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CAPA Leader

Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing innova... Visa mer
Help us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.
What You'll Do
In this role you will be the CAPA leader for the Uppsala Site. As the CAPA process owner you will ensure that the process is effective and continuously improved by monitoring performance. You will coach individuals in how to work as well as hold trainings in the CAPA process and how to use our IT tool. You will lead the Site CAPA board with cross functional management representation, presenting appropriate data and metrics showing performance and drive needed actions and decisions.
You will also as part of the Site QA Team support key quality activities be open to take on additional tasks supporting the performance of the team by for ex perform internal audits, and/or lead an improvement project (locally and globally) and/or coach more junior QA engineers.
For questions related to this opening, please contact Hiring Manager Christine Wahlgren ([email protected]).
Who you are
You have experience in working with quality assurance, solid experience of working with the CAPA process, and you can communicate effectively (both written and oral) in Swedish and English.
You can work independently in a changing environment with minimal supervision. Quality focused, attentive to detail and results oriented. You have problem solving skills. You have ability to influence positive change effectively and you energize and motivate others by building a connection with team´s /people through personal involvement, trust and by providing feedback.
Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.
Want to know more? Take a look at our Careers website, Instagram och LinkedIn page!
Cytiva is a 3.5 billion USD global life sciences leader with over 7000 associates across 40 countries who are dedicated to our mission to help us improve access to life-changing therapies that transform human health. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients.
As part of the Danaher family of companies, our work at Cytiva is supported by a global science and technology innovator. In addition to Danaher’s unrivaled leadership training and professional development programs, our relationship also provides expanded career opportunities across industries and brands. Together, we are united by a shared purpose: Helping Realize Life’s Potential.
Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here.
Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here. Visa mindre

GSC Strategy Leader - Hardware

Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing innova... Visa mer
Help us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.
The Strategy leader position is accountable for leading the transformation of global supply chain operations through development and execution of wing to wing supply chain capability & capacity planning, localization, simplification and variable/base cost productivity projects. This role supports Biopharma hardware supply chain functional and all Product/Franchise P&L leadership teams on matters of product cost, product quality, fulfillment, EHS, sourcing / manufacturing / logistic strategy, and supply chain and business operating performance.
What you’ll do
Elaborate & Align BP GSC Strategic Roadmap with customer priorities, Policy Deployment (Hoshin Kanri) in collaboration with each Product Segment & Regional P&L
Define, Prioritize & Launch cross functional GSC strategic projects to improve capacity, leadtime and cost i.e Make/Buy, Make Where, High Level Assembly, Automation, Additive printing, transfer/localization manufacturing/warehousing strategy projects including planning, capex/opex funding, team structure, resourcing and risk mitigation.
Leverage the Operations Excellence functional teams (Technical Operations, Lean, 6 sigma, System & Process) to prioritize & optimize CAPEX, Opex, Competency gaps & resource allocation
Collect & Provide GSC design input to the Product Design team to standardize the product offering through sales configurator tool
Define & Plan BP GSC Wing to Wing Security of Supply strategy including dual source, dual make, Enterprise Resource Planning, In Region for Region…through early supply chain engagement in NPI and Life Cycle management.
Measure Strategic Project impact on customer through regular Say/do & lessons learnt sharing sessions
Support Business Development functional team for due diligences, acquisition, partnership, strategic alliances
Participate to the planning & execution strategy for new Business Integrations

Who you are
Master Degree in Engineering, Manufacturing or other relevant technical discipline and 10 years experience with proven leadership in manufacturing, supply chain or R&D role
Strong communication Skills, written and verbal.
Proven mentoring and coaching abilities, demonstrated ability to motivate & inspire others
Demonstrated leadership, energizing teams and project management
Ability to successfully motivate and maintain high moral, employee involvement, safety and teamwork in an union environment
Demonstrated ability to deliver results in an ambiguous environment
Proven leadership skills (experience successfully managing people/projects/issues)
Change agent with energy, passion & enthusiasm to drive change
Demonstrated effective interpersonal, teamwork & networking skills
Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position
Solid working knowledge of Cytiva Phase Review Discipline procedures
Working knowledge of Lean tools and Lean thinking.
Six Sigma trained with demonstrated ability to apply tools and process rigor
Willing to travel internationally and domestically up to 25% of the time

For any questions in regards to this opening, please contact hiring manager David Morel ([email protected]).
Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.
Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page!
Cytiva is a 3.3 billion USD global life sciences leader with nearly 7000 associates across 40 countries who are dedicated to our mission to advance and accelerate therapeutics. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients.
Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world.
Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here.
Apply Now Visa mindre

European Patent Attorney, Life Sciences

Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing innova... Visa mer
Help us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.
We are looking for a European Patent Attorney to work with our expert Intellectual Property team of fifteen employees across the world. The position will have a particular focus on building and implementing the IP strategy for protecting one of Cytiva’s core product portfolios relating to chromatography resins and protein ligands for Bioprocess applications. This will cover all aspects from collaborating closely with IP, R&D and business colleagues to build a world class IP portfolio, through to, where necessary, patent enforcement.
Do you have a passion for innovation and intellectual property? Then we would love to hear from you.
What you’ll do
Work closely with R&D and product development teams to capture and protect commercially significant inventions.
Draft and file high quality patent applications.
Efficiently advance prosecution of pending patent applications, and manage global patent portfolio to ensure that meaningful protection is obtained.
Act as the European representative before the European Patent Office for European patent applications.
Develop IP strategies using various types of IP to create and nurture valuable IP assets.
Perform freedom to operate reviews and minimize exposure to third party IP.
Support IP aspects of business development, licensing, and M&A activities.
Represent Cytiva in EPO opposition proceedings.
IP litigation support.
Provide IP training to R&D, product and marketing teams.

Who you are
Qualified European Patent Attorney.
Technical background in biology, biochemistry, chemistry or related life sciences field.
Excellent written and oral communication skills.
Experience of devising innovative IP strategies.
Good commercial awareness.
Experience working in the life sciences or healthcare sector.
Whilst expertise to advise on IP matters in the biology/chemistry fields is essential, experience and desire to work additionally in product areas pertaining to other technical fields would be desirable.
Knowledge of laws, regulations, practices and procedures relating to patent procurement in Europe, US and Asia.

Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.
Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page!
Cytiva is a 3.5 billion USD global life sciences leader with over 7000 associates across 40 countries who are dedicated to our mission to help us improve access to life-changing therapies that transform human health. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients.
Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world.
Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here. Visa mindre

