be informed about.
You will work with colleagues to put in place plans to respond to these government initiatives. Some plans will be conducted separately by colleagues, for example, plans that necessitate the changes to products, and some will be conducted by you, for example, putting in place engagement efforts to inform policy development that will impact the company.
You will ensure compliance with the company’s government affairs policies and all relevant local transparency and engagement policies.
You will understand and infuse the highly successful Danaher Business System into your work and collaborate across multiple DHR Operating Companies, outside of Cytiva.

Who you are:
Long standing experience working in a government affairs related role, ideally with strong project management experience within a process driven and regulated industry. Life sciences experience is important.
Knowledge of sustainability and either environment and/or chemicals issues. This is widely defined and not restricted to carbon emissions. It will also consider evolving packaging, plastics, waste and/or chemicals use restrictions and policies regarding corporate due diligence.
Experience of implementing organisational projects involving multiple internal stakeholders and disciplines, across multiple jurisdictions. For external stakeholders you will have experience working with governments, think tanks, politicians and their advisers, trade organisations, and other relevant stakeholders who inform the government policy making process.

It would be a plus if you can demonstrate:
Analytical skills: the ability to digest significant volumes of data from multiple sources and draw conclusions / summarize thematically.
Confident communication skills: experience of working across multiple levels (including executive level), functions and regions; able to clearly communicate complex topics in an easy-to-understand manner; able to deliver messages effectively verbally and in writing; strong influencing skills across business functions; confidence to approach business leaders with challenges.
Adaptable/flexible: being open to change (positive or negative) in response to new information, different or unexpected circumstances, and/or to work in ambiguous situations.

At Cytiva we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Consumable Sales Specialist

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas ... Visa mer
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
The Consumable Sales Specialist for Cytiva is responsible managing and growing the Cytiva Discovery Consumables business to all segments within Denmark, Sweden, Norway and Iceland. Success in the role requires very active promotion of our products and solutions in the field, to end-users such as lab managers, bench scientists, group leaders and procurement. The Consumer Sales Specialist will be responsible for consumable product lines within the research area of protein purification and characterization (Western blotting), laboratory filtration, and nucleic acid purification and amplification while leveraging sales via our network of distributor partners.
This position is part of the Discovery Commercial team and will be fully remote. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
What you will do:
Achieve sales targets and customer satisfaction by developing and maintaining high level knowledge of product portfolio while building customer relationships following key funding opportunities within key accounts. Lead sales negotiation and deal closure, interfacing with all key buying influencers such as direct users and decision makers
Create end user demand for both direct / indirect customers in the field, including driving and partnering with our distributors to promote Cytiva consumables. Promote solution selling by combining consumables in the customer workflow and find leads for related instruments
Develop long-term relationships with key internal stakeholders (Account Managers, Sales Specialists, Product Managers) within your region helping develop sales of the entire Cytiva portfolio.
Work closely with Zone Leaders and Channel Managers to identify key distributor needs and act as a customer advocate internally to align the business to those needs; monitor performance of distributor network within the territory and develop / implement action plans to achieve maximum revenue and margin impact; and attend regular distributor reviews, hold product and business presentations and provide training where requested.
Actively use CRM system (Salesforce.com) to ensure transparency and funnel management



Who you are:
Degree qualified and minimum two years commercial sales experience of working in the field of Life Sciences with knowledge of life sciences industry and marketplace trends
Demonstrated ability to analyze customer data and develop financially sound sales solutions. 2+ years of consultative sales experience
Proficiency in computer skills including Microsoft Office Suite products, CRM systems such as Salesforce, and QlikSense
Fluent English and Swedish/Danish language skills, written and verbal
Ability to travel (by car and plane) within the geographic region three days per week, including overnight stays as required Visa mindre

Scrum Master

Ansök    Okt 28    Cytiva Sweden AB    Mjukvaruutvecklare
Bli en del av något helt livsavgörande Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier. Som del av Cytiva får du möjlighet att utveckla dig själv och oss – du kommer att bidra ti... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier.
Som del av Cytiva får du möjlighet att utveckla dig själv och oss – du kommer att bidra till att lösa utmaningar som har verklig betydelse för människors hälsa tillsammans med kollegor som bryr sig om varandra, våra kunder och deras patienter.
Med medarbetare i över 40 länder är Cytiva en arbetsplats där varje dag är en möjlighet att lära sig mer – så att du kan fortsätta växa i din karriär och stärka dina färdigheter över tid.
BioProcess R&D Software består av drygt 90 personer och ansvarar för mjukvaruutvecklingen inom BioProcess Downstream området. Vår största mjukvara UNICORN används av kromatografi-, cellodling- och filtreringsystem för styrning, övervakning och avancerad analys.
Vi söker en Scrum Master till ett av våra team inom R&D BioProcess Software. Som Scrum Master har du en nyckelroll i arbetet med att leda mjukvaruutvecklingen på Cytiva och förbättra våra arbetssätt kring hur vi på ett effektivt sätt utvecklar mjukvara av hög kvalitet. Vill du vara med och utveckla mjukvara för bioteknologiska produkter som används inom läkemedelsforskning och produktion i hela världen? Då vill vi att du hör av dig!
Dina arbetsuppgifter:
I rollen som Scrum Master kommer du leda ett tvärfunktionellt team som ansvarar för hela utvecklingsprocessen från kravspecificering till implementation och test samt verifiering. Product discovery, automatiserad enhetstestning, TDD (Test Driven Design) och BDD (Behavior Driven Design) är en integrerad del av arbetssättet.
Leda teamet inom agila metoder och driva kontinuerliga förbättringar inom teamet och avdelningen.
Utveckla ett starkt samarbete med andra utvecklarteam i en större skalad agil miljö.
Coacha och stötta produktägare.
Hjälpa teamet med Azure DevOps och andra agila verktyg.
Driva och assistera teamet att uppnå sina leveransmål.
Dela information om teamets totala prestation, kontinuerligt mäta och förbättra flöde, kvalitet, kundvärde.
Bidra till utvecklingsarbetet i teamet i mån av tid.

De huvudsakliga kraven för tjänsten är:
Relevant universitetsutbildning (MSc / BSc Software Engineering, Computer Science, eller liknande) eller motsvarande arbetslivserfarenhet.
Erfarenhet från liknande roll som scrum master eller agil coach.
God erfarenhet och stort intresse av agila metoder.
Erfarenhet av mjukvaruutveckling med tonvikt på C#/.NET.
Erfarenhet av produktutveckling och en förståelse av en produkts livscykel.
Vana att jobba inom ett kvalitetssystem och ha förståelse för dess vikt för att säkerställa plattformens framtida kvalitet.
Kommunicerar flytande på både svenska och engelska.

Det är även meriterande om du har:
Erfarenhet av GAMP5 inklusive 21 CFR Part 11.
Vana av TDD (Test Driven Design) och BDD (Behavior Driven Design).
Erfarenhet av att ha varit releaseansvarig för en mjukvaruprodukt (exempelvis agile release manager).
Erfarenhet av AWS och HTML5.

Stor vikt kommer att läggas vid den ansökandes personlighet, professionella intressen och driv.?Vi söker dig som har ett stort intresse för agila metoder och hur man bygger effektiva och självgående team. Du är trygg både i din tekniska kompetens och ledarskapsförmåga samt bekväm i att samarbeta brett och tvärfunktionellt med andra för att hitta lösningar och nå resultat.
Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. För frågor rörande tjänsten vänligen kontakta rekryterande chef Ulrika Öhman [email protected]. Välkommen med din ansökan! Visa mindre

Senior Electronics Engineer

Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
We are now looking for a Senior Electronics Engineer to strengthen our hardware team in Uppsala. You will be a part of a team of engineers within electronics, optics and cyber security. You will be involved in the development and improvement of our chromatography systems. You will have varying tasks and responsibilities and will be involved in the entire development process taking ideas from the drawing board all the way to production.
In this role, you will have the opportunity to:
Design, develop, and sustain electrical systems and instrumentation. Evaluate and problem-solve electrical systems, products, components, and applications, applying knowledge of electricity and materials. Includes Electromechanical subsystems.
Ensure reliability, performance and delivery through relationships with both internal and external manufacturing and supplier base.
Engage in product care and sustaining engineering including concept, architecture documentation, design, prototype, test, supplier interfaces, manufacturing and service support
Design and document test plans & outcomes
Participate in technical reviews and collaborative technical forums
Plan for and maintain required test equipment and laboratory equipment

The essential requirements of the job include:
BSc. or MSc in Electrical Engineering, or equivalent.
Long-standing experience in product development and/or sustaining engineering
Multiple years of experience with some of the following: Product/System Design, Analog, digital and/or mixed signal development, Analog/digital system modeling and analysis, EMC, ESD, Grounding, and motion controls or power electronics
Previous experience with eCAD tools, OrCAD preferred.
Fluent in both Swedish and English languages (written and verbal)

Interviews and selections take place continuously, so don't wait to send in your application.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Scientist, Analysis

Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
We are looking for a Scientist to join the Viral Vector Applications section in the Genomics Medicine OpCo at R&D in Uppsala. The section is made up by 12 researchers that are working in the areas of protein purification, filtration and analysis of viral vectors, plasmids, and nuclei acids, working with product development to get the right products to the customers. We are now looking for an expert in analytical methods used for AAV (focus ELISA/qPCR).
What you'll do:
As a Scientist you will be an expert in analytical methods that are needed for analysis of titer/viral genomes content for viral vectors via ELISA, qPCR, ddPCR etc.
Work will be conducted in new product development, product care and market support projects with customer needs in focus.
You will be conducting analysis work in various projects. This includes being involved in method development and method verification as well as maintaining instrumentation and creating standard operating procedures and work close to QA and production with validations of analytical methods.
It is important that you in addition to technical expertise can independently plan and perform the tasks in a structured way, report the results at project meetings and in customer discussions. You will also be expected to present posters and orals at conferences occasionally.

Who you are:
You have a PhD or MSc with a few years’ experience from a diverse set of analytical methods with focus on qPCR and ELISA, preferably toward Viral vectors in the biopharmaceutical field or a PhD in relevant field with some industry experience.
You have extensive experience in different analysis methods (ELISA, qPCR, BiaCore, Gyros) for both cell culture, filtrated and purified AAV. It’s meritorious if you have worked with other analysis tools/equipment's with viral vectors, for ex DLS, Refeyn, MALS, HPLC.
Experience of filtration of biomolecules would be advantageous as well as some knowledge in cell culture work.
You have validation and method development expertise
Interaction and communication with colleagues will be key in this role and you should enjoy working in a flexible and dynamic environment. Demonstrated abilities to work in a collaborative and customer focused setting.
Strong presentation and communications skills are important. Advanced English (oral and writing) and working proficiency in Swedish language.
Valid Swedish work permit.

Application
We continuously assess candidates and invite them for interviews, so please don’t hesitate to write and send in the application before 7th of November. However the recruitment will be completed as soon as suitable candidate is found. We look forward to seeing your application. Visa mindre

Business Process Specialist

Ansök    Okt 16    Cytiva Sweden AB    Systemansvarig
Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
As Business Process Specialist you will be an integrated part of the global PDM team and interact seamlessly with functional- and IT teams on a global level. You will contribute to development of continuous improvement activities in the PDM area across organizations and systems.
The Life Sciences Product Data Management team is responsible for process and system governance of the global processes for product registration, sales/order stop, phase out and discontinuation. We also manage the global user support and training for the Magic application and product registration.
The Business Process Specialist position is part of the Product Data Management team located in Uppsala, Sweden and the UK and will be an on-site role. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
In this role, you will have the opportunity to:
Work in cross-functional teams to define wing-to-wing system requirements, to implement standard processes and optimize process flows - all in alignment with global PDM strategies and governing principles.
Support functional teams in product data management related matters, including W2W issue analysis and resolution with attention to urgency.
Create and maintain user documentation & training material and deliver training to business users.
Perform analysis and extracting/loading activities related to data migration.
Collaborate with global IT to develop, test and deliver system enhancements and defect fixes.
Perform analysis of data consistency across systems. Plan, coordinate and execute updates and communication/follow-up.

The essential requirements of the job include:
Bachelor's degree in engineering or Life Sciences or similar.
??Background from R&D/Engineering/Product Development?.
Process oriented and strong analytical skills with an interest to understand and interpret customer business needs and translate them into user and application requirements.?
??Experience working with PLM or ERP systems.
??Interest and ability to work with cross-functional, multi-cultural teams and deliver results in an ambiguous- and dynamic environment.?
Fluency in English both written & oral communication.

It would be a plus if you also possess previous experience in:
Enovia-MAGIC

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Senior Manager IT R&D PMO

Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The Senior Manager IT R&D PMO at Cytiva is responsible for ensuring that IT R&D projects and portfolios are effectively managed to achieve organizational goals.
This position is part of the IT R&D department which is an Enterprise Organization with a global presence. This specific position is located in Uppsala Sweden (but with global responsibility) and will be an onsite position. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
In this role, you will have the opportunity to:
Strategic Alignment: Ensuring that projects and portfolios align with the organization's strategic objectives.
Risk Management: Identifying, assessing, and mitigating risks across projects and portfolios.
Performance Monitoring and Reporting: Collecting, analyzing, and reporting project performance data accurately.
Organizational Politics: Operate within complex organizational structures with competing priorities and power dynamics.
Complexity and Scale: Managing large, complex project portfolios with interdependencies and diverse stakeholders.
Technological Advancements: Keeping up with rapidly evolving project management technologies and methodologies.
Talent Management: Recruiting, retaining, and developing skilled project management professionals.