Processoperatör Uppsala

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. Som tidigare del av GE Healthcare har vi ett rikt arv av värdefull erfarenhet och en nystart sedan 2020. Våra kunder bedriver livsavgörande forskning och produktion, alltifrån biologisk forskning till utveckling av nya vaccin... 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. Som tidigare del av GE Healthcare har vi ett rikt arv av värdefull erfarenhet och en nystart sedan 2020.
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.
Dina arbetsuppgifter
Du kommer jobba i sektionen Fyllning & Förpackning. I sektionen fyller vi gelkromatografimedia, förpackar kit, tillverkar och fyller celldensitetsmedia, tillverkar buffertar och elektroforesgeler. Fokus för dig kommer att vara tillverkning av elektroforesgeler; det innebär att du kommer bereda lösningar, gjuta geler samt förpacka dessa. Vi jobbar efter fastställda metoder och batchprotokoll. I de flesta fall utför vi sista steget ut mot kund, så det är viktigt att du är noggrann och servicebenägen. Arbetet är till stor del manuellt och du kommer jobba med kemikalier.
Utöver tillverkningen tillkommer administrativa uppgifter så som material- och tidsavbokningar, beställning av material, planering och arbete med ständiga förbättringar. Du får även vara med i projekt som drivs och felsöka om eventuella problem uppstår.
Vem är du
Du är noggrann, flexibel och kvalitetsmedveten.
Du har en postiv grundinställning och kommer gärna med egna intiativ och förbättringsförslag.
Du tycker om att jobba i en liten grupp och ser utmaningar istället för problem.
Du har tidigare jobbat inom tillverkning och då med inriktning mot kemisk tillverkning, eller laborativt arbete.
Önskvärd utbildning är tex något av följande gymnasieutbildning inom naturvetenskap/teknik, högskoleingenjör, KY-utbildning processoperatör.
Vilka är vi?
Oavsett din roll, ger vi dig ett syfte och en utmaning varje arbetsdag. Om du drivs av att göra världen till en bättre plats genom vetenskap och medicin, kommer du att känna dig hemma här. Är du flexibel, nyfiken och envis är du rätt person. Trivs du dessutom i en global kultur, kan detta vara platsen för din fortsatta karriär.
För frågor rörande tjänsten kontakta Helena Rubbetoft, [email protected], 018-6120639
Vill du veta mer? Spana in vår Careers webbsida, Instagram-kanal och LinkedIn-sida!
Cytiva är en 3,3 miljarder USD global ledare inom biovetenskap med nästan 7 000 anställda i 40 länder som är hängivna vårt uppdrag att främja och påskynda behandlingar. Som en pålitlig partner till kunder världen över bidrar Cytiva till ett effektivt arbetsflöde till forskning och utveckling, säkerställer tillverkning och leverans av omvälvande mediciner till patienter.
Cytiva är en del av Danaher-familjen, en global nyskapare inom vetenskap och teknologi som är hängiven att hjälpa kunder att lösa komplexa utmaningar samt förbättra livskvaliteten välden över.
Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here. Visa mindre

IT Infrastructure Engineer Server / Storage

Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing innova... Visa mer
Help us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services -the pots, pans, soups and sauces -they need to work better, faster and safer, leading to better patient outcomes.
We are looking for a Senior IT Infrastructure Engineerto work with our expertin IT team of +200 employees across the world. Do you have a passion for IT Infrastructure ? Then we would love to hear from you.
What you’ll do
•Build and manage local IT infrastructure, servers, storage and backups
•Lead small project initiatives both on local level and global level within IT Infrastructure area
•Understand business needs and map them into right IT solutions
•Effectively uncover, align and manage stakeholders needs and expectations
•Work closely with the teams for delivery and operation to support quality in delivery of solutions and continuous excellence of support of solutions
For questions related to this opening, please contact Hiring Manager Björn Olsson ([email protected]).
Who you are
•Minimum of 8 years of experience
•Expertise with vCenter and other VMWare hypervisor
•Expertise in storage solutions like NAS, SAN
•Expertise in Active Directory, domain policies and VDIsolutions
•Strong collaborationand communication skills
•Expertise in ITIL Foundation
•Proficient at operating within a globally distributed team
Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.
Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page!
Cytiva is a 3.5 billion USD global life sciences leader with over 7000 associates across 40 countries who are dedicated to our mission to help us improve access to life-changing therapies that transform human health. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients. Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world.
Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here. Visa mindre

EMEA SERVICE QA LEADER

Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing inno... Visa mer
Help us improve access to life-changing therapies that can transform human health


We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.
We are looking for a EMEA SERVICE QA LEADER to work with our expert Services team of 800 employees across the world.


What you’ll do
This position is responsible for leading QA support & compliance activities for EMEA region for Global services, reporting to global Service QA Director. He/she represents Cytiva to external agencies and champions the evolution of the quality culture for the function which includes executing and driving site quality objectives, metrics, reporting and operating mechanisms. This role is also responsible for completing and maintaining oversight of both supplier and customer related activities including but not limited to document control, compliance training, SCAR management, customer interactions, complaints and CAPA management.
Drive on-time closure of customer feedback, Investigation and CAPA etc. through regular business touch points, such as CHU, CAPA Board, Ops Review & Quality Council etc. As well as supporting internal external audit and QMR.
Lead process standardization and improvement with Service teams, such as Qualification Service, Customer Bioprocess Service, Goldseal, Global Service Engineering and repair depot etc.
Responsible for leading the development of changes to the Services quality management system in line with business strategic priorities. Educate & drive implementation of new QMS requirements/priorities from business or corporate. Drive a continuous improvement culture based on data trends and promote customer satisfaction culture
Influences product compliance, process development and new product introduction (NPI) including automation software. Support ad-hoc assignment based on business needs, including domestic and/or international travel request.

Preferred location for this opening are our Swedish locations in Uppsala or Umeå. Cardiff and Amersham in the UK are optional locations.


Who you are


Relevant university degree in combination with at least 5 years of QA working experience
Hands-on experience with FDA, QSR, ISO(ISO9001/ISO13485), MDD and /or other international quality systems requirements, plus audit experience
Strong presentation skill and data analysis skill using word processing, spreadsheet, and other data analyzing tools.
Ability to multi-task & handle tasks with competing priorities effectively, as well as exercising collaboration, negotiation & conflict resolution skills
Proven mentoring and coaching abilities to motivate & inspire others by effective interpersonal, teamwork & networking skills
Fluency in English as well as valid work permission



Desired experience:


Demonstrated validation experience in pharmaceutical or medical device industry.
Understanding of product development, manufacturing, quality control and servicing in a pharmaceutical or medical device environment preferred
Digital QMS experience would be an advantage.



Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.
Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page!
Cytiva is a 3.3 billion USD global life sciences leader with nearly 7000 associates across 40 countries who are dedicated to our mission to advance and accelerate therapeutics. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients.
Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world.
Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here. Visa mindre

Processoperatör Proteins

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. Som tidigare del av GE Healthcare har vi ett rikt arv av värdefull erfarenhet och en nystart sedan 2020. Våra kunder bedriver livsavgörande forskning och produktion, alltifrån biologisk forskning till utveckling av nya vacci... 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. Som tidigare del av GE Healthcare har vi ett rikt arv av värdefull erfarenhet och en nystart sedan 2020.
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 drivna processoperatörer till Proteinsektionen inom Produktion Uppsala. Sektionen kommer under året gå över till 7-dagars schema vilket innebär arbete var 4:e helg. Sektionen ansvarar för odling och rening av proteinligander. Har du en passion för bioteknik? Då vill vi gärna höra ifrån dig.

Dina arbetsuppgifter
Vara del av den dagliga produktionen
Delta i expansionen av produktionsavsnittet proteintillverkning
Driva förbättringsarbete (LEAN)
Kalibrera utrustning enligt metod
Medverka i förbättringsarbetet av processer och utrustning

Vänligen kontakta rekryterande chefen Göran Bauren ([email protected]) för frågor kring denna öppningen. Sista ansökningsdag är den 21 juni. Intervjuer sker löpande.

Vem är du
Vi söker dig som har gymnasieutbildning med inriktning mot kemi, processteknik eller liknande
Erfarenhet av processindustri, gärna inom kemisk produktion och/eller läkemedelsproduktion med erfarenhet av att arbeta med styrsystem.
Goda kunskaper i svenska och engelska
Du bör ha ett gediget tekniskt intresse och drivas av att lära dig nya processer.
Du är noggrann och har gott ordningssinne
Som person bör du vara ambitös, driftig och initiativtagande med god kommunikationsförmåga
Du bör ha god datorvana och gärna erfarenhet av outlook, word, excel och Oracle.