The essential requirements of the job include:
Bachelor's or Master's degree in Computer Science, Software Engineering, or a related field.
Several years of proven and documented People Management experience.
Experience in leading projects, familiarity with project management tools and software, and relevant certifications (such as PMP, PRINCE2, or Agile certifications) demonstrate proficiency in project management.
Effective communication and stakeholder management skills. (proficient English language skills is a must)

It would be a plus if you also possess previous experience in:
Proven GxP knowledge
Industry knowledge within Life science/Bioprocessing/Chemical/Process industry.
Financial Management including:
Financial Reporting/Business Case Development/ Vendor and Contract Management/Benefits Realization/ Financial Governance and Compliance

At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Utvecklingsingenjör, Process Technology

Bli en del av något helt livsavgörande Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell-och genterapier. På Cytiva kommer du att ständigt kunna utveckla dig själv och oss -genom att arbeta... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell-och genterapier.
På Cytiva kommer du att ständigt kunna utveckla dig själv och oss -genom att arbeta med utmaningar som verkligen spelar roll tillsammans med människor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i 40 länder är Cytiva en plats där varje dag är en möjlighet att lära så att du kan få fart på din karriär och förbättra dina färdigheter på lång sikt.
Vi på Cytiva är stolta över att arbeta tillsammans med en grupp av nio andra Danaher Life Sciences-företag. Tillsammans är vi pionjärer inom vetenskap och medicin och utvecklar produkter som hjälper forskare i kampen att rädda liv.
Just nu söker vi efter vår nästa utvecklingsingenjör med inriktning Process Technology till sektionen Advanced Manufacturing Engineering (AME) på Cytivas site i Uppsala. Sektionen består av utvecklingsingenjörer, operatörer, teamleaders och sektionschef som tillsammans verkar för att utveckla och utvärdera morgondagens tillverkningsprocesser för separationsmedia på Cytiva. Som utvecklingsingenjör hos oss har du en flexibel och varierad arbetsdag med ansvar för allt från kunskapsinhämtning till försökskörningar i lab-, pilot- och produktionsskala. Har du ett intresse för process- och produktionsutveckling och erfarenhet av att jobba med processförbättringar och optimeringar? Då vill vi gärna höra från dig!
Att arbeta som AME är varierande och roligt och passar dig som söker en central roll inom förtaget med nära samarbeten med Produktion, FoU, Product Management och EHS. Du kan exempelvis arbeta med ständiga förbätt­ringar och att optimera produk­tions­pro­cesser, att identifiera och eliminera onödiga kostnader, kvali­tets­säkring eller att imple­mentera ny teknik/kemi i produktion.
De huvudsakliga kraven för tjänsten är:
Agera områdesexpert för Process Technology-applikationer inom Cytivas BioProcess-område.
Utveckla, utvärdera och implementera förbättrade tillverkningsprocesser och strategier i produktionen.
Arbeta tillsammans med FoU, Product Management, EHS och produktionen för att identifiera grundorsaken till problem och möjligheter kopplade till metoder, processer, utrustning och produktdesign.
Agera expert inom produktionsteknik i tidigt skede under NPI-projekt för att säkerställa att bästa tekniken används.
Planera, förbereda, genomföra, utvärdera och dokumentera försök i lab-, pilot- eller produktionsskala.

De huvudsakliga kraven för tjänsten är:
Civilingenjör inom kemiteknik, fysik, maskinteknik eller motsvarande utbildningsbakgrund.
Kunskap om processindustriella processer/enhetsoperationer och tekniker.
Kommunicerar väl muntligt och skriftligt på både engelska och svenska.
Tjänsten erbjuder stora möjligheter för dig som är självgående och initiativtagande!

Det är även meriterande om du har:
Projektledningserfarenhet.
Erfarenhet av processförbättringar/optimering i processindustriella miljöer
Stort teknikintresse och är resultatorienterad

För att vara framgångsrik i rollen som utvecklingsingenjör ser vi gärna att du som söker är en kommunikativ person som trivs med att jobba både självständigt och i grupp. Vidare ser vi gärna att du har en förmåga att självständigt driva ditt arbete framåt och ta egna initiativ. Du har ett stort tekniskt intresse och öga för detaljer.
Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. För frågor rörande tjänsten vänligen kontakta rekryterande chef Vollmer Bomfim [email protected]. Varmt välkommen med din ansökan!
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Engineering Graduate Program - Lead System Designer

Engineering Graduate Program - Lead System Designer Are you ready to embark on an exciting journey that will kick-start your career and empower you to have a real impact in transforming human health worldwide? With a rich heritage dating back hundreds of years, our wealth of technical expertise and talent, a broad and deep portfolio, and exceptional service help researchers and biopharma advance therapeutics at every stage from discovery to delivery. At Cy... Visa mer
Engineering Graduate Program - Lead System Designer
Are you ready to embark on an exciting journey that will kick-start your career and empower you to have a real impact in transforming human health worldwide? With a rich heritage dating back hundreds of years, our wealth of technical expertise and talent, a broad and deep portfolio, and exceptional service help researchers and biopharma advance therapeutics at every stage from discovery to delivery. At Cytiva, our mission is to advance and accelerate therapeutics. Our vision is a world in which access to life-changing therapies transforms human health.
We are currently seeking passionate and ambitious talents to join our Engineering Graduate Program in Uppsala, starting January 2025. The Engineering Graduate Program is divided into different engineering profiles. Together with us, you will be at the forefront of enabling our customers in the development, manufacturing, and delivery of transformative medicines to patients. As an Engineering Graduate at Cytiva, you will benefit from:
Develop and accelerate your technical knowledge and expertise together with a team of young professionals.
Opportunities for cross-functional project work, site visits, and internal training sessions to learn about Cytiva’s core technologies and business.
Exposure to a global network of talented colleagues through regular interaction with team members, managers, and project teams.
Growth and development through mentorship from experienced professionals and managers.
Stability from a permanent position at Cytiva.

What we’re looking for:
We’re looking for ambitious graduate talents who are excited to join us in our quest to advance and accelerate therapeutics. To be eligible for Cytiva’s Engineering Graduate Program, we require that you meet the following criteria:
Hold a relevant university degree in engineering, technology, or a related field.
Enthusiastic and eager to learn and grow within the Life Science engineering field.
Strong communication skills in English.
Interactive team player that is comfortable working in project teams collaborating with colleagues to solve problems and find solutions.

About the role: Lead System Designer
As Lead System Designer at Cytiva, you will work in a dynamic environment in cross functional project teams transforming requirements and customer needs into products. You will contribute with technical knowhow and continuously build your skillset and experience with support from your functional peers. In addition, you have a central role in all parts of the product development life cycle and will work closely with Mechanical and Electrical Engineers, Automation Designers and Verification Engineers to deliver results.
In this role, you will have the opportunity to:
Deliver customized Bioprocess equipment.
Translate requirement specifications into design specifications.
Identify and select functional components such as pumps, valves, pressure sensors, flow meters and other instrumentation as needed.
Define main functions and create functional specifications.
Participate and support regulatory compliance activities.
Establish acceptance criteria for the final product.
Perform/participate in internal design reviews.
Participate in customer design reviews and present design solutions for customers.

Application:
The Engineering Graduate Program will accept applications until the 30th of November. In your application, please include your resume and cover letter. For any questions regarding the specific role, please contact hiring manager Joakim Eklund, Sr Manager - Functional Design, [email protected]. Visa mindre

Engineering Graduate Program - Electrical Engineer

Engineering Graduate Program - Electrical Engineer Are you ready to embark on an exciting journey that will kick-start your career and empower you to have a real impact in transforming human health worldwide? With a rich heritage dating back hundreds of years, our wealth of technical expertise and talent, a broad and deep portfolio, and exceptional service help researchers and biopharma advance therapeutics at every stage from discovery to delivery. At Cyt... Visa mer
Engineering Graduate Program - Electrical Engineer
Are you ready to embark on an exciting journey that will kick-start your career and empower you to have a real impact in transforming human health worldwide? With a rich heritage dating back hundreds of years, our wealth of technical expertise and talent, a broad and deep portfolio, and exceptional service help researchers and biopharma advance therapeutics at every stage from discovery to delivery. At Cytiva, our mission is to advance and accelerate therapeutics. Our vision is a world in which access to life-changing therapies transforms human health.
We are currently seeking passionate and ambitious talents to join our Engineering Graduate Program in Uppsala, starting January 2025. The Engineering Graduate Program is divided into different engineering profiles. Together with us, you will be at the forefront of enabling our customers in the development, manufacturing, and delivery of transformative medicines to patients. As an Engineering Graduate at Cytiva, you will benefit from:
Strong support to develop and accelerate your technical knowledge and expertise together with a team of young professionals.
Opportunities for cross-functional project work, site visits, and internal training sessions to learn about Cytiva’s core technologies and business.
Exposure to a global network of talented colleagues through regular interaction with team members, managers, and project teams.
Growth and development through mentorship from experienced professionals and managers.
Stability from a permanent position at Cytiva.

What we’re looking for:
We’re looking for ambitious graduate talents who are excited to join us in our quest to advance and accelerate therapeutics. To be eligible for Cytiva’s Engineering Graduate Program, we require that you meet the following criteria:
Hold a relevant university degree in engineering, technology, or a related field.
Enthusiastic and eager to learn and grow within the Life Science engineering field.
Strong communication skills in English.
Interactive team player that is comfortable working in project teams collaborating with colleagues to solve problems and find solutions for our customers.

About the role: Electrical Engineer
As Electrical Engineer at Cytiva, you become an integral part of our engineering team, working under the guidance of experienced professionals. This role offers a unique opportunity to gain in-depth knowledge and practical experience in electrical engineering while at the same time learning about Cytiva’s core technologies and products. Upon completion of the program, you will have gained a solid foundation to continue to shape your career at Cytiva.
In this role, you will have the opportunity to:
Support the design of electrical cabinets for our large-scale chromatography systems, ensuring compliance with industry standards and safety regulations.
Work with senior engineers to systemize, select appropriate components and create electrical schematics.
Assist in the assembly, testing and troubleshooting of prototypes in our own labs.
Collaborate with cross-functional teams, including mechanical engineers, software developers, and project managers.
Maintain accurate and up-to-date project documentation, including design files, test reports, and technical manuals.
Assist in enhancements to tools and ways of working.

Application:
The Engineering Graduate Program will accept applications until the 30th of November. In your application, please include your resume and cover letter. For any questions regarding the specific role, please contact Mikael Hörnqvist, Principal Electronics Engineer, [email protected]. Visa mindre

Engineering Graduate Program - R&D Software Engineer, Test Automation

Ansök    Okt 14    Cytiva Sweden AB    Mjukvaruutvecklare
Engineering Graduate Program - R&D Software Engineer, Test Automation Are you ready to embark on an exciting journey that will kick-start your career and empower you to have a real impact in transforming human health worldwide? With a rich heritage dating back hundreds of years, our wealth of technical expertise and talent, a broad and deep portfolio, and exceptional service help researchers and biopharma advance therapeutics at every stage from discovery ... Visa mer
Engineering Graduate Program - R&D Software Engineer, Test Automation
Are you ready to embark on an exciting journey that will kick-start your career and empower you to have a real impact in transforming human health worldwide? With a rich heritage dating back hundreds of years, our wealth of technical expertise and talent, a broad and deep portfolio, and exceptional service help researchers and biopharma advance therapeutics at every stage from discovery to delivery. At Cytiva, our mission is to advance and accelerate therapeutics. Our vision is a world in which access to life-changing therapies transforms human health.
We are currently seeking passionate and ambitious talents to join our Engineering Graduate Program in Uppsala, starting January 2025. The Engineering Graduate Program is divided into different engineering profiles. Together with us, you will be at the forefront of enabling our customers in the development, manufacturing, and delivery of transformative medicines to patients. As an Engineering Graduate at Cytiva, you will benefit from:
Strong support to develop and accelerate your technical knowledge and expertise together with a team of young professionals.
Opportunities for cross-functional project work, site visits, and internal training sessions to learn about Cytiva’s core technologies and business.
Exposure to a global network of talented colleagues through regular interaction with team members, managers, and project teams.
Growth and development through mentorship from experienced professionals and managers.
Stability from a permanent position at Cytiva.

What we’re looking for:
We’re looking for ambitious graduate talents who are excited to join us in our quest to advance and accelerate therapeutics. To be eligible for Cytiva’s Engineering Graduate Program, we require that you meet the following criteria:
Hold a relevant university degree in engineering, technology, or a related field.
Enthusiastic and eager to learn and grow within the Life Science engineering field.
Strong communication skills in English.
Interactive team player that is comfortable working in project teams collaborating with colleagues to solve problems and find solutions for our customers.

About the role: R&D Software Engineer, Test Automation
As a Software Engineer within Test Automation at Cytiva, you’ll work with your own and adjacent software development teams in an agile and dynamic environment. Together with your peers, you will strive to ensure that the software delivered for system testing maintains a consistently high quality through a combination of manual and automated tests. You’ll contribute with skills and build your experience in close collaboration with colleagues across the organization. You’ll participate and contribute to all parts of the software development life cycle. Eventually, you’ll be able to contribute with customer case management.
In this role, you will have the opportunity to:
Early-stage quality assurance through software testing.
Software test automation through design and implementation of automated test cases.
Strategic decision about test cases suitable for manual and automated tests.
Test case coverage and presentation of automated test result.
Development of automated tests template and test support to the development teams.
Manual testing, both at instruments and through simulators.
Test documentation.

Application:
The Engineering Graduate Program will accept applications until the 30th of November. In your application, please include your resume and cover letter. For any questions regarding the specific role, please contact hiring manager Petter Lönnstedt, Sr Manager - Process Instrument Software, [email protected]. Visa mindre

Engineering Graduate Program - Electrical Design Engineer

Engineering Graduate Program - Electrical Design Engineer Are you ready to embark on an exciting journey that will kick-start your career and empower you to have a real impact in transforming human health worldwide? With a rich heritage dating back hundreds of years, our wealth of technical expertise and talent, a broad and deep portfolio, and exceptional service help researchers and biopharma advance therapeutics at every stage from discovery to delivery.... Visa mer
Engineering Graduate Program - Electrical Design Engineer
Are you ready to embark on an exciting journey that will kick-start your career and empower you to have a real impact in transforming human health worldwide? With a rich heritage dating back hundreds of years, our wealth of technical expertise and talent, a broad and deep portfolio, and exceptional service help researchers and biopharma advance therapeutics at every stage from discovery to delivery. At Cytiva, our mission is to advance and accelerate therapeutics. Our vision is a world in which access to life-changing therapies transforms human health.
We are currently seeking passionate and ambitious talents to join our Engineering Graduate Program in Uppsala, starting January 2025. The Engineering Graduate Program is divided into different engineering profiles. Together with us, you will be at the forefront of enabling our customers in the development, manufacturing, and delivery of transformative medicines to patients. As an Engineering Graduate at Cytiva, you will benefit from:
Strong support to develop and accelerate your technical knowledge and expertise together with a team of young professionals.
Opportunities for cross-functional project work, site visits, and internal training sessions to learn about Cytiva’s core technologies and business.
Exposure to a global network of talented colleagues through regular interaction with team members, managers, and project teams.
Growth and development through mentorship from experienced professionals and managers.
Stability from a permanent position at Cytiva.

What we’re looking for:
We’re looking for ambitious graduate talents who are excited to join us in our quest to advance and accelerate therapeutics. To be eligible for Cytiva’s Engineering Graduate Program, we require that you meet the following criteria:
Hold a relevant university degree in engineering, technology, or a related field
Enthusiastic and eager to learn and grow within the Life Science engineering field.
Strong communication skills in English.
Interactive team player that is comfortable working in project teams collaborating with colleagues to solve problems and find solutions for our customers.