Vilka är vi?
Oavsett din roll, ger vi dig ett syfte och en utmaning varje arbetsdag. Om du drivs av att göra världen till en bättre plats genom vetenskap och medicin, kommer du att känna dig hemma här. Är du flexibel, nyfiken och envis är du rätt person. Trivs du dessutom i en global kultur, kan detta vara platsen för din fortsatta karriär.

Vill du veta mer? Spana in vår Careers webbsida, Instagram-kanal och LinkedIn-sida!
Cytiva är en 3,3 miljarder USD global ledare inom biovetenskap med nästan 7 000 anställda i 40 länder som är hängivna vårt uppdrag att främja och påskynda behandlingar. Som en pålitlig partner till kunder världen över bidrar Cytiva till ett effektivt arbetsflöde till forskning och utveckling, säkerställer tillverkning och leverans av omvälvande mediciner till patienter.

Cytiva är en del av Danaher-familjen, en global nyskapare inom vetenskap och teknologi som är hängiven att hjälpa kunder att lösa komplexa utmaningar samt förbättra livskvaliteten välden över.

Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here. Visa mindre

Data Scientist / Lead Black Belt

Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing in... Visa mer
Help us improve access to life-changing therapies that can transform human health


We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.


Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.


What You'll Do
You will, as part of R&D, contribute to the development of new products which are used in the manufacturing of leading biological drugs. Your tasks will include work all the way from idea generation, research and development work and finally transfer to production scale. You will also take active part in trouble shooting of existing Cytiva and customer processes. The Uppsala Cytiva site is a workplace for more than 1200 persons 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.
More specifically will your tasks include:
- Drive and foster a data driven culture including Six Sigma processes and tools within RnD
- Leadership in value-creation from smart data management
- Perform data analysis in development project and trouble-shooting activities
- Setting up structured experimental plans
- Identify, implement new techniques and follow the technical development in the field
- Independently plan and accomplish given tasks, to reach given project objectives
- Independently solve problems of “trouble shooting character” in project work
- Document and report results both orally and written


Who you are
- Master degree in engineering or technical discipline with expert competency in data science/chemometrics or equal experience
- Good understanding of the Six Sigma processes and tools
- 10 years of experience in industrial development/R&D
- Strong leadership skills
- Structured and organised team player
- Creative and problem solver
- Strong communication skills
- Fluent in English, both verbally and in writing


DESIRED :
- Certified SixSigma Black Belt, or proven equivalent competence
- Expert knowledge of Multivariate data analysis (MVDA) and Design of experiments (DoE)
- Programming skills, e.g. LabView, MatLab, Python
- Experience in Machine learning or similar techniques
- Experience from development of separation products
- Fluent in Swedish, both verbally and in writing


Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.


For questions please contact hiring manager Ingrid Porrvik, [email protected] Please apply no later than June 7. We will interview continuously. Visa mindre

HR Reporting & Analytics Lead

Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing innov... Visa mer
Help us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.
We are looking for a HR Reporting & Analytics Lead to work with our expert HR team of 60+ employees across the world. Do you have a passion for analytics, reporting and projects? Then we would love to hear from you.
What you’ll do
• 'Go to' person for all reporting and analytics related matters, supporting reporting requirements needed by the HR organization.
• Understand employee life cycle transition processes and provide support to local team to ensure smooth transacting
• Develop expertise in the range of tools available to the wider HR team including team support on our HCM tool (Workday), in particular the reporting capability Manage complex data and information, providing analytics and reporting support
• Ability to support other operations related projects on HR tools, systems and processes
Who you are
• Strong analytical cability and comfortable working with HR data Experience with working with HCM / HR databases (Workday an advantage)
• Expert skills in Excel (can make data dance)
• Demonstrated ability in developing new proceses and improving current ones in an HR context
• Work on various projects to support the stand up of the Cytiva HR Operations and Total Rewards team
• Approachable and responsive
• Strong problem-solving skills; ability to make independent decisions, manage conflicting priorities in a fast paced environment
Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.
Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page!
Cytiva is a 3.5 billion USD global life sciences leader with over 7000 associates across 40 countries who are dedicated to our mission to help us improve access to life-changing therapies that transform human health. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients.
Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world.
Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here. Visa mindre

Site Communicator

Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing in... Visa mer
Help us improve access to life-changing therapies that can transform human health


We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.


Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.
We are looking for a communications professional to work with our expert team of 6700 employees across the world. Do you have a passion for scientific communication? Then we would love to hear from you.


What you’ll do
Deliver internal communications priorities across Cytiva Uppsala and Umeå site, often leading by example
Work closely with the regional leadership and other colleagues and across global communications, marketing and marketing communications to shape and deliver our message to stakeholders including partners, government bodies, and society.
Own particular communications projects and leadership of crisis and issues communication for Uppsala and Umeå
Leverage digital and social media channels to amplify storytelling and measure outcomes and effectiveness of targeting across internal audiences
Develop and implement meaningful and actionable metrics and considered evaluation of communications activities that consistently demonstrate the effectiveness of communications campaigns to the wider business



Who you are
Bachelor’s degree in Communications, Public Relations, English, Marketing, or a related field and five years communications experience
Excellent verbal and written communications skills, storytelling ability and presentations skills in both English and Swedish
Strong and proven communications leadership credentials in large multi-stakeholder organization
Dynamic, results focused and able to juggle priorities while building and maintaining trust and respect both within and outside the business; consistently delivering high quality results
Ability to offer communications counsel at leadership level
Able to clearly communicate complex information in an easy to understand manner
Clear interest and understanding of current affairs, politics and public opinion and the ability to gauge the effects of these on present and future business plans
Integrity: accepting and adhering to high ethical, moral, and personal values in decisions, communications, actions, and when dealing with others



Last date to apply is June 14. The interview process can start before that date.


Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career. Visa mindre

IT Infrastructure Engineer Network

Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing in... Visa mer
Help us improve access to life-changing therapies that can transform human health


We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.


Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.
We are looking for a Senior IT Infrastructure Engineer to work with our experts in IT team of 200+ employees across the world. Do you have a passion for IT Infrastructure ? Then we would love to hear from you.


What you’ll do
•Build and manage IT network Infrastrucure (WAN/LAN)
•Manage strategic and tactical IT planning for defined process area
•Understand business needs and map them into right IT solutions
•Lead small project initiatives both on local level and global level within IT Infrastructure area
•Work closely with the teams for delivery and operation to support quality in delivery of solutions and continuous excellence of support of solutions


If you have question related to this role, please contact hiring manager Björn Olsson ([email protected]).


Who you are
•Minimum of 8 years of experience
•Expertise in network topology (Cisco) and concepts with different devices such as network switches, router, fiber channeland Firewall (Palo Alto and CheckPoint)
•CCNA and/or CCNP certified
•Expertise in WiFi Infrastructure
•Strong collaboration and communication skills
•Expertise in ITIL Foundation
•Proficient at operating within a globally distributed team
•Fluency in English, good command of Swedish


Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career. Visa mindre

Supply Chain Finance Manager

Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing in... Visa mer
Help us improve access to life-changing therapies that can transform human health


We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.


Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.


What You'll Do
The Supply Chain Finance Manager is responsible for providing strategic P&L or operations finance leadership, for the manufacturing unit in Uppsala. The manufacturing unit is a chemical production facility which manufacture chromatography resins used in the purification processes of over 90% of all licensed biopharmaceuticals. The manufacturing unit has ~460 employees and produces >270 intermediates and >1700 end-products. The Supply Chain Finance Manager serves as a business partner to the manufacturing operating teams to drive manufacturing related initiatives, plant strategy, and profitability.