About the role: Electrical Design Engineer
As an Electrical Design Engineer at Cytiva, you will take part of the Custom Engineering onsite team, providing electrical design support to the business and its staff to deliver customized bioprocess equipment to customers worldwide.
In this role, you will have the opportunity to:
Create electrical design for our products according to customer specifications in a global market. Including activities such as doing the design ready for production in our PLM system.
Identification and development of design solutions, design in 2D/3D for cabinet, production of drawings, selection of components including specifications, contact with subcontractors to verify technical data, administer article data and create components in CAD programs (EPLAN, AutoCAD), documentation of product structures.
Work in a project organization where each customer order becomes its own project with resources from project management, system design, detailed design, production preparation, purchasing and verification.
Participate in final inspection/testing of electrical equipment according to scope communicated by project manager.
Support Installation, troubleshooting, diagnosing and update documentation.
Responsible for carrying out their work according to the agreed schedule and to the right scope according to the needs of the project.

Application:
The Engineering Graduate Program will accept applications until the 30th of November. In your application, please include your resume and cover letter. For any questions regarding the specific role, please contact hiring manager Björn Haglund, Sr Manager - Mechanical Design, [email protected]. Visa mindre

Engineering Graduate Program – Automation Engineer

Ansök    Okt 14    Cytiva Sweden AB    Mjukvaruutvecklare
Engineering Graduate Program – Automation Engineer Are you ready to embark on an exciting journey that will kick-start your career and empower you to have a real impact in transforming human health worldwide? With a rich heritage dating back hundreds of years, our wealth of technical expertise and talent, a broad and deep portfolio, and exceptional service help researchers and biopharma advance therapeutics at every stage from discovery to delivery. At Cyt... Visa mer
Engineering Graduate Program – Automation Engineer
Are you ready to embark on an exciting journey that will kick-start your career and empower you to have a real impact in transforming human health worldwide? With a rich heritage dating back hundreds of years, our wealth of technical expertise and talent, a broad and deep portfolio, and exceptional service help researchers and biopharma advance therapeutics at every stage from discovery to delivery. At Cytiva, our mission is to advance and accelerate therapeutics. Our vision is a world in which access to life-changing therapies transforms human health.
We are currently seeking passionate and ambitious talents to join our Engineering Graduate Program in Uppsala, starting January 2025. The Engineering Graduate Program is divided into different engineering profiles. Together with us, you will be at the forefront of enabling our customers in the development, manufacturing, and delivery of transformative medicines to patients. As an Engineering Graduate at Cytiva, you will benefit from:
Strong support to develop and accelerate your technical knowledge and expertise together with a team of young professionals.
Opportunities for cross-functional project work, site visits, and internal training sessions to learn about Cytiva’s core technologies and business.
Exposure to a global network of talented colleagues through regular interaction with team members, managers, and project teams.
Growth and development through mentorship from experienced professionals and managers.
Stability from a permanent position at Cytiva.

What we’re looking for:
We’re looking for ambitious graduate talents who are excited to join us in our quest to advance and accelerate therapeutics. To be eligible for Cytiva’s Engineering Graduate Program, we require that you meet the following criteria:
Hold a relevant university degree in engineering, technology, or a related field.
Enthusiastic and eager to learn and grow within the Life Science engineering field.
Strong communication skills in English.
Interactive team player that is comfortable working in project teams collaborating with colleagues to solve problems and find solutions for our customers.

About the role: Automation Engineer
As an Automation Engineer at Cytiva, you will work with your team in a dynamic and cross functional environment. You will contribute with your technical skills and build your experience in close collaboration with colleagues. You will participate and contribute to all parts of the automation software development life cycle, transforming requirements and customer needs into products.
In this role, you will have the opportunity to:
Development and maintenance of automation software for bioprocess systems.
PLC programming for Rockwell and potentially other platforms.
Control systems development.
Development in Rockwell Studio 5000 and similar tools.
Contribute to technical documentation.
Maintenance and development of internal tools and simulation and test environments.

Application:
The Engineering Graduate Program will accept applications until the 30th of November. In your application, please include your resume and cover letter. For any questions regarding the specific role, please contact hiring manager Anders Wessman, Section Manager - Automation, [email protected]. Visa mindre

Engineering Graduate Program - Verification Engineer

Engineering Graduate Program - Verification Engineer Are you ready to embark on an exciting journey that will kick-start your career and empower you to have a real impact in transforming human health worldwide? With a rich heritage dating back hundreds of years, our wealth of technical expertise and talent, a broad and deep portfolio, and exceptional service help researchers and biopharma advance therapeutics at every stage from discovery to delivery. At C... Visa mer
Engineering Graduate Program - Verification Engineer
Are you ready to embark on an exciting journey that will kick-start your career and empower you to have a real impact in transforming human health worldwide? With a rich heritage dating back hundreds of years, our wealth of technical expertise and talent, a broad and deep portfolio, and exceptional service help researchers and biopharma advance therapeutics at every stage from discovery to delivery. At Cytiva, our mission is to advance and accelerate therapeutics. Our vision is a world in which access to life-changing therapies transforms human health.
We are currently seeking passionate and ambitious talents to join our Engineering Graduate Program in Uppsala, starting January 2025. The Engineering Graduate Program is divided into different engineering profiles. Together with us, you will be at the forefront of enabling our customers in the development, manufacturing, and delivery of transformative medicines to patients. As an Engineering Graduate at Cytiva, you will benefit from:
Strong support to develop and accelerate your technical knowledge and expertise together with a team of young professionals.
Opportunities for cross-functional project work, site visits, and internal training sessions to learn about Cytiva’s core technologies and business.
Exposure to a global network of talented colleagues through regular interaction with team members, managers, and project teams.
Growth and development through mentorship from experienced professionals and managers.
Stability from a permanent position at Cytiva.

What we’re looking for:
We’re looking for ambitious graduate talents who are excited to join us in our quest to advance and accelerate therapeutics. To be eligible for Cytiva’s Engineering Graduate Program, we require that you meet the following criteria:
Hold a relevant university degree in engineering, technology, or a related field.
Enthusiastic and eager to learn and grow within the Life Science engineering field.
Strong communication skills in English.
Interactive team player that is comfortable working in project teams collaborating with colleagues to solve problems and find solutions for our customers.

About the role: Verification Engineer
As Verification Engineer at Cytiva, you will work with your team in a dynamic and cross functional environment. You will contribute with your skills and at the same time build your knowledge in close collaboration with colleagues under the guidance of our experienced professionals. You will participate in the verification process, transforming requirements and customer needs into new components and into new product development. The role offers a unique opportunity to gain in-depth knowledge and practical experience in physical verification engineering while learning about Cytiva’s core technologies and products.
In this role, you will have the opportunity to:
Support testing of instrument prototypes in our labs. Troubleshooting, diagnosing and contributing to technical documentation.
Collaborate with cross-functional teams within R&D, including mechanical engineers, system engineers and project managers.
Assist in the enhancement to tools and ways of working to expedite results.
Keep track of customer needs and test requirements.
Development and maintenance of equipment and instruments for testing bioprocess systems.

Application:
The Engineering Graduate Program will accept applications until the 30th of November. In your application, please include your resume and cover letter. For any questions regarding the specific role, please contact hiring manager Magnus Emerius, Sr Manager - ÄKTA Instrument Engineering, [email protected]. Visa mindre

Engineering Graduate Program – Automation Engineer

Ansök    Okt 14    Cytiva Sweden AB    Mjukvaruutvecklare
Engineering Graduate Program – Automation Engineer Are you ready to embark on an exciting journey that will kick-start your career and empower you to have a real impact in transforming human health worldwide? With a rich heritage dating back hundreds of years, our wealth of technical expertise and talent, a broad and deep portfolio, and exceptional service help researchers and biopharma advance therapeutics at every stage from discovery to delivery. At Cyt... Visa mer
Engineering Graduate Program – Automation Engineer
Are you ready to embark on an exciting journey that will kick-start your career and empower you to have a real impact in transforming human health worldwide? With a rich heritage dating back hundreds of years, our wealth of technical expertise and talent, a broad and deep portfolio, and exceptional service help researchers and biopharma advance therapeutics at every stage from discovery to delivery. At Cytiva, our mission is to advance and accelerate therapeutics. Our vision is a world in which access to life-changing therapies transforms human health.
We are currently seeking passionate and ambitious talents to join our Engineering Graduate Program in Uppsala, starting January 2025. The Engineering Graduate Program is divided into different engineering profiles. Together with us, you will be at the forefront of enabling our customers in the development, manufacturing, and delivery of transformative medicines to patients. As an Engineering Graduate at Cytiva, you will benefit from:
Strong support to develop and accelerate your technical knowledge and expertise together with a team of young professionals.
Opportunities for cross-functional project work, site visits, and internal training sessions to learn about Cytiva’s core technologies and business.
Exposure to a global network of talented colleagues through regular interaction with team members, managers, and project teams.
Growth and development through mentorship from experienced professionals and managers.
Stability from a permanent position at Cytiva.

What we’re looking for:
We’re looking for ambitious graduate talents who are excited to join us in our quest to advance and accelerate therapeutics. To be eligible for Cytiva’s Engineering Graduate Program, we require that you meet the following criteria:
Hold a relevant university degree in engineering, technology, or a related field.
Enthusiastic and eager to learn and grow within the Life Science engineering field.
Strong communication skills in English.
Interactive team player that is comfortable working in project teams collaborating with colleagues to solve problems and find solutions for our customers.

About the role: Automation Engineer
As an Automation Engineer at Cytiva, you will work with your team in a dynamic and cross functional environment. You will contribute with your technical skills and build your experience in close collaboration with colleagues. You will participate and contribute to all parts of the automation software development life cycle, transforming requirements and customer needs into products.
In this role, you will have the opportunity to:
Development and maintenance of automation software for bioprocess systems.
PLC programming for Rockwell and potentially other platforms.
Control systems development.
Development in Rockwell Studio 5000 and similar tools.
Contribute to technical documentation.
Maintenance and development of internal tools and simulation and test environments.

Application:
The Engineering Graduate Program will accept applications until the 30th of November. In your application, please include your resume and cover letter. For any questions regarding the specific role, please contact hiring manager Anders Wessman, Section Manager - Automation, [email protected]. Visa mindre

Engineering Graduate Program – Automation Engineer

Ansök    Okt 14    Cytiva Sweden AB    Mjukvaruutvecklare
Engineering Graduate Program – Automation Engineer Are you ready to embark on an exciting journey that will kick-start your career and empower you to have a real impact in transforming human health worldwide? With a rich heritage dating back hundreds of years, our wealth of technical expertise and talent, a broad and deep portfolio, and exceptional service help researchers and biopharma advance therapeutics at every stage from discovery to delivery. At Cyt... Visa mer
Engineering Graduate Program – Automation Engineer
Are you ready to embark on an exciting journey that will kick-start your career and empower you to have a real impact in transforming human health worldwide? With a rich heritage dating back hundreds of years, our wealth of technical expertise and talent, a broad and deep portfolio, and exceptional service help researchers and biopharma advance therapeutics at every stage from discovery to delivery. At Cytiva, our mission is to advance and accelerate therapeutics. Our vision is a world in which access to life-changing therapies transforms human health.
We are currently seeking passionate and ambitious talents to join our Engineering Graduate Program in Uppsala, starting January 2025. The Engineering Graduate Program is divided into different engineering profiles. Together with us, you will be at the forefront of enabling our customers in the development, manufacturing, and delivery of transformative medicines to patients. As an Engineering Graduate at Cytiva, you will benefit from:
Strong support to develop and accelerate your technical knowledge and expertise together with a team of young professionals.
Opportunities for cross-functional project work, site visits, and internal training sessions to learn about Cytiva’s core technologies and business.
Exposure to a global network of talented colleagues through regular interaction with team members, managers, and project teams.
Growth and development through mentorship from experienced professionals and managers.
Stability from a permanent position at Cytiva.

What we’re looking for:
We’re looking for ambitious graduate talents who are excited to join us in our quest to advance and accelerate therapeutics. To be eligible for Cytiva’s Engineering Graduate Program, we require that you meet the following criteria:
Hold a relevant university degree in engineering, technology, or a related field.
Enthusiastic and eager to learn and grow within the Life Science engineering field.
Strong communication skills in English.
Interactive team player that is comfortable working in project teams collaborating with colleagues to solve problems and find solutions for our customers.

About the role: Automation Engineer
As Automation Engineer at Cytiva, you will work with your team in a dynamic and cross functional environment. You will contribute with skills and build your experience in close collaboration with colleagues. You will participate and contribute to all parts of the automation software development life cycle, transforming requirements and customer needs into products.
In this role, you will have the opportunity to:
Design and maintain automation software tailored for bioprocess systems.
Program and configure systems using DeltaV software.
Engage with Siemens DCS platform projects.
Create documentation alongside the software development process.
Collaborate with project teams to ensure successful automation deliverables.
Participate in customer meetings and facilitate customer communications.
Develop and upkeep internal tools, as well as simulation and testing environments.

Application:
The Engineering Graduate Program will accept applications until the 30th of November. In your application, please include your resume and cover letter. For questions regarding this position, please contact hiring manager Sophie Guo [email protected]. Visa mindre

Engineering Graduate Program – Automation Engineer

Ansök    Okt 14    Cytiva Sweden AB    Mjukvaruutvecklare
Engineering Graduate Program – Automation Engineer Are you ready to embark on an exciting journey that will kick-start your career and empower you to have a real impact in transforming human health worldwide? With a rich heritage dating back hundreds of years, our wealth of technical expertise and talent, a broad and deep portfolio, and exceptional service help researchers and biopharma advance therapeutics at every stage from discovery to delivery. At Cyt... Visa mer
Engineering Graduate Program – Automation Engineer
Are you ready to embark on an exciting journey that will kick-start your career and empower you to have a real impact in transforming human health worldwide? With a rich heritage dating back hundreds of years, our wealth of technical expertise and talent, a broad and deep portfolio, and exceptional service help researchers and biopharma advance therapeutics at every stage from discovery to delivery. At Cytiva, our mission is to advance and accelerate therapeutics. Our vision is a world in which access to life-changing therapies transforms human health.
We are currently seeking passionate and ambitious talents to join our Engineering Graduate Program in Uppsala, starting January 2025. The Engineering Graduate Program is divided into different engineering profiles. Together with us, you will be at the forefront of enabling our customers in the development, manufacturing, and delivery of transformative medicines to patients. As an Engineering Graduate at Cytiva, you will benefit from:
Strong support to develop and accelerate your technical knowledge and expertise together with a team of young professionals.
Opportunities for cross-functional project work, site visits, and internal training sessions to learn about Cytiva’s core technologies and business.
Exposure to a global network of talented colleagues through regular interaction with team members, managers, and project teams.
Growth and development through mentorship from experienced professionals and managers.
Stability from a permanent position at Cytiva.

What we’re looking for:
We’re looking for ambitious graduate talents who are excited to join us in our quest to advance and accelerate therapeutics. To be eligible for Cytiva’s Engineering Graduate Program, we require that you meet the following criteria:
Hold a relevant university degree in engineering, technology, or a related field.
Enthusiastic and eager to learn and grow within the Life Science engineering field.
Strong communication skills in English.
Interactive team player that is comfortable working in project teams collaborating with colleagues to solve problems and find solutions for our customers.

About the role: R&D Automation Engineer
As Automation Engineer at Cytiva, you will work with your team in a dynamic and cross-functional environment. You will contribute with skills and build your experience in close collaboration with colleagues. You will participate and contribute to all parts of the automation software development life cycle, transforming requirements and customer needs into products.
In this role, you will have the opportunity to:
Development and maintenance of automation software for bioprocess systems.
PLC programming for Rockwell and potentially other platforms.
Control systems development.
Development in Rockwell Studio 5000 and similar tools.
Contribute to technical documentation.
Maintenance and development of internal tools and simulation and test environments.

Application:
The Engineering Graduate Program will accept applications until the 30th of November. In your application, please include your resume and cover letter. For any questions regarding the specific role, please contact hiring manager Petter Lönnstedt, Sr Manager - Process Instrument Software, [email protected]. Visa mindre

Engineering Graduate Program – Automation Engineer

Ansök    Okt 14    Cytiva Sweden AB    Mjukvaruutvecklare
Engineering Graduate Program – Automation Engineer Are you ready to embark on an exciting journey that will kick-start your career and empower you to have a real impact in transforming human health worldwide? With a rich heritage dating back hundreds of years, our wealth of technical expertise and talent, a broad and deep portfolio, and exceptional service help researchers and biopharma advance therapeutics at every stage from discovery to delivery. At Cyt... Visa mer
Engineering Graduate Program – Automation Engineer
Are you ready to embark on an exciting journey that will kick-start your career and empower you to have a real impact in transforming human health worldwide? With a rich heritage dating back hundreds of years, our wealth of technical expertise and talent, a broad and deep portfolio, and exceptional service help researchers and biopharma advance therapeutics at every stage from discovery to delivery. At Cytiva, our mission is to advance and accelerate therapeutics. Our vision is a world in which access to life-changing therapies transforms human health.
We are currently seeking passionate and ambitious talents to join our Engineering Graduate Program in Uppsala, starting January 2025. The Engineering Graduate Program is divided into different engineering profiles. Together with us, you will be at the forefront of enabling our customers in the development, manufacturing, and delivery of transformative medicines to patients. As an Engineering Graduate at Cytiva, you will benefit from:
Strong support to develop and accelerate your technical knowledge and expertise together with a team of young professionals.
Opportunities for cross-functional project work, site visits, and internal training sessions to learn about Cytiva’s core technologies and business.
Exposure to a global network of talented colleagues through regular interaction with team members, managers, and project teams.
Growth and development through mentorship from experienced professionals and managers.
Stability from a permanent position at Cytiva.

What we’re looking for:
We’re looking for ambitious graduate talents who are excited to join us in our quest to advance and accelerate therapeutics. To be eligible for Cytiva’s Engineering Graduate Program, we require that you meet the following criteria:
Hold a relevant university degree in engineering, technology, or a related field.
Enthusiastic and eager to learn and grow within the Life Science engineering field.
Strong communication skills in English.
Interactive team player that is comfortable working in project teams collaborating with colleagues to solve problems and find solutions for our customers.

About the role: Automation Engineer
As Automation Engineer at Cytiva, you will work with your team in a dynamic and cross functional environment. You will contribute with skills and build your experience in close collaboration with colleagues. You will participate and contribute to all parts of the automation software development life cycle, transforming requirements and customer needs into products.
In this role, you will have the opportunity to:
Design and maintain automation software tailored for bioprocess systems.
Program and configure systems using DeltaV software.
Engage with Siemens DCS platform projects.
Create documentation alongside the software development process.
Collaborate with project teams to ensure successful automation deliverables.
Participate in customer meetings and facilitate customer communications.
Develop and upkeep internal tools, as well as simulation and testing environments.

Application:
The Engineering Graduate Program will accept applications until the 30th of November. In your application, please include your resume and cover letter. For questions regarding this position, please contact hiring manager Sophie Guo [email protected]. Visa mindre

Automation Engineer

Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
We're looking for a Senior Automation Engineer to join the Custom Engineering department at our site in Uppsala. Custom Engineering is a global organization within Cytiva that delivers customized equipment, instrumentation and solutions to our customers around the world. As Senior Automation Engineer at Custom Engineering, you will be part of and contribute to our positive and dynamic delivery focused culture. Each customer order becomes a project, delivered by a cross-functional team focused on meeting our customers high expectations in lead-time and quality.
This position is part of the Custom Engineering located in Uppsala and will be an on-site role. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
What you’ll do
As Senior Automation Engineer at Custom Engineering, you are responsible for the automation design of our products. You will make use of your strong collaboration skills working in cross functional project teams transforming customer needs into deliverables. Your genuine interest in technology and curiosity to develop and learn is essential for you excelling in this role.
In addition to product development will you also make use of your automation engineering skills supporting the sales and quotation organization, the service organization and the QC organization in testing and FAT.
In this role, you will have the opportunity to:
Develop and maintain PLC code and configurations for bioprocess systems.
Design and create P&ID;:s and other documentation.
Support Sales and Quotation, Service, QC and other colleagues within Custom Engineering.

The essential requirements of the job include:
BSc or MSc in Automation Engineering, Electronics or similar.
Experience in Rockwell/Allen-Bradley tools such as Studio5000 and ACM.
Experience in programming Codesys.
Experience and knowledge in automation engineering related tasks such as establishing requirements specifications and writing technical reports.
Experience in different industrial field bus technologies (EtherNet/IP, Profibus, OPC UA/DA)
Professional level English skills, both written and oral. Fluency in Swedish is a great advantage.

It would be a plus if you also possess previous experience in:
Developing software code using languages such as C#, JavaScript, Python or others
AutoCAD software.
Other automation platforms than Rockwell.
UNICORN control software.
Working in the biotech industry.

To be successful in this role, we're looking for an energized and results-oriented self-starter with great communication skills. Whether you're a seasoned engineer or newly graduated isn't the most important, what matters is your drive and passion for automation design and technology.
At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Scientist - Computational Chromatography Resin Ligand Design

Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The Scientist - Computational Chromatography Resin Ligand Design at Cytiva will apply the most recent advances in in Silico prediction of protein-protein interactions using Artificial Intelligence to the design of new affinity chromatographic ligands, speeding up Cytiva’s ligand development and offering faster new tools to our customers.
This position is part of the Resin and Technology Unit that is located in Uppsala, Sweden. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
What you will do:
The successful candidate will apply state-of-the-art AI powered protein/peptide structure prediction and protein-protein or protein-peptide or peptide-peptide interaction algorithms and simulation techniques to generate in silico ligand leads towards chosen targets. The role will be part of a team that will validate the new ligands in a laboratory setting.
You will also contribute to the implementation of the AI capacity within Cytiva’s organization
It is expected that you are fully aware of the latest advances in the field such as RF diffusion modelling

Who you are:
The applicant must hold a PhD degree in the field of Biophysics or Biochemistry or Computational aided rational design.
Demonstrated skills in computational biochemistry and particularly in software such as RF diffusion model, Rosetta or Alpha/ESM Fold or the like
Track record of scientific accomplishment demonstrated by peer-reviewed publications
The applicant must have an excellent scientific expertise in the latest developments in machine learning and AI powered tools
Very good oral and written proficiency in English.

It would be a plus if you also possess previous experience in:
Good ability to manage own priorities and deliverables, both independently and in the team setting
Working knowledge of protein structure and protein protein interactions

?
Application
We continuously assess candidates and invite them for interviews, so please don’t hesitate to write and send in the application. The recruitment will be completed as soon as a suitable candidate is found. If you have questions, feel free to contact: [email protected]
We look forward to seeing your application.
At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Service Diagnostics Engineer

Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The Service Diagnostics Engineer for Cytiva is responsible for developing our Diagnostic development program for internal and external diagnostics to enable remote troubleshooting and diagnostics. This role will be tightly integrated with both our internal product development teams as well as our field service organization.
This position is part of the Service R&D Organization located in Uppsala, Sweden and will be an on-site role. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
In this role, you will have the opportunity to:
Champions Diagnostics Modelling techniques, gathering voice of the customer information from both Field Service Engineers and Manufacturing Test Technicians
As a key member of Service R&D Digital team, creates and maintains diagnostics methodologies and architectures for new product launches
Incorporates Diagnostics requirements in Product Lifecycle Management processes and documents to ensure that projects are resourced to deliver on Diagnostic requirements
Works with R&D, system engineering, and project design teams at early stages of a project (pre-concept phase) to incorporate design for service and improve diagnostics capability.
Reviews new designs and ECOs for compliance to diagnostics requirements and provides feedback on diagnostic capabilities to system engineers and designers
Work with Domain Engineers and to identify and leverage alerts/fault messages which can serve to better isolate symptoms to root causes and optimize the resolution and detection of problem trends
Works in conjunction with 3rd party suppliers and 3rd party engineering groups to ensure “hooks” are available for diagnostics tools to interrogate and monitor status and fault of OEM modules.
Builds Failure Models (using Designer resources) to load into Diagnostics Tools that produce Fault Tree paths to root cause
Determines service requirements for diagnostics and ease of system troubleshooting on new products during the product development cycle.
Conducts troubleshooting/technical workshops with cross functional teams and collects best practices for service process/troubleshooting improvement.
Improves speed and accuracy for root cause failure determination for installed products
Identifies areas for new Standard Work activity
Other duties as assigned

The essential requirements of the job include:
B.S. or higher degree in a scientific discipline. Training in Engineering or Science – preference to Systems or Electrical engineering
Strong interpersonal skills; effective at collaborating and building consensus
Requires minimum 5+ years of experience working with Product Development project teams, or equivalent experience in product related R&D, Systems or Architecture design, deployment of Diagnostics programs/ tools etc.
Ability to read schematics and engineering drawings and high-level understanding of relevant technologies (electrical, electromechanical etc.)
Experience with executing Fault Tree Analysis, Reliability Block Diagrams
Strong troubleshooting and problem solving skills.
Interpersonal and leadership skills to effectively work with teams in the investigation of real or potential problems and development of action plans to resolve them.
Continuous improvement aptitude
Effective peer communication skills

It would be a plus if you also possess previous experience in:
Familiar with diagnostic software applications and tools
Biotechnology/Life Sciences industry
GMP & regulatory environments
QMS and Documentation Practices

Application
We continuously assess candidates and invite them for interviews, so please don’t hesitate to write and send in the application. The recruitment will be completed as soon as a suitable candidate is found.
If you have questions, feel free to contact the hiring manager Padma Malladi [email protected]
We look forward to seeing your application.
At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Additive Process Engineer

Be part of something altogether life-changing Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us –working on challenges that truly ... Visa mer
Be part of something altogether life-changing
Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us –working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity –so you can grow your career and expand your skills in the long term.
Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.
We are looking for an Additive Design Engineer to join our dynamic Additive Manufacturing (AM) team, which is part of our Bioprocess Central Technology Organization, supporting all businesses and functions within Cytiva. The team is responsible for driving the scientific and technology agenda within the AM field, providing support and expertise to new product development and R&D teams across Cytiva. This position is an onsite role, based at our site in Uppsala, Sweden, and is a temporary position (until September 2025).
What you will do:
Drive Design for Additive, and support build-up of capability in the global Cytiva organization. Engage in training of design engineers and manufacturing engineers.
Contribute with expertise on CAD design and adjacent technical solutions.
Work closely with R&D teams in all Cytiva business units: independently lead, perform, and support design for additive activities in projects – from idea and concept development, via prototyping, to transfer to production.
Evaluate and implement new additive technologies and materials, both polymer and metal.
Provide hands-on support in 3D printing and post-processing work – to understand how design and production processes are interconnected, and how both can be improved.

The essential requirements of the job include:
BSc or MSc in Mechanical Engineering, or equivalent educational background.
A few years experience working with mechanical design.
Strong working knowledge of CAD software (e.g. Creo, SolidWorks) and file management.
Experience of additive manufacturing (3D printing), alternatively experience of CNC machining and/or injection molding.
Fluency in English – both written and verbal.

It would be a plus if you also have:
Proven ability to lead small technical projects.
Fluency in Swedish – both written and verbal.

To be successful in this role, the ideal candidate should be an excellent communicator with strong interpersonal skills, possess a creative mindset, focus on customer needs, excel in cross-functional collaboration.
Interview and selection will happen continuously, and the opening can be filled before last day of application, October 6th. For questions regarding the role please contact hiring manager Bo Medhage, Director - Additive Manufacturing, [email protected]. Welcome in with your application!
At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Human Resources Director - Nordics

Ansök    Sep 16    Cytiva Sweden AB    HR-chef
Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The HR Director – Nordics for Cytiva will play a critical role in aligning human resource strategies with business objectives to drive performance and growth. This strategic leadership role requires a deep understanding of business functions, strong HR expertise, and the ability to influence and drive change. The Director will partner with senior leadership and management teams across the Nordics to develop and implement HR solutions that enhance organizational capability and support the achievement of business goals. The HR Director will lead a Nordic team of 8 HR professionals such as Senior HR Business partners and HR specialists.
This position is part of the EMEA HR Leadership team in Cytiva located in Uppsala Sweden and will be an onsite position. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
What you will do:
Strategic HR Partnership
Act as a trusted advisor and partner to the Site leader and their teams, understanding site needs and ensuring a consistent approach across the region. Collaborate with Business Leaders, Global HR Business Partners and their teams to identify and address organizational and employee-related issues.
HR Strategy and Execution
Develop and implement Country HR plans and initiatives that align with business strategies and drive organizational effectiveness. Lead key HR projects and initiatives across the Nordics and the wider EMEA HR team, ensuring alignment with corporate goals and timelines.
Talent Management & Diversity, Equity and Inclusion (DEI)
Work in partnership with Global HR Business Partners to ensure a consistent approach across the region to talent management processes, including succession planning, talent development and performance management. Promote and support diversity, equity, and inclusion initiatives within the organization, partnering with leaders to develop and implement programs that foster an inclusive workplace culture.
Employee Relations
Work closely with the Labor and Employee Relations Leader to strengthen relationships with works councils and ensure adherence to co-determination and collective bargaining agreement (CBA) compliance. Foster a positive work environment and address employee concerns effectively. Ensure compliance with all relevant employment laws and regulations.
Change Management
Lead HR aspects of organizational change, including restructures, mergers and acquisitions as appropriate. Develop and implement change management strategies to ensure smooth transitions and minimize disruption.
HR Metrics and Analysis
Utilize HR data and analytics to inform decision-making and measure the effectiveness of HR initiatives. Prepare and present reports on key HR metrics and trends to senior leadership.
Coach, engage and develop HR team across Nordics
Creating an environment of career development and succession planning
Who you are:
Master or Bachelor’s Degree in Human Resources or Business Studies
Strong knowledge of Employee Relations/legal compliance and experience of working with works councils.
Minimum of 8 years’ experience working in a Senior HR Business Partner position within a Manufacturing environment.
Proven leadership experience and demonstrated ability to collaborate cross-functionally in a matrixed organization.
Experience of leading change management programmes in a fast-paced, regulated and matrixed global organisation.
Outstanding client service orientation: ability to maintain confidentiality and handle sensitive situations with solid judgement and discretion
Has strong orientation to accomplishing objectives in a measurable and sustainable way, recognizing obstacles while utilizing resources to overcome these, helping self and others to achieve results.
Fluent in written and verbal communication - Swedish and English

Travel, Motor Vehicle Record & Physical/Environment Requirements:
Must be willing to travel across Nordics to perform role and across EMEA as required. Visa mindre

Drifttekniker - Reningsverk & Miljösektionen

Ansök    Sep 16    Cytiva Sweden AB    Kemitekniker
Hjälp oss att förbättra tillgången till livsavgörande behandlingar som kan förändra människors hälsa Vi är Cytiva, en global leverantör av teknologier och tjänster som främjar och påskyndar utvecklingen och tillverkningen av terapier. Våra kunder bedriver livsavgörande forskning och produktion, alltifrån biologisk forskning till utveckling av nya vacciner, läkemedel, cell- och genterapier. Vårt uppdrag är att leverera verktygen och tjänsterna som de behö... Visa mer
Hjälp oss att förbättra tillgången till livsavgörande behandlingar som kan förändra människors hälsa
Vi är Cytiva, en global leverantör av teknologier och tjänster som främjar och påskyndar utvecklingen och tillverkningen av terapier.