In this role you will
Partner with manufacturing leadership team and staff to drive operating performance & act as finance champion for strategic initiatives within the manufacturing organization
Own the processes for developing manufacturing estimates, operating plans/forecasts/reviews,
Drive profitable growth by providing quality financial analysis of results and reporting key metrics while advising the leadership team on risks and opportunities, as well as recommending actions
Actively participate with the manufacturing management to improve productivity and inventory management.
Provide Finance leadership for strategic investments impacting the manufacturing unit, for ex. large Investment projects, insourcing opportunities, new products.
Develop and improve financial processes: Finance reporting tools, Management reporting tools, budgeting and estimating processes, standard Production Cost set ups and analyses.
Effectively manage/lead/coordinate/develop a team of two financial analysts.



Who you are
We are seeking an experienced finance manager with a bachelor’s degree in Accounting, Finance, or Business Administration and minimum ten years work experience from developing forecasts & operating plans and leading business / finance reviews in industrial companies. You have minimum of five years’ experience from manufacturing finance and understand concepts such as product costing, productivity etc.
You are fluent in English as well as Swedish and have strong excel skills and experience with financial systems/applications (i.e.: Oracle, SAP, COGNOS, Business Objects, etc.)
As a leader you have experience from leading team members balancing execution through others with inclusiveness, leveraging expertise, clear thinking, imagination, and external focus.
As a person you have strong analytic skills and can clearly link financial results to operational performance drivers, generate alternatives and drive positive change. You also have strong influencing skills across business functions and excellent communication skills with ability to clearly communicate complex financial information in an easy to understand manner. You are a clear thinker and problem-solver and keep an open mind to change. Important is also that you have a high integrity, i.e. accepting and adhering to high moral, ethical, and personal values in decisions, communications, actions, and when dealing with others.


Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.


For questions please contact hiring manager Ann-Christine Löfgren, [email protected] +46 (0) 70 612 10 68 Visa mindre

Systemingenjör

Vill du vara med och ta det digitala språnget i vår världsledande produktionsanläggning i Uppsala? Nu utökar vi vårt professionella supportteam! Cytiva – tidigare GE Healthcare Life Sciences - söker nya medarbetare som är med och tar vår världsledande produktion in i nästa era. Vi inom System Support & Development tar ansvar för drift, support och utveckling av det digitala landskapet inom den kemiska produktionen i Uppsala. Just nu befinner vi oss i en sp... Visa mer
Vill du vara med och ta det digitala språnget i vår världsledande produktionsanläggning i Uppsala? Nu utökar vi vårt professionella supportteam!
Cytiva – tidigare GE Healthcare Life Sciences - söker nya medarbetare som är med och tar vår världsledande produktion in i nästa era. Vi inom System Support & Development tar ansvar för drift, support och utveckling av det digitala landskapet inom den kemiska produktionen i Uppsala. Just nu befinner vi oss i en spännande utrullning 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 vårat team med nya engagerade specialister.
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 systemingnejör är du en viktig del i teamet för att säkra driften och utvecklingen av våra produktionssystem.
Vi är mitt i en spännande resa som tar oss in i en digital produktion i världsklass. Vi söker nu dig som systemingenjör att vara en i teamet på denna resa.
Arbetsuppgifterna består bland annat av:
Supportera verksamheten och utföra avhjälpande åtgärder
Systemunderhåll och uppgraderingar
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 metodisk arbetssätt och har lätt för att se samband hur olika operationer hänger samman.
Din bakgrund
Examen från högskola eller universitet med relevant inriktning, eller erfarenhet från arbete i liknande roll, eller mångårig erfarenhet som sytemingenjör med ansvar för produktionskritiska system.
Ett brinnande intresse för digitalisering
Sytembakgrund från något av områdena automation, analytics eller information management. Andra systemerfarenheter är också intressanta.
Livscykelaktiviteter kopplade till system
Det är naturligt för dig att kommunicera på Svenska och Engelska.

Meriterande erfarenheter
Kunskap om systemintegration
Erfarenhet av supportverksamhet och aktiv systemförvaltning
Erfarenhet från produktions IT som nätverk, server och AD
Kunskap om validering av IT system

Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here.
Apply Now Save Visa mindre

Validation Engineer

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. Som tidigare del av GE Healthcare har vi ett rikt arv av värdefull erfarenhet och en nystart sedan 2020. Våra kunder bedriver livsavgörande forskning och produktion, alltifrån biologisk forskning till utveckling av nya vacc... 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. Som tidigare del av GE Healthcare har vi ett rikt arv av värdefull erfarenhet och en nystart sedan 2020.


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.


Dina arbetsuppgifter
Valideringsgruppen inom Chemical Production Uppsala (CPU) söker en engagerad och driven valideringsingenjör, gärna med erfarenhet från bioteknik, läkemedels- eller processindustri.
Avdlningen Process & Digital Support, där bl a valideringsgruppen ingår, är en supportorganisation till produktionen.


Gruppen består idag av nio valideringsingenjörer (den tjänst vi söker är en ersättning). Produktionen i Uppsala expanderar och installationsprojekt pågår vilket gör att det finns möjligheter till medverkan i större projekt och stora möjligheter till att utvecklas inom valideringsområdet.
Dina huvudsakliga arbetsuppgifter som valideringsingenjör är att:


planera, utforma och genomföra valideringar både i linjen och i större projekt.
delta i och driva utveckling och förbättring av instruktioner/arbetssätt inom ansvarsområdet.
bedöma valideringskrav för nya produkter och utrustningar samt vid förändringar.
presentera valideringsdokumentation vid audit.



Vem är du
Teknisk/Naturvetenskaplig universitetsexamen gärna civilingenjör eller motsvarande.
Erfarenhet från bioteknik, läkemedels- eller processindustri.
Goda kunskaper om valideringsprinciper, gärna erfarenhet av validering av datoriserade/automationssystem inom produktion, vattenvalidering, steriliseringsvalidering, rengöringsvalidering, processvalidering samt installations- och funktionskvalificering.
Mycket goda kunskaper i svenska och engelska, såväl muntligt som skriftligt.



Vi söker dig som är drivande och ansvarstagande. 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 noggrann och strukturerad med en naturlig förmåga att beskriva valideringars syfte och resultat på ett tydligt och överskådligt sätt.


Vilka är vi?
Oavsett din roll, ger vi dig ett syfte och en utmaning varje arbetsdag. Om du drivs av att göra världen till en bättre plats genom vetenskap och medicin, kommer du att känna dig hemma här. Är du flexibel, nyfiken och envis är du rätt person. Trivs du dessutom i en global kultur, kan detta vara platsen för din fortsatta karriär.