Våra kunder bedriver livsavgörande forskning och produktion, alltifrån biologisk forskning till utveckling av nya vacciner, läkemedel, cell- och genterapier. Vårt uppdrag är att leverera verktygen och tjänsterna som de behöver, allt för att kunna leverera snabbare och säkrare vård till patienter.

Vi söker en Drifttekniker till Reningsverk & Miljö sektionen inom Kemisk Produktion Uppsala. Vi ansvarar för drift och tillgänglighet för reningsanläggningar, utför mätningar av luft- och vattenemissioner och säkerställer efterlevnad av krav på utsläppen, samt kartlägger vattenströmmar för att minska miljöpåverkan.

Dina arbetsuppgifter
Provtagning, provhantering, drift och underhåll av reningsanläggningar.
Utför regelbunden rondering och underhållsarbeten samt utför kalibreringar av olika instrument.
Delta i projekt som berör sektionen , jobba med ständiga förbättringar samt delta i EHS-relaterade ärenden.
Vidta åtgärder för att förhindra oförutsedda utsläpp till omgivningsmiljön.


I tjänsten ingår jourberedskap kvällar och helger enligt schema.

Vem är du
Erfarenhet från styrsystem eller övervakning av processer
Goda kunskaper i svenska och engelska.
Som person är du driven, tar egna initiativ och bekväm vid att fatta beslut. Du har god problemlösningsförmåga och trivs med att arbeta självständigt och i grupp.


Tidigare erfarenheter anses meriterande
Erfarenhet från Reningsverk och/eller inom processindustri.
Erfarenhet från kemikaliehantering och Ex-miljö.


Välkommen in med din ansökan! Visa mindre

Servicetekniker till Underhållssektionen

Bli en del av något helt livsavgörande Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier. På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbe... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier.
På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbeta med utmaningar som verkligen spelar roll tillsammans med människor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i 40 länder är Cytiva en plats där varje dag är en möjlighet att lära så att du kan få fart på din karriär och förbättra dina färdigheter på lång sikt.
Vi på Cytiva är stolta över att arbeta tillsammans med en grupp av nio andra Danaher Life Sciences-företag. Tillsammans är vi pionjärer inom vetenskap och medicin och utvecklar produkter som hjälper forskare i kampen att rädda liv.
Vi söker nu en Servicetekniker till underhållssektionen på Cytivas site i Uppsala. Vår sektion består av 28 medarbetare som tillsammans ansvarar för fortlöpande tillsyn, underhåll och utveckling av sitens processutrustning. Tjänsterna inom sektionen består av styr- och reglertekniker, underhållsmekaniker, serviceingenjör, underhållsingenjör och underhållsspecialister. Som Servicetekniker hos oss ansvarar du för att service och underhåll av sitens processutrustning. Tjänsten är en tillsvidareanställning på heltid.
Dina arbetsuppgifter:
Utföra felsökningar och reparationer på produktionsutrustning.
Utföra förebyggande och avhjälpande underhållsinsatser.
Administration och avrapportering av utförd service av underhållssystemet.
Beställa material kopplat till arbetsordrar.
Stödja och utbilda operatörer i frågor gällande underhåll, skötsel och tillsyn av produktionsutrustningar.

De huvudsakliga kraven för tjänsten är:
Treårig teknisk gymnasieutbildning eller motsvarande flerårig yrkesvana.
Svetsteknisk kunskap inom främst TIG-svetsning.
Goda kunskaper inom området pumpar, ventiler, mekanik, hydraulik och pneumatik.
Erfarenhet av liknande arbetsuppgifter inom läkemedels-, livsmedels eller medicinteknikbranschen.
Du kommunicerar flytande på svenska och engelska i både tal och skrift.

Det är även meriterande om du har också har:
Kvalificerad yrkesutbildning inom relevant fokusområde, t.ex processautomation, process eller underhållsteknik.
Erfarenhet av datoriserade underhållsprogram.

För att trivas i rollen bör du ha ett brett tekniskt intresse. Du är serviceinriktad och säkerhetsmedveten med förmåga att driva flera aktiviteter samtidigt med högt ansvarstagande. Det är också viktigt att du kan arbeta strukturerat, är noggrann och har god förmåga att samarbeta i grupp. Vid denna rekrytering kommer vi att lägga stor vikt vid dina personliga egenskaper.
Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. För frågor rörande den här tjänsten vänligen kontakta rekryterande chef Martin Frick, Senior Manager - Maintenance, [email protected]. Varmt välkommen med din ansökan! Visa mindre

Valideringsingenjör

Ansök    Sep 11    Cytiva Sweden AB    Valideringsingenjör
Bli en del av något helt livsavgörande Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier. På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbe... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier.
På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbeta med utmaningar som verkligen spelar roll tillsammans med människor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i 40 länder är Cytiva en plats där varje dag är en möjlighet att lära så att du kan få fart på din karriär och förbättra dina färdigheter på lång sikt.
Vi på Cytiva är stolta över att arbeta tillsammans med en grupp av nio andra Danaher Life Sciences-företag. Tillsammans är vi pionjärer inom vetenskap och medicin och utvecklar produkter som hjälper forskare i kampen att rädda liv.
Vi söker nu en valideringsingenjör till avdelningen Manufacturing Engineering som är en del av vår storskaliga kemiska produktionsverksamhet i Uppsala. Valideringsgruppen, som är en sektion inom avdelningen Manufacturing Engineering, består idag av 16 valideringsingenjörer som arbetar mot vår produktion vid ombyggnationer, nya installationer, process- och styrsystemsändringar.
Produktionen i Uppsala omfattar ett flertal olika tillverkningsavdelningar och som valideringsingenjör hos oss får du möjlighet till varierade arbetsuppgifter och att växa i din yrkesroll.
Dina arbetsuppgifter:
Planera, utforma och genomföra valideringar.
Arbeta med utveckling och förbättringar.
Granska/bedöma kravspecifikationer, riskbedömningar och ändringsärenden.
Presentera valideringsdokumentation vid audit.

De huvudsakliga kraven för tjänsten är:
Teknisk/Naturvetenskaplig universitetsexamen, gärna civilingenjör eller motsvarande.
Erfarenhet från bioteknik-, läkemedels- eller processindustri.
Mycket goda kunskaper i svenska och engelska, såväl muntligt som skriftligt.

Det är även meriterande om du har tidigare erfarenhet av:
Goda kunskaper om valideringsarbete.
Erfarenhet av validering inom tex datoriserade/automationssystem inom produktion, vattenvalidering, rengöringsvalidering, processvalidering samt installations- och funktionskvalificering.

För rollen som valideringsingenjör söker vi dig som är drivande och ansvarstagande i ditt arbete. Som person har du god förmåga att analysera problem och generera kreativa lösningar. Du är flexibel, har lätt för att samarbeta samtidigt som du är van att arbeta självständigt. Du är serviceinriktad med stor integritet. Arbetet förutsätter också att du är strukturerad med en naturlig förmåga att beskriva valideringars syfte och resultat på ett tydligt och överskådligt sätt.
Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. För frågor rörande den här tjänsten vänligen kontakta rekryterande chef Therese Håfström på [email protected]. Varmt välkommen med din ansökan! Visa mindre

Kalibreringsingenjör

Bli en del av något helt livsavgörande Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier. På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbe... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier.
På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbeta med utmaningar som verkligen spelar roll tillsammans med människor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i 40 länder är Cytiva en plats där varje dag är en möjlighet att lära så att du kan få fart på din karriär och förbättra dina färdigheter på lång sikt.
Vi på Cytiva är stolta över att arbeta tillsammans med en grupp av nio andra Danaher Life Sciences-företag. Tillsammans är vi pionjärer inom vetenskap och medicin och utvecklar produkter som hjälper forskare i kampen att rädda liv.
Vi söker nu en Kalibreringsingenjör till underhållssektionen på Cytivas site i Uppsala. Vår sektion består av 28 medarbetare som tillsammans ansvarar för fortlöpande tillsyn, underhåll och utveckling av sitens processutrustning. Tjänsterna inom sektionen består av styr- och reglertekniker, underhållsmekaniker, serviceingenjör, underhållsingenjör och underhållsspecialister. Som Kalibreringsingenjör hos oss ansvarar du för kalibrering och service av sitens processutrustning. Tjänsten är en tillsvidareanställning på heltid med jourberedskap var 6:e vecka.
Dina arbetsuppgifter:
Kalibrering av mätinstrument som ligger inom ramen för sektionens ansvar.
In- och urkoppling av elektriska processutrustningar.
Uppdatering av systembeskrivningar, kretsscheman och elscheman i CAD.
Felsökning på processutrustning.
Förebyggande och avhjälpande underhåll på processutrustningar.
Särskilt ansvar för ATEX-direktiven på Underhållssektionen.

De huvudsakliga kraven för tjänsten är:
Treårig gymnasieutbildning med styr- och reglerteknik, elektronik och el.
Goda kunskaper inom automationsområden som styr- och reglerteknik, mekanik, elektronik, hydraulik, och/eller pneumatik.
Du kommunicerar flytande på svenska och engelska i både tal och skrift.

Det är även meriterande om du har också har:
Goda kunskaper om processteknisk utrustning.
Kunskap eller erfarenhet av CAD, särkilt ELCAD.

För att trivas i rollen bör du ha ett brett tekniskt intresse. Du är serviceinriktad och säkerhetsmedveten med förmåga att driva flera aktiviteter samtidigt med högt ansvarstagande. Det är också viktigt att du kan arbeta strukturerat, är noggrann och har god förmåga att samarbeta i grupp. Vid denna rekrytering kommer vi att lägga stor vikt vid dina personliga egenskaper.
Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. För frågor rörande den här tjänsten vänligen kontakta rekryterande chef Martin Frick, Senior Manager - Maintenance, [email protected]. Varmt välkommen med din ansökan! Visa mindre

Regulatory Support Manager

Be part of something altogether life-changing Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care ... Visa mer
Be part of something altogether life-changing
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
We’re looking for a Regulatory Support Manager to join Cytiva’s Customer Regulatory Support (CRS) team at our site in Uppsala. As Regulatory Support Manager, focusing on our chromatography resin product portfolio, you are responsible for providing support to Product Managers, Regions and customers by providing quality documents and regulatory support in response to customers’ requests for quality, regulatory and technical-related information. As a member of the Customer Regulatory Support team, you will add value to bioprocess products and demonstrate a commitment to customer satisfaction.
What you´ll do:
Build and maintain knowledge and understanding of customers’ regulatory requirements related to the bioprocess business at a high level.
Develop and update regulatory support documentation for products in customers’ regulated environments.
Perform necessary investigations and prepare and deliver statements and certificates.
Participate in creating and updating guidelines and steering documents.
Act as regulatory support expert and discussion partner to R&D, QA, Product Management and other functions and regions.
Participate in project teams as regulatory support expert.
Respond efficiently and promptly to customers’ regulatory based issues, which will include necessary investigations, preparations and delivery of certificates, use of available internal and external databases and other relevant databases.
File and maintain complete documentation of questions and answers in databases; specify, prepare, update and review regulatory support documentation, including RSF, VG, VSF, CCN, statements, certificates and other regulatory related documentation for new and existing products.

The essential requirements of the job include:
Bachelor of Science degree in Chemistry, Pharmacy or related field.
A few years of experience from relevant positions within Quality Assurance, Regulatory, or Product Management.
Good understanding of GMP and knowledge of regulatory requirements in the bioprocess industry.
Excellent communication skills and fluency in English, both written and spoken.

It would be a plus if you also have:
Experience of working in large matrix organizations.
Fluency in the language of the country of employment.
Experience in customer communication.

We are seeking a candidate who is organized, accurate, and target-oriented, with a strong focus on quality and customer service. The ideal candidate should be flexible, service-minded, and able to collaborate effectively across teams.
Interview and selection will happen continuously, and the opening can be filled before last day of application. For questions regarding the role please contact hiring manager Henrik Norberg, Senior Manager Customer Regulatory Support, [email protected]. We look forward to hearing from you!
At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Produktionsingenjör

Bli en del av något helt livsavgörande Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier. På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbe... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier.
På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbeta med utmaningar som verkligen spelar roll tillsammans med människor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i 40 länder är Cytiva en plats där varje dag är en möjlighet att lära så att du kan få fart på din karriär och förbättra dina färdigheter på lång sikt.
Vi på Cytiva är stolta över att arbeta tillsammans med en grupp av nio andra Danaher Life Sciences-företag. Tillsammans är vi pionjärer inom vetenskap och medicin och utvecklar produkter som hjälper forskare i kampen att rädda liv.
Vill du vara del av ett starkt team där du kan påverka din vardag på jobbet? Vill du ha ett varierande arbete där du får arbeta praktiskt men även utvecklas med teknologiska lösningar? Är du en engagerad och nyfiken person som letar efter nästa utmaning? Då kan du vara den nya medarbetare som vi söker!
Arbetsuppgifter
Vi söker en Produktionsingenjör till sektionen Kolonnproduktion och är en del av den kemiska produktionen på vår site i Uppsala. Gruppen består av både operatörer och ingenjörer som tillsammans tillverkar kromatografikolonner i labskala på 15 olika produktionslinor. Kolonnproduktionen är en del av den kemiska produktionen inom Cytiva. Rollen som produktionsingenjör på Cytiva innebär framför allt att du är ett dagligt stöd till produktionen. Rent praktiskt kan det innebära att du arbetar med att:
Driva Change Control-ärenden och avvikelsehantering.
Teknisk felsökning av processutrustning.
Kontakt med underhållsavdelning och/eller entreprenörer.
Samarbeta med F&U vid nyproduktprojekt och produktvårdsprojekt.
Agera som stöd i reklamationsärenden och driva utredningar rörade reklamationer.

Du driver även förbättringsarbete, uppdaterar produktionsdokument samt utför och dokumenterar riskanalyser mm. Ingenjörsarbetet präglas av variation och en möjlighet till att påverka den dagliga verksamheten, där tillverkningen står i fokus.
De huvudsakliga kraven för tjänsten är:
Civilingenjör eller motsvarande med inriktning mot bioteknik/kemiteknik/maskinteknik eller liknande utbildningsbakgrund.
Du behärskar svenska och engelska flytande i tal och skrift.
God datorvana och trygg användare av olika IT-system.

Det är även meriterande om du har tidigare erfarenhet av:
Goda kunskaper om process- och produktutveckling.
Erfarenhet av att beräkna och optimera kapacitet samt resursbehov och förbrukning, i olika typer av produktionsavsnitt.
Tidigare erfarenhet av kolonnpackning.

För att vara framgångsrik i denna roll ser vi gärna att du är en lagspelare med god samarbetsförmåga och att du trivs i med att jobba både med teknik och med människor. Vidare ser vi gärna att du är en säkerhets- och kvalitetsmedveten person med god förmåga att ta initiativ och driva flera parallella aktiviteter samtidigt.
Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. För frågor rörande den här tjänsten vänligen kontakta rekryterande chef Martina Brolin [email protected]. Varmt välkommen med din ansökan! Visa mindre

R1267818 Global Service Readiness Engineer

Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that ca... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The Global Service Readiness Engineer for Cytiva is responsible for ensuring high serviceability standards in new product development- & lifecycle-management projects, technical publications, initial training, global parts availability, and service process validation
This position is part of the Global Service Readiness Engineering Team located in Uppsala, Sweden and will be hybrid. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
What you will do:
Support the service organization in new product development- & life-cycle management projects to become a technical subject matter expert
Supports Global Service Strategy Projects
Verify and validate global service procedures and improvement activities through lab-testing, design reviews and data evaluation




Who you are:
University Degree in Engineering: e.g. Biomedical, Mechatronics, Systems-Engineering, or comparable qualification through work-experience
Hands-on approach with regards to installations, upgrades and repairs
Understanding of technical writing
Fluently English language skills



It would be a plus if you also possess previous experience in:
Demonstrated technical depth with problem-solving techniques and meeting deadlines & deliverables
Experience in field service engineering, project engineering, systems engineering
Fluently Swedish language skills


At Cytiva we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, hybrid working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a hybrid work arrangement in which you can work part-time at the Company location identified above and part-time remotely from your home. Additional information about this hybrid work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide. Visa mindre

Riskingenjör

Bli en del av något helt livsavgörande Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier. På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbe... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier.
På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbeta med utmaningar som verkligen spelar roll tillsammans med människor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i 40 länder är Cytiva en plats där varje dag är en möjlighet att lära så att du kan få fart på din karriär och förbättra dina färdigheter på lång sikt.
Vi på Cytiva är stolta över att arbeta tillsammans med en grupp av nio andra Danaher Life Sciences-företag. Tillsammans är vi pionjärer inom vetenskap och medicin och utvecklar produkter som hjälper forskare i kampen att rädda liv.
Vi söker nu efter vår nästa riskingenjör till avdelningen Environment, Health and Safety (EHS) på Cytivas anläggning i Uppsala. Som riskingenjör hos oss ingår du i det lokala EHS-teamet bestående av ett 20-tal experter inom områdena processäkerhet, arbetsmiljö, yttre miljö och kemikaliehantering. Tillsammans verkar vi för en säker och hållbar arbetsplats med lägsta möjliga klimatavtryck. Har du ett intresse för processäkerhetsfrågor och vill bli del av ett tvärfunktionellt team med flera spännande kontaktytor på en Seveso-klassad produktionsanläggning? Då vill vi gärna höra från dig!
Som riskingenjör hos oss ansvarar du för att säkerställa att processerna följer säkerhetsbestämmelser och standarder, identifiera och bedöma potentiella säkerhetsrisker, utveckla och implementera säkerhetsåtgärder, samt övervaka och rapportera om säkerhetsfrågor. Rollen innebär även att samarbeta med olika team för att förbättra säkerheten och att utbilda personalen i säkerhetsprocedurer.
Dina arbetsuppgifter
Arbeta med riskhantering för processystem i syfte att förhindra olyckor som brand, explosion och okontrollerat utflöde från anläggningar som hanterar farliga ämnen.
Genomföra olika typer av riskanalyser så som Hazid, Hazop, SWIFT, grovriskanalys m.m.
Arbeta i ett team för process säkerhet med att utveckla och förbättra företagets rutiner som har processäkerhetspåverkan.
Delta i projektarbete med att definiera konstruktionskrav och följa upp dessa.
Vara en del i EHS teamets compliance kontroll, via lagbevakning och aktiviteter för att kontrollera lagefterlevnad på företaget.
Delta i Cytivas arbete för ständiga förbättringar, via till exempel hantering av händelserapporter, både lokalt och i globala sammanhang.
Föra dialog med externa aktörer, så som myndigheter och försäkringsbolag.
Utveckla instruktioner och hålla i utbildningar inom processäkerhetsområdet.

De huvudsakliga kraven för tjänsten är:
Lämplig utbildningsbakgrund är risk-, brand- eller civilingenjörsexamen inom ett för tjänsten relevant område.
Ett par års erfarenhet av från kemisk/teknisk processindustri eller liknande.
Kunnig om säkerhetspraxis, analysmetoder och regelverk inom området.
Erfarenhet av riskhantering- och olycksutredningsmetodik.
Du kommunicerar obehindrat på såväl svenska som på engelska, både i tal och i skrift.

Det är även meriterande om du har tidigare erfarenhet av:
Utbildningsbakgrund med inriktning mot kemi eller kemiteknik.
Förtrogen med kravtolkning utifrån styrande lagar som tex Seveso, LBE, LSO och AML-lagstiftningen.

Vi ser gärna att du som söker är organiserad, arbetar med struktur och har en god förmåga att förankra och förklara dina beslut. Det är viktigt att du som person trivs i att coacha och ge stöd till verksamheten i risk- och processäkerhetsfrågor. Du arbetar självständigt, är initiativtagande och uppskattar samverkan med andra.
Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. För frågor rörande den här tjänsten vänligen kontakta rekryterande chef Sigrid de Geyter, EHS Director, på [email protected]. Varmt välkommen med din ansökan! Visa mindre

Scientist – Protein purification and resin characterization

Ansök    Aug 29    Cytiva Sweden AB    Kemiingenjör
Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
We are looking for a Scientist to work in our Affinity Ligand characterization team within the R&D Resins and Technologies business unit at Cytiva. The team is responsible for characterization and application work of new chromatography products. The team is also responsible for development of analytical methods to characterize biomolecules such as new protein ligands. This position is based in Uppsala, Sweden and will be an on-site role.
What you will do:
Plan, perform, document and present laboratory experiments for characterization of chromatography products. The work includes evaluation of purification performance, dynamic binding capacity and alkaline stability of new chromatography products using ÄKTA chromatography systems.
Provide technical expertise within the areas of purification of proteins and/or other biomolecules. Solve technical problems, supporting both Research, Development and QC related projects.
Act as a mentor/local expert and support peers within the area of characterization and application of chromatography products.
Present scientific and technical results internally and externally, oral and written communication in Swedish and English.

The essential requirements of the job include:
PhD in Microbiology/Biochemistry or related Life Science field, alternatively MSc and a minimum of 5 years of experience from industrial development/ R&D in the bioprocess area.
Experience working with purification of proteins and/or other biomolecules.
Experience of using ÄKTA chromatography systems.
English and Swedish as working languages.

It would be a plus if you also have:
Knowledge of methods used in analysis of biomolecules such as HPLC, Biacore, and/or Mass spectroscopy.
Experience from analytical method transfers from R&D to QC.

The ideal candidate is a result-oriented, flexible, and creative individual with a strong collaborative attitude. To succeed in this role, the ideal candidate should also be quality-focused, precise, and capable of working in a structured manner.
Interview and selection will happen continuously, and the opening can be filled before last day of application, September 15th. For questions regarding the role please contact hiring manager Johanna Tschöp, Senior Manager - Affinity Ligand Characterization, [email protected]. Welcome in with your application!
At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Research Engineer

Ansök    Aug 22    Cytiva Sweden AB    Analytisk kemist
Be part of something altogether life-changing Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly... Visa mer
Be part of something altogether life-changing
Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.
We are currently looking for a Research Engineer to the section for Analytical Technologies within the R&D Resins & Ligand Design department at Cytiva in Uppsala, Sweden. The mission of the Analytical Technology section is to support different departments within the company with expertise and technologies regarding analysis of resins, intermediates and other substances related to the production of the chromatographic process from start to finish. The team works closely with quality control and production units to support them with problem solving as well as method developments. In the role as Research Engineer, your focus will be on various analytical chemistry tasks, including method development and supporting in validation of analytical methods.
What you’ll do:
Be part of the team in several projects for new products and updates of the present products and perform analysis using different analytical methods.
Perform assignment analyses from the production and quality control departments.
Develop and optimize new analytical methods within the scope for the projects.
Support in validations.
Act as validation reviewer for various projects with respect to analytical methods.

The essential requirements of the job include:
MSc with a few years' of industrial experience within Analytical Chemistry.
Knowledge and expertise in adjacent areas of physical chemistry, such as chromotography, spectroscopy, titrations, microscopy, etc.
Fluency in both Swedish and English.

It would be a plus if you also possess previous experience in:
Validation of analytical methods.
Statistical analysis.
Previous experience working with Cytiva's products.

To be successful in this role, the ideal candidate should be a highly quality-oriented individual with an analytical mindset. In addition, we believe that the ideal candidate has a strong aptitude for identifying issues and developing creative and practical solutions, efficiently managing multiple tasks and meeting deadlines without compromising quality.
Interview and selection will happen continuously and the opening can be filled before last day of application. For questions regarding the role please contact hiring manager Gerd Rundström, Senior Manager Analytical Technologies, at [email protected].
At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

PLM Process & System Manager

Ansök    Aug 13    Cytiva Sweden AB    Systemansvarig
Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
At Cytiva, our vision is, to advance future therapeutics from discovery to delivery. Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The PLM (Product Lifecycle Management) team at Cytiva consists of five employees and contractors who work globally with development and maintenance of Cytiva’s Enovia based PLM system that is used for management of part/product and project data. The PLM system is the backbone in Cytiva for managing product related data and is integrated to enterprise systems such as Enterprise Resource Planning (ERP), Customer Relationship Management (CRM), Web and Sales Configurator.
The PLM Process & System Manager position is part of the PLM team located in Uppsala and will be an on-site role.
In this role, you will have the opportunity to:
Contribute to development of standardized PLM processes and associated system capabilities in Cytivas Enovia based PLM system to maximize productivity, whilst ensuring compliance, scalability/growth and alignment with overall business priorities
??Contribute to development of continuous improvement of engineering- and compliance processes and associated system capabilities through effective collaboration with business partners, by translating their needs into user requirements
??Work with Solution Architects and developers from IT to translate user requirements into system and user interface requirements
??Be accountable for User Acceptance testing and knowledge transfers to the Training Team for new/enhanced functionality in the PLM system
??Be responsible for third level end user support (expert level)

The essential requirements of the job include:
??Bachelor's degree in engineering or Life Sciences or equivalent business experience?
??Background from R&D/Engineering/Product Development?
??Interest and ability to work with cross-functional, multi-cultural teams and deliver results in an ambiguous- and dynamic environment?
??Process oriented and strong analytical skills with an interest to understand and interpret customer business needs and translate them into user and application requirements ?
??Experience from working with PLM-systems and managing product master data is an advantage?
??Experience from standardization, process- and systems improvements?
??Excellent written and verbal communication skills; fluent in English (oral and written)?
??Willing to travel domestically and internationally?

At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Senior Manager - QA Custom Hardware

Ansök    Aug 15    Cytiva Sweden AB    Kvalitetschef
Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The Senior Manager QA for Custom Engineering & SCO (Standard and Custom Operations) Sweden, independently leads, coordinates and prioritizes the work within the assigned site/s to ensure successful management of the QMS and associates processes.
The role is responsible for ensuring that the Custom Engineering Sweden team executes on deliveries, internal audits, QMS training, QMS documentation, complaints, NC/CAPA, product holds and field actions. Ensures compliance of the processes and drives a strong Quality Culture by engagement, empowerment, and inclusiveness.
This position is part of the QA Custom Hardware department located in Uppsala, Sweden and will be onsite. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
What you will do:
Be responsible for engaging strong intra departmental and cross-functional/organizational relationships to drive compliance and ensuring product quality
Be the QA representative in project steering committees as agreed with QA Director
Lead, coordinate, prioritize and follow-up the work within the team.
Engage, coach and develop the personnel.
Set goals for the team and follow up on completion.
Drive internal improvement work to assure continuous improvements.
Support key quality activities and be open to take on additional tasks supporting the overall performance of the QA Department

Who you are:
Bachelor’s degree preferably in a science or engineering discipline
A minimum of 5 years of experience in the Quality Assurance field
Experience of working as a manager within Quality Assurance/Quality Control
Comprehensive understanding of ISO 9001 requirements.
Experienced in continuous improvement methodologies & tools.
Experienced in leading external audits, including customer communications.
Excellent organizational, presentation, meeting facilitation and technical writing skills

It would be a plus if you also possess previous experience in:
Knowledge and awareness of the methods and techniques of Quality Control in the manufacturing industry.
Technical knowledge of systems/devices used in the biopharma field.
Fluency in Swedish both written and verbal communication

At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Custom Hardware Quotation Engineer

Be part of something altogether life-changing! Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that trul... Visa mer
Be part of something altogether life-changing!
Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.
The Custom Engineering department within Cytiva is responsible for delivering customized downstream hardware and software solutions used in Biopharma development and manufacturing. Each customer order becomes a project with dedicated resources from project management, design, manufacturing, sourcing, and verification teams. We are now looking for a Sales Support Engineer to further strengthen our global Hardware Quotation Support team (HQS).
What you’ll do:
Develop commercial and technical proposals which maximize profitability and add value for our customers.
Provide technical and product expertise of Bioprocess downstream hardware and automation solutions during pre-sales and quote phase.
Receive, analyze, and prioritize quote requests to ensure appropriate, and timely quote responses which satisfy customer expectations and meet user requirement specifications (URS).
Interpret customer specifications, drawings, and process application, and document any deviation from the URS.
Interface with sales, design teams, project management and other key personnel to gather information and evaluate technical feasibility.
Work closely with the project office and design organization to ensure smooth handover to project, design, and manufacturing for awarded customer orders.
Maintenance of your own quote portfolio and adherence to commercial, quality, and regulatory processes and systems.
Work with global colleagues across functions and teams to share best practices.
Occasional international travel is required to support commercial colleagues and customers.