För frågor rörande tjänsten kontakta. Sofia Strömberg, [email protected], 070-3725764. Sista ansökningsdag är 14 juni. Visa mindre

Automationsingenjör

Vill du vara med och ta det digitala språnget i vår världsledande produktionsanläggning i Uppsala? Nu utökar vi vårt professionella supportteam! Cytiva – tidigare GE Healthcare Life Sciences - söker nya medarbetare som är med och tar vår världsledande produktion in i nästa era. Vi inom System Support & Development tar ansvar för drift, support och utveckling av det digitala landskapet inom den kemiska produktionen i Uppsala. Just nu befinner vi oss i en sp... Visa mer
Vill du vara med och ta det digitala språnget i vår världsledande produktionsanläggning i Uppsala? Nu utökar vi vårt professionella supportteam!
Cytiva – tidigare GE Healthcare Life Sciences - söker nya medarbetare som är med och tar vår världsledande produktion in i nästa era. Vi inom System Support & Development tar ansvar för drift, support och utveckling av det digitala landskapet inom den kemiska produktionen i Uppsala. Just nu befinner vi oss i en spännande utrullning 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 vårat team med nya engagerade specialister.
Automationsingenjör
För att supportera och säkerställa driften inom vår storskaliga proteinproduktion söker vi en automationsingenjör. Som automationsingenjör ansvarar du för support och förvaltning av installationen. Likaså är du en viktig kugge i vårat team och delaktig i arbetet med att supportera, utveckla och implementera sitens automationsstrategi.
Arbetsuppgifterna består bland annat av:
Supportera verksamheten och utföra avhjälpande åtgärder.
Nyckelroll i projekt för att säkra sitens automationsstandard när verksamheten växer.
Leda och operativt utföra aktiviteter kopplade till vår automationsstrategi.
Utveckla automationsområdet för bättre funktionalitet, operatörsupplevelse och output.
Tillsammans med systemleverantörer säkerställa rutiner, dokumentation och support

Rollen erbjuder stora möjligheter att vara del av den digitala utvecklingen av produktionen. Du kommer både att leda aktiviteter men också vara specialisten som säkerställer automationsfunktionalitet i anläggningarna och i projekt.
Inom avsnittet storskalig proteinproduktion är det flera styrsystem som samverkar varför erfarenhet av systemintegration är meriterande.
Du är självklart lösningsorienterad, serviceminded och ser vikten av att arbeta förebyggande för att skapa en driftsäker anläggning.
Din bakgrund
Examen från högskola eller universitet med relevant inriktning, eller erfarenhet från arbete i liknande roll, eller mångårig erfarenhet från produktion där automationssystem är ett dagligt verktyg
Kunskaper om Scada och DCS, med fördel Siemens S7 och ABB 800xA
Kunskap om systemintegration
Ett brinnande intresse för digitalisering
Det är naturligt för dig att kommunicera på Svenska och Engelska.
Goda kunskaper i planering och genomförande

Meriterande erfarenheter
Erfarenhet från processindustri
Erfarenhet av supportverksamhet och aktiv systemförvaltning
Brett kontaktnät i branchen
Kunskap om BioSCADA och/eller Unicorn

Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here. Visa mindre

Process Engineer

Vi söker nu en Processingenjör till vår storskaliga kemiska produktion i Uppsala. Detta är ett vikariat på 6 månader. Arbetsuppgifter Supporta i implementeringen av ny teknologi processansvarig för förbättringsarbete Utreda ärenden inom kvalitét Öka produktiviteten genom att skala upp processer, materialbesparingar, korta ner ledtider etc. Vem är du? • Du har en universitetsexamen inom kemi eller liknande område. • God kommunikationsförmåga i bå... Visa mer
Vi söker nu en Processingenjör till vår storskaliga kemiska produktion i Uppsala. Detta är ett vikariat på 6 månader.


Arbetsuppgifter
Supporta i implementeringen av ny teknologi
processansvarig för förbättringsarbete
Utreda ärenden inom kvalitét
Öka produktiviteten genom att skala upp processer, materialbesparingar, korta ner ledtider etc.


Vem är du?
• Du har en universitetsexamen inom kemi eller liknande område.
• God kommunikationsförmåga i både tal och skrift
• Intresserad av storskalig produktion
• En sann lagspelare
• Bra på att ta egna initiativ
• Bra på att arbeta med flera projekt samtidigt

Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.

Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page!

Cytiva is a 3.5 billion USD global life sciences leader with over 7000 associates across 40 countries who are dedicated to our mission to help us improve access to life-changing therapies that transform human health. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients. Visa mindre

Mechanical Engineer

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. Som tidigare del av GE Healthcare har vi ett rikt arv av värdefull erfarenhet och en nystart sedan 2020. Våra kunder bedriver livsavgörande forskning och produktion, alltifrån biologisk forskning till utveckling av nya vaccin... 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. Som tidigare del av GE Healthcare har vi ett rikt arv av värdefull erfarenhet och en nystart sedan 2020.
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.
Dina arbetsuppgifter
QCs huvudsakliga syfte är att kvalitetskontrollera tillverkade intermediat och slutprodukter, vilket innefattar att registrera och förbereda prover, utföra analyser, bedöma och värdera resultat samt besluta om och rapportera produkternas analysresultat.
Dina huvudsakliga arbetsuppgifter innebär att:
Kvalitetskontrollera produkter, vilket innefattar att enligt fastställda metoder
Registrera analys- och referensprover
Utföra analyser
Sammanställa, kontrollgranska, utvärdera, godkänna, avrapportera, acceptera ut och arkivera resutat
Kalibrera, kontrollera och underhålla instrument
Utreda och rapportera avvikelser
Allmän service, såsom att beställa och mottaga kemikalier, hantera avfall mm
Förbättra processer och rutiner i alla steg inom verksamhetsområdet
Uppdragsanalysera och avrapportera
Lära upp personal på analyser där den egna kompetensen är god
Rapportera avvikelser i Trackwise och utföra labutredningar
Representera sektionen inom företaget samt gentemot externa kunder och leverantörer

Vem är du
Du har en högskoleexamen inom relevant teknikområde (kemi/bioteknik/biologi) eller annan lämplig utbildning kombinerad med erfarenhet från bioteknisk eller läkemedelsindustri.
God samarbetsförmåga
Resultat- och målinriktad
Förändringsbenägen
God förmåga att uttrycka sig i tal och skrift på svenska och engelska
Ansvarstagande
Noggrann

För frågor rörande tjänsten, kontakta rekryterande chef Thomas Ekström på [email protected]
Vilka är vi?
Oavsett din roll, ger vi dig ett syfte och en utmaning varje arbetsdag. Om du drivs av att göra världen till en bättre plats genom vetenskap och medicin, kommer du att känna dig hemma här. Är du flexibel, nyfiken och envis är du rätt person. Trivs du dessutom i en global kultur, kan detta vara platsen för din fortsatta karriär.
Vill du veta mer? Spana in vår Careers webbsida, Instagram-kanal och LinkedIn-sida! Visa mindre

Drifttekniker Reningsverk och Miljö

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. Som tidigare del av GE Healthcare har vi ett rikt arv av värdefull erfarenhet och en nystart sedan 2020. Våra kunder bedriver livsavgörande forskning och produktion, alltifrån biologisk forskning till utveckling av nya vaccin... 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. Som tidigare del av GE Healthcare har vi ett rikt arv av värdefull erfarenhet och en nystart sedan 2020.
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.
Dina arbetsuppgifter
Vi söker en Drifttekniker till Reningsverk & Miljö sektionen inom Kemisk Produktion Uppsala.
Sektionen Reningsverk & Miljö ansvarar för:
sitens luftemissioner
sitens processavloppsvatten
renvattenfrågor för produktion

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.
Processavloppsvattnet renas med tre olika förbehandlingar och en biologisk rening.
Luftemmssioner renas med ett kolfilter och kondensorer, och sitens utsläpp mäts kontinuerligt.
Som Drifttekniker arbetar du med:
Provtagning, provhantering och driftsuppföljning av både luft- och vattenemissioner.
Drift och underhåll av reningsanläggningar, pumpstationer och rörsystem.
Övervakar anläggningarna, köra processer och säkerställer driften.
Utför regelbunden rondering och underhållsarbeten.
Utför kalibreringar av olika instrument.
Deltar i projekt som berör sektionen.
Jobbar med ständiga förbättringar.
Deltar i EHS-relaterade ärenden.
Vidtar åtgärder för att förhindra oförutsedda utsläpp till omgivningmiljön.