The essential requirements of the job include:
MSc degree within Chemical, Electrical, Mechanical, Automation Engineering or equivalent educational background.
Several years of proven industry experience.
Demonstrated ability to comprehend and present complex material in a comprehensive way.
Experience working in a global, multi-cultural and team-oriented environment.
Strong coordination skills and capability to handle multiple parallel activities and projects.
Self-motivated, curious, and customer-focused.
Excellent communication skills with the ability to communicate professionally with both internal and external stakeholders.
Fluency in English, both oral and written, with excellent communication skills and ability to communicate professionally with both internal and external stakeholders.

It would be a plus if you also have:
Demonstrated knowledge of Bioprocessing and manufacturing of Biopharma products.
Product knowledge and technical expertise within the Bioprocess equipment area.
Familiarity with GMP and other relevant standards issued by FDA, ISO, etc.
Interest in, or experience with, UNICORN control system and/or distributed control systems such as Emerson DeltaV, Siemens or Rockwell are highly valued.

Interview and selection will happen continuously and the opening can be filled before last day of application. For any questions on the role, please contact hiring manager Sara Lidblad, Senior Manager Hardware Quotation Support, [email protected].
At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Product Manager, End of Life -Core R&T

Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
As The Product Manager, End of Life - Core R&T for Cytiva you will work alongside the CORE product management team to identify specific chromatography resins that are at, or transitioning from ‘mature’ to ‘End of Life’ product life cycle phase.
This position is part of the BioProcess Product Management Organization located in Uppsala and will be an on-site role. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
In this role, you will have the opportunity to:
Work alongside the CORE product management team to identify specific chromatography resins that are at, or transitioning from ‘mature’ to ‘End of Life’ product life cycle phase.
Take responsibility for this portfolio of materials, and where appropriate embark on the discontinuation process, based on a prioritization of such materials from discontinuation candidate identification, discontinuation process & project support through to ultimately discontinuing materials.
As responsible person for these materials you will apply the specific processes, operating mechanisms and ad hoc action such as:
Pricing process
Long term forecast
Product care initiatives, including raising business cases to support requests, engaging wider functions to increase traction to resolve issues.
On Time Delivery (OTD) improvements
Quality Response
Responding to incoming customer questions
In addition, across the wider CORE resins, you will own the responsibility to:
Identify and reduce Scrap and slow movers, following the standard process
And be front line support for:
Customer visit / audit support
Complaint case management
Impact assessment reviewer
As an integral member of the product management team, you will actively support and be supported by the product management team.

The essential requirements of the job include:
Bachelor’s degree in Life Sciences or Business
Business and customer-oriented with demonstrated ability to deliver results
Ability to understand and apply data to define actions and support decisions
Internal and external customer facing experience that demonstrates the capability to influence stakeholders
Fluency in English both written & oral communication

It would be a plus if you also possess previous experience in:
Previous experience within Product Management
The following systems: MAGIC, Qlik & SFDC

At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Senior PLM Process & System Manager

Ansök    Aug 13    Cytiva Sweden AB    Systemansvarig
Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
At Cytiva, our vision is, to advance future therapeutics from discovery to delivery. Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The PLM (Product Lifecycle Management) team at Cytiva consists of five employees and contractors who work globally with development and maintenance of Cytiva’s Enovia based PLM system that is used for management of part/product and project data. The PLM system is the backbone in Cytiva for managing product related data and is integrated to enterprise systems such as Enterprise Resource Planning (ERP), Customer Relationship Management (CRM), Web and Sales Configurator.
The Senior PLM Process & System Manager position is part of the PLM team located in Uppsala and will be an on-site role.
In this role, you will have the opportunity to:
Work with business stakeholders and functional teams to develop standardized PLM processes and associated system capabilities in Cytivas Enovia based PLM system to maximize productivity, whilst ensuring compliance, scalability/growth and alignment with overall business priorities
??Develop and drive continuous improvement of engineering- and compliance processes and associated system capabilities through effective collaboration with business partners, by translating their needs into user requirements
??Work with Solution Architects and developers from IT to translate user requirements into system and user interface requirements
??Be accountable for User Acceptance testing and knowledge transfers to the Training Team for new/enhanced functionality in the PLM system
??Be responsible for third level end user support (expert level)

The essential requirements of the job include:
??Bachelor's degree in engineering or Life Sciences or equivalent business experience?
??Solid background from R&D/Engineering/Product Development?
??Proven ability to work with cross-functional, multi-cultural teams and deliver results in an ambiguous- and dynamic environment?
??Process oriented and strong analytical skills, including a thorough understanding of how to interpret customer business needs and translate them into user and application requirements ?
??Experience from working with PLM-systems and managing product master data is an advantage?
??Experience from standardization, process- and systems improvements?
??Excellent written and verbal communication skills; fluent in English (oral and written)?
??Willing to travel domestically and internationally?

At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Processäkerhetsingenjör

Ansök    Aug 7    Cytiva Sweden AB    Säkerhetsingenjör
Bli en del av något helt livsavgörande Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier. På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbe... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier.
På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbeta med utmaningar som verkligen spelar roll tillsammans med människor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i 40 länder är Cytiva en plats där varje dag är en möjlighet att lära så att du kan få fart på din karriär och förbättra dina färdigheter på lång sikt.
Vi på Cytiva är stolta över att arbeta tillsammans med en grupp av nio andra Danaher Life Sciences-företag. Tillsammans är vi pionjärer inom vetenskap och medicin och utvecklar produkter som hjälper forskare i kampen att rädda liv.
Vi söker nu efter vår nästa processäkerhetsingenjör till avdelningen Environment, Health and Safety (EHS) på Cytivas anläggning i Uppsala. Som processäkerhetsingenjör hos oss ingår du i det lokala EHS-teamet bestående av ett 20-tal experter inom områdena processäkerhet, arbetsmiljö, yttre miljö och kemikaliehantering. Tillsammans verkar vi för en säker och hållbar arbetsplats med lägsta möjliga klimatavtryck. Har du ett intresse för processäkerhetsfrågor och vill bli del av ett tvärfunktionellt team med flera spännande kontaktytor på en Seveso-klassad produktionsanläggning? Då vill vi gärna höra från dig!
Som processäkerhetsingenjör hos oss ansvarar du för att säkerställa att processerna följer säkerhetsbestämmelser och standarder, identifiera och bedöma potentiella säkerhetsrisker, utveckla och implementera säkerhetsåtgärder, samt övervaka och rapportera om säkerhetsfrågor. Rollen innebär även att samarbeta med olika team för att förbättra säkerheten och att utbilda personalen i säkerhetsprocedurer.
Dina arbetsuppgifter:
Arbeta med riskhantering för processystem i syfte att förhindra olyckor som brand, explosion och okontrollerat utflöde från anläggningar som hanterar farliga ämnen.
Genomföra olika typer av riskanalyser så som Hazid, Hazop, SWIFT, grovriskanalys m.m.
Arbeta i ett team för processäkerhet med att utveckla och förbättra företagets rutiner som har processäkerhetspåverkan.
Delta i projektarbete med att definiera konstruktionskrav och följa upp dessa.
Vara en del i EHS teamets compliance kontroll, via lagbevakning och aktiviteter för att kontrollera lagefterlevnad på företaget.
Delta i Cytivas arbete för ständiga förbättringar, via till exempel hantering av händelserapporter, både lokalt och i globala sammanhang.
Föra dialog med externa aktörer, så som myndigheter och försäkringsbolag.
Utveckla instruktioner och hålla i utbildningar inom processäkerhetsområdet.

De huvudsakliga kraven för tjänsten är:
Lämplig utbildningsbakgrund är civilingenjörsexamen inom ett för tjänsten relevant område.
Ett par års erfarenhet av från kemisk/teknisk processindustri eller liknande.
Kunnig om säkerhetspraxis, analysmetoder och regelverk inom området.
Erfarenhet av riskhantering- och olycksutredningsmetodik.
Du kommunicerar obehindrat på såväl svenska som på engelska, både i tal och i skrift.

Det är även meriterande om du har tidigare erfarenhet av:
Utbildningsbakgrund med inriktning mot kemi eller kemiteknik.
Förtrogen med kravtolkning utifrån styrande lagar som tex Seveso, LBE, LSO och AML-lagstiftningen.

Vi ser gärna att du som söker är organiserad, arbetar med struktur och har en god förmåga att förankra och förklara dina beslut. Det är viktigt att du som person trivs i att coacha och ge stöd till verksamheten i processäkerhetsfrågor. Du arbetar självständigt, är initiativtagande och uppskattar samverkan med andra.
Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag, 15 september. För frågor rörande den här tjänsten vänligen kontakta rekryterande chef Sigrid de Geyter, EHS Director, på [email protected]. Varmt välkommen med din ansökan! Visa mindre

Additive Process Engineer

Be part of something altogether life-changing Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us –working on challenges that truly ... Visa mer
Be part of something altogether life-changing
Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us –working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity –so you can grow your career and expand your skills in the long term.
Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.
We are looking for an Additive Process Engineer to join our dynamic Additive Engineering team, which is part of the CTO organization, supporting all businesses and functions within Cytiva. The team is responsible for driving the scientific and technology agenda, providing additive manufacturing resources to New Product Development teams across Cytiva, and having a very strong relationship with Global Supply Chain to ensure continuity of product supply and supporting manufacturing improvement projects.
What you will do:
Development of new and existing Additive manufacturing processes with the goal to qualify new manufacturing lines, specifically in polymer printing.
Work closely with R&D teams in all business units across Cytiva, independently lead, perform and support process development for additive activities– from idea and concept development, via prototyping, to transfer to production.
Contribute with hands-on support in 3D printing and post-processing work – to understand how different material properties and production process are interconnected.
Take responsibility for ensuring rigor in determining processes requiring validation, development of plans and analysis criteria, execution and final analysis and acceptance.
Drive improved product quality by identifying manufacturing issues, developing advanced manufacturing cost-effective solutions, and overseeing successful implementation of Additive Manufacturing into production.

The essential requirements of the job include:
BSc/MSc in Material/Mechanical Engineering, or equivalent.
Experience working with Additive Manufacturing (3D printing).
A few years experience in product/process development.
Fluent in English – both written and verbal.

It would be a plus if you also have:
Deep understanding of material science in polymer.
Experience from working with validation processes in a manufacturing environment.
Fluent in Swedish – both written and verbal.

To be successful in this role, we believe that you are a creative and focused on customer-focused individual with excellent interpersonal and communication skills. In addition we're looking for someone who's enjoys problem-solving and troubleshooting, with the ability to work effectively both independently and with others.
This position is based at our site in Uppsala, Sweden and is a full-time position.
This position will remain posted over the holiday season (June-July), and we expect to initiate selection of candidates early August. For questions regarding the role please contact David Bergman, Additive Engineering Manager, [email protected].
At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

System Engineer

Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The System Engineer for Cytiva plays a crucial role in defining, developing, and implementing hardware and software solutions for our large-scale bioprocess systems. You will work closely with cross-functional teams to ensure the successful integration and functionality of our cutting-edge bioprocess equipment.
You will have the opportunity to work with world-leading products in Life Sciences and work daily with fantastically talented and committed colleagues. You will be involved in the entire product life cycle from development to maintenance and support with focus on single-use products.
This position is part of the ÄKTA Instrument Engineering in R&D located in Uppsala and will be an on-site role. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
In this role, you will have the opportunity to:
Deliver new single-use products to the market and our bioprocess customers.
Collaborate with cross-functional teams, including mechanical engineers, electrical engineers, and software developers, to ensure seamless integration and performance of the bioprocessing systems.
Contribute with product and customer expertise across the organization
Understand the need from the customer and define system requirements.
Develop and execute test plans to verify and validate hardware functionality, ensuring compliance with industry standards and regulations.
Support the manufacturing and assembly processes, working closely with production teams to ensure efficient and reliable manufacturing of hardware components.
Stay up to date with the latest advancements in hardware technology relevant to the bioprocess industry and propose innovative solutions to improve system performance and efficiency.
Provide technical expertise and guidance to junior engineers and cross-functional team members.

The essential requirements of the job include:
Master’s degree in biotechnology, Chemical Engineering or a related field.
Experience of system and/or software specification, verification and validation.
Experience with ÄKTA chromatography systems and UNICORN software
Knowledge & experience from new product development
Hands-on experience in protein purification, including familiarity with process design and scale-up for chromatography operations
Good understanding of GxP policies and procedures; basic knowledge of regulatory requirements of the pharmaceutical and/or biotechnology industry.
Demonstrated ability to deliver according to deadlines
Experience from work in multidisciplinary environments
Strong communication and interpersonal skills, with the ability to effectively communicate technical concepts to both technical and non-technical stakeholders.

At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Technical Writer

Be part of something altogether life-changing Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly... Visa mer
Be part of something altogether life-changing
Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.
The Technical Writer for Cytiva is responsible for producing and maintaining customer-facing user documentation, in a manner that meets corporate standards and style, for products developed and maintained at Cytiva. This position is part of the Technical Documentation group (TechDoc) located in Uppsala and will be a hybrid role. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
What you’ll do:
Research, write, edit, review, proof-read, and publish end-user documentation to ensure completeness, accuracy, validity, and clarity of information for digital and/or print production in line with corporate standards for style and quality.
Work with Product Management, R&D and PMO to ensure the timely and cost-effective production of new documents and maintenance of existing documents.
Fulfil end-user documentation assignments such as production of new technical documentation for new or customized product introductions, or updates of existing technical documentation.
Estimate and schedule the time required to complete assignments and provide regular updates of progress.
Update appropriate databases and inform appropriate functions of the availability of new and revised documents.
Assist in the definition of development tools and platforms for efficient production and maintenance of end-user documentation and instructions.

The essential requirements of the job include:
MSc degree preferably in biology chemistry, molecular biology, or related field; or BSc Science preferably in biology chemistry, molecular biology, or related field with minimum 2 years of relevant work experience.
1+ years of progressively responsible experience in the writing, editing, and production of technical documentation (e.g., user manuals) in a life science or similar setting.
1+ years of progressively responsible experience in the creation of illustrations and graphics for the production of technical documentation (e.g., user
manuals) in a life science or similar setting.
Excellent written and verbal communication skills; demonstrated ability in original technical writing, document organization, document reorganization; experience editing others’ work.
Knowledge of the Cytiva products.
Experience of SDL Tridion or other XML based Content Management Systems.
Proficiency in desktop publishing tools, for example Adobe InDesign, Photoshop and Illustrator.
Fluent in English.

It would be a plus if you also possess previous experience in:
Strong communication, interpersonal, analytical, and problem-solving skills
Excellent organizational skills and attention to detail.
Ability to work on multiple parallel projects, to work independently and as part of a team, to work under time pressures and meet deadlines, to work with marketing, product management, and scientific staff.
Demonstrated ability to take initiative, pursue tasks to completion, results oriented.
Experience of CAD related tools.

At Cytiva we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, hybrid working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a hybrid work arrangement in which you can work part-time at the Company location identified above and part-time remotely from your home. Additional information about this hybrid work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide.
Interview and selection will happen continuously and the opening can be filled before last day of application. For questions regarding the role please contact hiring manager Gail Adam at [email protected].
At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Senior Technical Writer

Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The Senior Technical Writer for Cytiva is responsible for producing and maintaining customer-facing user documentation, in a manner that meets corporate standards and style, for products developed and maintained at Cytiva.
This position is part of the Technical Documentation group (TechDoc) located in Uppsala and will be a hybrid role. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
In this role, you will have the opportunity to:
Fulfil end-user documentation assignments such as production of new technical documentation for new product development (NPD) or updates of existing technical documentation. Estimate and schedule the time required to complete assignments and provide regular updates of progress.
Write, edit, review, proof-read, approve, process translations, and publish end-user documentation to ensure completeness, accuracy, validity, and clarity of information for digital and/or print production in line with corporate standards for style, branding and quality, legal guidelines, and regulatory requirements.
Work with other functions (such as product management, research & development, regulatory, manufacturing, and project management) for the timely and cost-effective production of new documents and maintenance of existing documents.
Coordinate writer activities for larger projects involving multiple deliverables and report status to stakeholders.
Act as mentor for Technical Writers. Provide guidance to Technical Writers on strategic decisions regarding content, design, documentation strategy, tools etc. Be the escalation path for project concerns for Technical Writers.
Knowledge sharing, contribute with technical writing, ways of working, organization and product area expertise to the team.
Define instructions and processes. Assist in defining and implementing new tools and platforms for efficient production and maintenance of user documentation. Drive continuous improvements.

The essential requirements of the job include:
MSc degree preferably in biology chemistry, molecular biology, or related field; or BSc Science preferably in biology chemistry, molecular biology, or related field with a minimum of 4 years of relevant work experience.
Several years of progressively responsible experience in the technical writing, editing, and production of user documentation, preferably in a life science or medical device setting.
Excellent English skills, good knowledge of Technical English and Information Mapping.
Excellent written and verbal communication skills; demonstrated ability in original technical writing, document organization, document reorganization; experience editing others’ work.
Experience working with cross-functional teams and stakeholders.
Knowledge of Cytiva products, in particular with consumables (e.g. resins, single use, cell culture media, ELISA kit, filters, columns), medical devices and/or cell therapy products.
Experience in working in Content Management Systems such of SDL Tridion or other XML based systems and with publishing tools such as Adobe InDesign, Photoshop and Illustrator.

It would be a plus if you also possess previous experience in:
Excellent organizational skills, strong communication and interpersonal skills.
Process and detail-oriented, ability to prioritize and take initiative.
Demonstrated ability to pursue tasks to completion, work on multiple projects in parallel, results oriented, problem-solver and self-motivated.

At Cytiva we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, hybrid working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a hybrid work arrangement in which you can work part-time at the Company location identified above and part-time remotely from your home. Additional information about this hybrid work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide.
Interview and selection will happen continuously and the opening can be filled before last day of application. For questions regarding the role please contact hiring manager Barbara Yermen at [email protected].
#LI-HJ2
At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Technical Writer

Be part of something altogether life-changing! Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that trul... Visa mer
Be part of something altogether life-changing!
Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.
The Technical Writer for Cytiva is responsible for producing and maintaining customer-facing user documentation, in a manner that meets corporate standards and style, for products developed and maintained at Cytiva. This position is part of the Technical Documentation group (TechDoc) located in Uppsala and will be a hybrid role. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
What you’ll do:
Research, write, edit, review, proof-read, and publish end-user documentation to ensure completeness, accuracy, validity, and clarity of information for digital and/or print production in line with corporate standards for style and quality.
Work with Product Management, R&D and PMO to ensure the timely and cost-effective production of new documents and maintenance of existing documents.
Fulfil end-user documentation assignments such as production of new technical documentation for new or customized product introductions, or updates of existing technical documentation.
Estimate and schedule the time required to complete assignments and provide regular updates of progress.
Update appropriate databases and inform appropriate functions of the availability of new and revised documents.
Assist in the definition of development tools and platforms for efficient production and maintenance of end-user documentation and instructions.

The essential requirements of the job include:
MSc degree preferably in biology chemistry, molecular biology, or related field; or BSc Science preferably in biology chemistry, molecular biology, or related field with minimum 2 years of relevant work experience.
1+ years of progressively responsible experience in the writing, editing, and production of technical documentation (e.g., user manuals) in a life science or similar setting.
1+ years of progressively responsible experience in the creation of illustrations and graphics for the production of technical documentation (e.g., user
manuals) in a life science or similar setting.
Excellent written and verbal communication skills; demonstrated ability in original technical writing, document organization, document reorganization; experience editing others’ work.
Knowledge of the Cytiva products.
Experience of SDL Tridion or other XML based Content Management Systems.
Proficiency in desktop publishing tools, for example Adobe InDesign, Photoshop and Illustrator.
Fluent in English.

It would be a plus if you also possess previous experience in:
Strong communication, interpersonal, analytical, and problem-solving skills
Excellent organizational skills and attention to detail.
Ability to work on multiple parallel projects, to work independently and as part of a team, to work under time pressures and meet deadlines, to work with marketing, product management, and scientific staff.
Demonstrated ability to take initiative, pursue tasks to completion, results oriented.
Experience of CAD related tools.

At Cytiva we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, hybrid working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a hybrid work arrangement in which you can work part-time at the Company location identified above and part-time remotely from your home. Additional information about this hybrid work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide.
Interview and selection will happen continuously and the opening can be filled before last day of application. For questions regarding the role please contact hiring manager Gail Adam at [email protected].
#LI-HJ2
At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Senior Technical Writer

Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care... Visa mer
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The Senior Technical Writer for Cytiva is responsible for producing and maintaining customer-facing user documentation, in a manner that meets corporate standards and style, for products developed and maintained at Cytiva. This position is part of the Technical Documentation group (TechDoc) located in Uppsala and will be a hybrid role. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
In this role, you will have the opportunity to:
Fulfil end-user documentation assignments such as production of new technical documentation for new product development (NPD) or updates of existing technical documentation. Estimate and schedule the time required to complete assignments and provide regular updates of progress.
Write, edit, review, proof-read, approve, process translations, and publish end-user documentation to ensure completeness, accuracy, validity, and clarity of information for digital and/or print production in line with corporate standards for style, branding and quality, legal guidelines, and regulatory requirements.
Work with other functions (such as product management, research & development, regulatory, manufacturing, and project management) for the timely and cost-effective production of new documents and maintenance of existing documents.
Coordinate writer activities for larger projects involving multiple deliverables and report status to stakeholders.
Act as mentor for Technical Writers. Provide guidance to Technical Writers on strategic decisions regarding content, design, documentation strategy, tools etc. Be the escalation path for project concerns for Technical Writers.
Knowledge sharing, contribute with technical writing, ways of working, organization and product area expertise to the team.
Define instructions and processes. Assist in defining and implementing new tools and platforms for efficient production and maintenance of user documentation. Drive continuous improvements.

The essential requirements of the job include:
MSc degree preferably in biology chemistry, molecular biology, or related field; or BSc Science preferably in biology chemistry, molecular biology, or related field with a minimum of 4 years of relevant work experience.
Several years of progressively responsible experience in the technical writing, editing, and production of user documentation, preferably in a life science or medical device setting.
Excellent English skills, good knowledge of Technical English and Information Mapping.
Excellent written and verbal communication skills; demonstrated ability in original technical writing, document organization, document reorganization; experience editing others’ work.
Experience working with cross-functional teams and stakeholders.
Knowledge of Cytiva products, in particular with consumables (e.g. resins, single use, cell culture media, ELISA kit, filters, columns), medical devices and/or cell therapy products.
Experience in working in Content Management Systems such of SDL Tridion or other XML based systems and with publishing tools such as Adobe InDesign, Photoshop and Illustrator.

It would be a plus if you also possess previous experience in:
Excellent organizational skills, strong communication and interpersonal skills.
Process and detail-oriented, ability to prioritize and take initiative.
Demonstrated ability to pursue tasks to completion, work on multiple projects in parallel, results oriented, problem-solver and self-motivated.

At Cytiva we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, hybrid working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a hybrid work arrangement in which you can work part-time at the Company location identified above and part-time remotely from your home. Additional information about this hybrid work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide.
Interview and selection will happen continuously and the opening can be filled before last day of application. For questions regarding the role please contact hiring manager Gail Adam at [email protected].
#LI-HJ2
At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Senior Regulatory Support Manager

Be part of something altogether life-changing Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care ... Visa mer
Be part of something altogether life-changing
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
We’re looking for a Senior Regulatory Support Manager to join Cytiva’s Customer Regulatory Support (CRS) team at our facilities in Uppsala. As Senior Regulatory Support Manager, you are responsible for providing support to Product Managers, Regions and customers by providing quality documents and regulatory support in response to customers’ requests for quality, regulatory and technical-related information. As a member of the Customer Regulatory Support team, you will add value to BioProcess products and demonstrate a commitment to customer satisfaction.
What you’ll do:
Lead area team within CRS or over-arching product/area activities and critical projects.
Build and maintain knowledge and understanding of customers’ regulatory requirements related to the BioProcess business at a high level, specifically regarding product area chromatography resin.
Ensure availability of right Regulatory Support documentation for customers in regulated environment.
Participate/drive in creating and updating guidelines and steering documents.
Act as regulatory support expert in projects and discussion partner to R&D, QA, Product Management and other functions and regions.
Respond efficiently and promptly to customers’ regulatory based issues, which will include necessary investigations, preparations and delivery of certificates, use of available internal and external databases and other relevant databases.
File and maintain complete documentation of questions and answers in databases; specify, prepare, update and review regulatory support documentation, including RSF, VG, VSF, CCN, statements, certificates and other regulatory related documentation for new and existing products.

The essential requirements of the job include:
Bachelor of Science in Chemistry, Biotechnology, Pharmacy or equivalent educational background.
At least 8 years’ of experience from relevant positions within Quality Assurance, Regulatory, or Product Management.
Excellent communication skills and fluency in English, both written and spoken.
Deep understanding of GMP and knowledge of regulatory requirements in Pharmaceutical, Biotechnology, Medical Device, or Life Science industry.

It would be a plus if you also have:
Experience leading cross-functional activities in large matrix organizations.
Fluency in the language of the country of employment.
Experience in customer communication.

Interview and selection will happen continuously and the opening can be filled before last day of application. For questions regarding the role please contact hiring manager Henrik Norberg [email protected]. We look forward to hearing from you!
At Cytiva we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, hybrid working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a hybrid work arrangement in which you can work part-time at the Company location identified above and part-time remotely from your home. Additional information about this hybrid work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide.
#LI-HJ2
At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Produktionsingenjör

Bli en del av något helt livsavgörande Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier. På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbe... Visa mer
Bli en del av något helt livsavgörande
Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier.
På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbeta med utmaningar som verkligen spelar roll tillsammans med människor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i 40 länder är Cytiva en plats där varje dag är en möjlighet att lära så att du kan få fart på din karriär och förbättra dina färdigheter på lång sikt.
Vi på Cytiva är stolta över att arbeta tillsammans med en grupp av nio andra Danaher Life Sciences-företag. Tillsammans är vi pionjärer inom vetenskap och medicin och utvecklar produkter som hjälper forskare i kampen att rädda liv.
Vill du vara del av ett starkt team där du kan påverka din vardag på jobbet? Vill du ha ett varierande arbete där du får arbeta praktiskt men även utvecklas med teknologiska lösningar? Är du en engagerad och nyfiken person som letar efter nästa utmaning? Då kan du vara den nya medarbetare som vi söker!
Arbetsuppgifter
Vi söker en Produktionsingenjör till sektionen Kolonnproduktion och är en del av den kemiska produktionen på vår site i Uppsala. Gruppen består av både operatörer och ingenjörer som tillsammans tillverkar kromatografikolonner i labskala på 15 olika produktionslinor. Kolonnproduktionen är en del av den kemiska produktionen inom Cytiva. Rollen som produktionsingenjör på Cytiva innebär framför allt att du är ett dagligt stöd till produktionen. Rent praktiskt kan det innebära att du arbetar med att:
Driva Change Control-ärenden och avvikelsehantering.
Teknisk felsökning av processutrustning.
Kontakt med underhållsavdelning och/eller entreprenörer.
Samarbeta med F&U vid nyproduktprojekt och produktvårdsprojekt.
Agera som stöd i reklamationsärenden och driva utredningar rörade reklamationer.

Du driver även förbättringsarbete, uppdaterar produktionsdokument samt utför och dokumenterar riskanalyser mm. Ingenjörsarbetet präglas av variation och en möjlighet till att påverka den dagliga verksamheten, där tillverkningen står i fokus.
De huvudsakliga kraven för tjänsten är:
Civilingenjör eller motsvarande med inriktning mot bioteknik/kemiteknik/maskinteknik eller liknande utbildningsbakgrund.
Du behärskar svenska och engelska flytande i tal och skrift.
God datorvana och trygg användare av olika IT-system.

Det är även meriterande om du har tidigare erfarenhet av:
Goda kunskaper om process- och produktutveckling.
Erfarenhet av att beräkna och optimera kapacitet samt resursbehov och förbrukning, i olika typer av produktionsavsnitt.
Tidigare erfarenhet av kolonnpackning.

För att vara framgångsrik i denna roll ser vi gärna att du är en lagspelare med god samarbetsförmåga och att du trivs i med att jobba både med teknik och med människor. Vidare ser vi gärna att du är en säkerhets- och kvalitetsmedveten person med god förmåga att ta initiativ och driva flera parallella aktiviteter samtidigt.
Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. För frågor rörande den här tjänsten vänligen kontakta rekryterande chef Martina Brolin [email protected]. Varmt välkommen med din ansökan! Visa mindre