Vem är du
Erfarenhet från Reningsverk alt mot processindustrin
Erfarenhet från kemikaliehantering och Ex-miljö
Erfarenhet från styrsystem eller övervakning av processer
Kunna arbeta både självständigt och i grupp
Kunna ta egna initiativ och fatta beslut.
God problemlösningsförmåga.
Goda kunskaper i engelska och svenska.
Vilka är vi?
Oavsett din roll, ger vi dig ett syfte och en utmaning varje arbetsdag. Om du drivs av att göra världen till en bättre plats genom vetenskap och medicin, kommer du att känna dig hemma här. Är du flexibel, nyfiken och envis är du rätt person. Trivs du dessutom i en global kultur, kan detta vara platsen för din fortsatta karriär.
För frågor rörande tjänsten kontakta. Sara Wibäck, [email protected], 0706721516
Vill du veta mer? Spana in vår Careers webbsida, Instagram-kanal och LinkedIn-sida! Visa mindre

Data Scientist / Lead Black Belt

Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing in... Visa mer
Help us improve access to life-changing therapies that can transform human health


We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.


Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.


What You'll Do
You will, as part of R&D, contribute to the development of new products which are used in the manufacturing of leading biological drugs. Your tasks will include work all the way from idea generation, research and development work and finally transfer to production scale. You will also take active part in trouble shooting of existing Cytiva and customer processes. The Uppsala Cytiva site is a workplace for more than 1200 persons 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.
More specifically will your tasks include:
- Drive and foster a data driven culture including Six Sigma processes and tools within RnD
- Leadership in value-creation from smart data management
- Perform data analysis in development project and trouble-shooting activities
- Setting up structured experimental plans
- Identify, implement new techniques and follow the technical development in the field
- Independently plan and accomplish given tasks, to reach given project objectives
- Independently solve problems of “trouble shooting character” in project work
- Document and report results both orally and written


Who you are
- Master degree in engineering or technical discipline with expert competency in data science/chemometrics or equal experience
- Good understanding of the Six Sigma processes and tools
- 10 years of experience in industrial development/R&D
- Strong leadership skills
- Structured and organised team player
- Creative and problem solver
- Strong communication skills
- Fluent in English, both verbally and in writing


DESIRED :
- Certified SixSigma Black Belt, or proven equivalent competence
- Expert knowledge of Multivariate data analysis (MVDA) and Design of experiments (DoE)
- Programming skills, e.g. LabView, MatLab, Python
- Experience in Machine learning or similar techniques
- Experience from development of separation products
- Fluent in Swedish, both verbally and in writing


Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.


For questions please contact hiring manager Ingrid Porrvik, [email protected] Please apply no later than June 7. We will interview continuously. Visa mindre

Cell Culture Field Application Specialist

Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing inno... Visa mer
Help us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.


Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.
We are looking for a Cell Culture Field Application Specialist to work with our sales and technical experts in the Cell Culture Commercial Modality team of 20 field base employees spread across EMEA. Do you have a passion for the Biopharmaceutical Industry? Then we would love to hear from you.


What you’ll do
Primary responsibility is to provide troubleshooting and application support on issues that arise related to end-user’s technical skills, feeding strategies, experiment of design and explaining technical results from optimization/support services.
Provide technical support during sales process by demonstrating full range of product features including potential uses, product capabilities and benefits to customers as needed
Work closely with our Process Science Leaders to identify custom media development projects and provide technical support relating to media optimization and formulation modifications for our customers.
Support trade shows and professional conferences by performing product demonstration and seminars
Use market and product knowledge to assist sales teams in developing sales, marketing and account sales strategies
Provide competitive product insight and provide regular feedback on customer satisfaction and needs to internal stakeholders.
Support Account Managers and Sales Specialists across all BioPharma functions to develop and finalize bids/quotes and custom services to meet customer requirements.



Who you are
A Masters or PhD degree in Life Sciences or Biomedical Engineering or related discipline. However, would consider graduate level if experienced in Bioprocess.
Must have 5+ years of industry experience in cell culture process development and/or manufacturing within a pharmaceutical/biotechnology company
Demonstrated interpersonal & communication skills (ability to effectively communicate, verbally and in writing, to external customers, global counterparts and to team members in other functional organizations)
Solid problem-solving skills (ability to manage and resolve conflict, communicate issues and propose solutions to both internal team members and external customers)
Willingness to travel within your specified geographic region and globally to participate in trainings, meetings and key projects.
Proven professional business acumen (experience interfacing with both internal team members and external customers as a part of a solution-based sales process)
Good communication, interpersonal and negotiating skills and high ability to work in a team.
Self-motivated, willingness to take the initiative to identify opportunities for improvement and take actions to improve.
Proficiency in computer skills in Microsoft Office Suite products.
Fluency in English (written and spoken). Additional language skill would be beneficial.
To the extent you are applying for a position that requires you to operate a Cytiva owned/leased, privately owned/leased or rental vehicle for company business, you must be willing to submit to a check of your driving record.
Must be willing to travel (~20 - 60%)

For questions in regards to this opening, please contact hiring manager Vicky Thomson ([email protected]). Last day to apply is June 7.


Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career. Visa mindre

Regulatory Support Manager

Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing inn... Visa mer
Help us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.

Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.

We are looking for a Regulatory Support Manager to work with our expert Customer Regulatory Support team of 15 employees across the world. Do you have a passion for understanding customer situations and needs, and supporting customers? Then we would love to hear from you.

What you’ll do
• Participate in projects to develop regulatory support documentation for products in customers regulated environments, and update after launch
• Perform necessary investigations, and prepare and deliver statements and certificates
• Respond efficiently and promptly to customers regulatory/quality based issues
• Participate in change control cases, be the customer advocate, prepare and publish the change notification letter or package
• Participate in creating and updating processes, guidelines and steering documents

Who you are
• Bachelor of Science degree in Chemistry, Pharmacy or other related field
• Five or more years of experience in quality, product management or other related field for understanding of GMP and regulatory requirements in the bioprocess industry
• Excellent English and Swedish level
• Organized, accurate, target oriented, quality minded and customer oriented
• Strong written and verbal communication skills
• Flexible and service minded with the ability to collaborate
• Strong ability to work independently, drive

For questions related to this opening, please contact hiring manager Ondina Åsberg ([email protected]). Please apply no later than June 14. Interviews will happen continuously.


Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career. Visa mindre

Global Product Manager UNICORN

Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing inn... Visa mer
Help us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.

Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.

We are looking for a Product Manager for UNICORN to work with our expert UNICORN Product Management team of 3 employees across the world. Do you have a passion for Software Product Management? Then we would love to hear from you.

What you’ll do
• Driving the product portfolio to meet the needs of the market
• Responsible for strategy and execution of the product roadmaps and new product introductions
• Work closely with engineering to ensure that at each step of development that requirements are met
• Conduct product research to understand the marketplace and opportunities for growth
• Coordinate product requirements across a multi-functional organization, including marketing, sales, operations, engineering, and services teams, while ensuring compliance with quality systems and regulatory requirements

Who you are
• 15+ years' experience in the software industry, product development or related field.
• Deep Product Management/Marketing expertise, including: market trends/analysis, NPI process, product roadmap development, requirements, product life-cycle management,
• Software product/industry/technical acumen
• Leadership skills to lead teams and shape/lead growth vision and marketing strategy
• Innovation – develop new ideas through collaboration and execute on creative ideas
• Team oriented – ability to motivate and work well with diverse, cross-functional teams
• Proven ability to influence and negotiate internally and with customers

Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.


For job related questions, please contact hiring manager Chris Sandusky ([email protected]). Please submit your application no later than June 7. Interviews are happening continuously. Visa mindre

Senior Process- & Systems Leader PLM

Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing in... Visa mer
Help us improve access to life-changing therapies that can transform human health


We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.


Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.


What you'll do


The PLM function within Cytiva consists out of 15 employees who work globally with systems such as MAGIC (Enovia PLM), xCAD and Configurator. As a Senior Process & System Leader you will work with the business and IT to ensure strategic, tactical and operational alignment in order to standardize process and drive product modularization.
Additional responsibilities are:


Develop processes (mainly design related) and associated system capabilities (mainly MAGIC) to maximize productivity, whilst ensuring compliance, scalability/growth and alignment with overall Cytiva priorities
Support relevant businesses and functions with translation of their needs and requirements into program- and jobjar requests to be delivered by IT
Drive/enforce process standardization and product modularization to enable growth and ultimately improve outcome for our customers and the business
Translate business needs and functional requirements into enhancement requests to be delivered by IT (or Cloud/SaaS vendors).
Global User Council Chairman for Engineering- & Variant Management and be active in the global Governance Board (MAGIC platform)



Who you are
University degree in Engineering/Technology or related field / or equivalent knowledge or experience
Experience in product development as well as solid knowledge of Product Modularization concepts is considered as an advantage
Proven ability to work with cross-functional, multi-cultural teams and deliver results in an ambiguous-, dynamic- and multi-stakeholder environment. Skilled Coach, Influencer and Change Agent
Excellent written and verbal communication skills; fluent in English (oral and written)



Desired Characteristics
Major experience from standardization, process- and systems improvements
Skilled Lean Leader/Facilitator
Strong communication, interpersonal, analytical and problem-solving skills
Willing to travel domestically and internationally when required



Who we are


Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career. Visa mindre

Senior Research Engineer

Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing in... Visa mer
Help us improve access to life-changing therapies that can transform human health


We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.


Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.
We are looking for a Research Engineer / Senior Research Engineer to work with our expert Sensor Technologies Team in Bioprocessing R&D, Uppsala, Sweden. The primary focus of this position is to plan and perform engineering activities in the fermentation area from lab scale to bioreactors in large scale.
This position also requires root cause analysis investigation, data analysis and report writing to resolve and improve product design, process and quality issues all while working in a cross-functional team environment in close collaboration with Manufacturing and Quality departments.
Do you have a passion for bioreactor cultivation and process development? Then we would love to hear from you.
The selection process will be ongoing during the application period. Last application day 21 june 2020.
What You'll Do
Design, perform, analyze, document and present fermentation of recombinant proteins in different formats, from lab scale to bioreactors in large scale.
Develop, invent and improve new products and processes for the bioprocess industry, specifically within the fields of affinity ligands. To independently or in a team plan accomplish given tasks from Project Manager or Section Manager, to reach given project objectives. Report accomplished tasks in writing (e.g. Technical Report) or orally.
Provide technical expertise within the areas of bacterial fermentation and process development of recombinant proteins and solve technical problems, supporting both internal production and customers
Act as team member or Design responsible in NPI and Market Support projects
Present scientific and technical results internally, both in oral and written communication in Swedish and English

Who you are
In order to succeed in this position, you need to be 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, plan, perform, analyze, document and present results to progress our projects forward.
Bachelor or Master’s degree in biology, medicine, engineering or related Life Science field or equal experience in related fields or equivalent knowledge or experience.
Experience in bacterial cell culturing in different formats, including bioreactor cultivation.
Experience in culture and process development for production of recombinant proteins.
Experience in industrial scale microbial cultivation is a plus
Experience from industrial development/ R&D within medicine, biotechnology or bioprocess is a plus
Experience in different analytical techniques is a plus
Experience in cultivation of mammalian cells is a plus
Occasional work on weekends may occur

Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.

For questions please contact hiring manager Yvette Klingberg, [email protected]
Want to know more? Take a look at our Careers website, Instagram and LinkedIn page! Visa mindre

Laboratory Specialist

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. Som tidigare del av GE Healthcare har vi ett rikt arv av värdefull erfarenhet och en nystart sedan 2020. Våra kunder bedriver livsavgörande forskning och produktion, alltifrån biologisk forskning till utveckling av nya vacc... 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. Som tidigare del av GE Healthcare har vi ett rikt arv av värdefull erfarenhet och en nystart sedan 2020.


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.


Dina arbetsuppgifter
Vi söker laboratorieingenjör (Laboratory Specialist) som ska kvalitetskontrollera produkter från vår produktion av kromatografimedia inom Chemical Production Uppsala (CPU).
I rollen som laboratorieingenjör arbetar du främst med att kvalitetskontrollera produkter enligt gällande instruktioner och rutiner samt bedöma om analysstatus. De analystekniker som används mest är titrering och kromatografi. Andra arbetsuppgifter är;
- Starta och driva undersökningar vid avvikande analysresultat och andra avvikelser.
- Utföra kontroller, kalibreringar och underhåll av analysinstrument.
- Uppdatera och godkänna arbetsinstruktioner.


Vem är du
Lämplig bakgrund är högskoleingenjör/ gymnasieingenjör inom Kemi/Analytisk Kemi/ Biokemi eller liknande. Tidigare erfarenhet från arbete på kvalitetslaboratorie är ett plus.

Vi söker någon som är:
• noggrann och strukturerad
• flexibel
• bra på att samarbeta
• positiv, uppmuntrar och inspirerar andra
• stresstålig och kan utföra flera olika arbetsuppgifter parallellt
• gillar att arbeta i förändring och driva förändringsarbete


Vilka är vi?
Oavsett din roll, ger vi dig ett syfte och en utmaning varje arbetsdag. Om du drivs av att göra världen till en bättre plats genom vetenskap och medicin, kommer du att känna dig hemma här. Är du flexibel, nyfiken och envis är du rätt person. Trivs du dessutom i en global kultur, kan detta vara platsen för din fortsatta karriär.


För frågor rörande tjänsten kontakta. Sten Ivarsson [email protected]/+46706120973
Sista ansökningsdag är den 31 maj. Visa mindre

Project Manager

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. Som tidigare del av GE Healthcare har vi ett rikt arv av värdefull erfarenhet och en nystart sedan 2020. Våra kunder bedriver livsavgörande forskning och produktion, alltifrån biologisk forskning till utveckling av nya va... 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. Som tidigare del av GE Healthcare har vi ett rikt arv av värdefull erfarenhet och en nystart sedan 2020.


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 nu en Project Manager till avdelningen Projects. Avdelningen ansvarar för tekniska anläggnings/investeringsprojekt inom Site Uppsala. Befattningen omfattar att driva investeringsprojekt operativt och affärsmässigt mot överenskomna mål.


Dina arbetsuppgifter


Ansvara för att erfoderliga mål definieras och erfoderliga planer upprättas,
Leda det dagliga arbetet i investeringsprojekt och att projektarbetet följs upp och styrs kontinuerligt.
Svara inför beställaren för att de uppställda målen i projektet blir uppfyllda.
Att tillsammans med verksamheten välja teknisk lösning för projektet.
Ansvara för att projektintressenter får erfoderlig information.
Bidra aktivt till utvecklingen inom Projects.



Som Project manager ansvarar du för


att en projektplan utarbetas och följs upp.
att uppdraget genomförs enligt beställarens funktionskrav och specifikationer och tillämpliga direktiv och policys.
att projekten ges en tekniskt, tidsmässigt - ekonomiskt optimal totalutformning.
att ansvara för avtal och avtalsändringar med konsulter, entreprenörer och leverantörer.
att projektarbetet drivs rationellt med rätt avvägda resursinsatser.
att lagar, bestämmelser och myndigheters krav på projektarbetet och den färdiga anläggningen tillgodoses.
att via lägesrapporter hålla beställare (projektchef/styrgrupp) informerad om projektets utveckling.
att projektintressenter får erforderlig information.



Vem är du


Du har adekvat ingenjörsutbilning och goda kunskaper i engelska. Du kommer med erfarenhet från projektledning, processindustri och budget och ekonomisk uppföljning. Vi söker dig som är


Målinriktad, affärsmässig och beslutsam.
Självgående.
Strukturerad/analytisk.
Samarbetsförmåga
Goda kommunikationsegenskaper internt och externt.
Initiativrik i både ord och handling.



För mer information kontakta rekryterande chef Petra Olsson +46 738681650 eller [email protected] Välkommen med din ansökan senast den 31 maj.


Vilka är vi?


Oavsett din roll, ger vi dig ett syfte och en utmaning varje arbetsdag. Om du drivs av att göra världen till en bättre plats genom vetenskap och medicin, kommer du att känna dig hemma här. Är du flexibel, nyfiken och envis är du rätt person. Trivs du dessutom i en global kultur, kan detta vara platsen för din fortsatta karriär. Visa mindre

Processoperatör

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. Som tidigare del av GE Healthcare har vi ett rikt arv av värdefull erfarenhet och en nystart sedan 2020. Våra kunder bedriver livsavgörande forskning och produktion, alltifrån biologisk forskning till utveckling av nya vaccin... 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. Som tidigare del av GE Healthcare har vi ett rikt arv av värdefull erfarenhet och en nystart sedan 2020.
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 driven processoperatör till Affinitetssektionen inom Produktion Uppsala. Har du en passion för bioteknik? Då vill vi gärna höra ifrån dig.
Dina arbetsuppgifter
Storskalig kemiproduktion av kromatografiprodukter inom Affinitet-och HIC segmenten
Kalibrering av utrustning enligt metoder samt skötsel av utrustning och lokaler
Medverkande i förbättringsarbetet och problemlösningar rörande processer och utrustning

Vem är du
Vi söker dig som har gymnasieutbildning med inriktning mot kemi, processteknik eller liknande, eller motsvarande arbetslivserfarenhet
Erfarenhet av processindustri, gärna inom kemisk produktion och/eller läkemedelsproduktion med hög automationsgrad
Erfarenhet av arbete med automationssystem så som t ex receptbyggande är meriterande
Goda kunskaper i svenska och engelska
Du har ett gediget tekniskt intresse och drivas av att lära dig nya processer
Du är noggrann och har gott ordningssinne
Som person bör du vara driftig och initiativtagande med god kommunikations-och samarbetsförmåga
Du har god datorvana och gärna erfarenhet av outlook, word, excel och Oracle

Vilka är vi?
Oavsett din roll, ger vi dig ett syfte och en utmaning varje arbetsdag. Om du drivs av att göra världen till en bättre plats genom vetenskap och medicin, kommer du att känna dig hemma här. Är du flexibel, nyfiken och envis är du rätt person. Trivs du dessutom i en global kultur, kan detta vara platsen för din fortsatta karriär.
För frågor rörande tjänsten kontakta [email protected] Sista ansökningsdag är den 31 maj.
Vill du veta mer? Spana in vår Careers webbsida, Instagram-kanal och LinkedIn-sida!
Cytiva är en 3,3 miljarder USD global ledare inom biovetenskap med nästan 7 000 anställda i 40 länder som är hängivna vårt uppdrag att främja och påskynda behandlingar. Som en pålitlig partner till kunder världen över bidrar Cytiva till ett effektivt arbetsflöde till forskning och utveckling, säkerställer tillverkning och leverans av omvälvande mediciner till patienter.
Cytiva är en del av Danaher-familjen, en global nyskapare inom vetenskap och teknologi som är hängiven att hjälpa kunder att lösa komplexa utmaningar samt förbättra livskvaliteten välden över.
Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here. Visa mindre

Elektronikingenjör

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. Som tidigare del av GE Healthcare har vi ett rikt arv av värdefull erfarenhet och en nystart sedan 2020. Våra kunder bedriver livsavgörande forskning och produktion, alltifrån biologisk forskning till utveckling av nya vaccin... 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. Som tidigare del av GE Healthcare har vi ett rikt arv av värdefull erfarenhet och en nystart sedan 2020.
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.


Arbetsuppgifter
Vi söker en driven Elektronikingenjör till vår site i Uppsala. Du kommer att ingå i ett team med ingenjörer inom elektronik och mekanik som tillsammans utvecklar nästa generations system för läkemedlsframställning.
Du kommer att jobba med att utveckla elektronik för system som innehåller pumpar, sensorer, motorer, robotar. Arbetet innehåller hela kedjan från idé till färdig produkt. Kretskortsdesign (scheman och layout) är en viktig del i arbetet.


Vem söker vi?
Högskoleingenjör eller civilingenjör inom elektroteknik
Goda kunskaper i Svenska och Engelska är ett krav (tal och skrift)
Du är strukturerad, organiserad och en sann lagspelare med högt driv



Vilka är vi?
Oavsett din roll, ger vi dig ett syfte och en utmaning varje arbetsdag. Om du drivs av att göra världen till en bättre plats genom vetenskap och medicin, kommer du att känna dig hemma här. Är du flexibel, nyfiken och envis är du rätt person. Trivs du dessutom i en global kultur, kan detta vara platsen för din fortsatta karriär.
Vill du veta mer? Spana in vår Careers webbsida, Instagram-kanal och LinkedIn-sida!
Cytiva är en 3,3 miljarder USD global ledare inom biovetenskap med nästan 7 000 anställda i 40 länder som är hängivna vårt uppdrag att främja och påskynda behandlingar. Som en pålitlig partner till kunder världen över bidrar Cytiva till ett effektivt arbetsflöde till forskning och utveckling, säkerställer tillverkning och leverans av omvälvande mediciner till patienter. Visa mindre

Bioteknik ingenjör inom R&D

Vi söker en System Engineer till sektionen UX & System design, R&D i Uppsala. Som System Engineer får du möjlighet att arbeta med världsledande produkter inom Life Sciences, och att dagligen jobba tillsammans med fantastiskt duktiga och engagerade kollegor. Du kommer att vara involverad i produkternas hela livscykel från utveckling till underhåll och support. Sektionen ingår i avdelningen Downstream Systems som utvecklar instrument och mjukvara för vätskek... Visa mer
Vi söker en System Engineer till sektionen UX & System design, R&D i Uppsala.
Som System Engineer får du möjlighet att arbeta med världsledande produkter inom Life Sciences, och att dagligen jobba tillsammans med fantastiskt duktiga och engagerade kollegor. Du kommer att vara involverad i produkternas hela livscykel från utveckling till underhåll och support.
Sektionen ingår i avdelningen Downstream Systems som utvecklar instrument och mjukvara för vätskekromatografi (ÄKTA system och UNICORN software). Inom avdelningen har vi många olika kompetenser såsom mekanik, elektronik, system och applikation, och arbetar i nära samarbete med mjukvaruavdelningen Downstream Software. Utvecklingen bedrivs i ett agilt-ramverk med tvärfunktionella team där vi tar fram produkter för Life Sciences industrin och akademin.
Arbetsuppgifter
Du har stor förståelse för våra kunder och deras behov, och bidrar i alla faser av utvecklingen av våra produkter. Allt från att specificera användarens krav, ta fram test- och verifieringsplaner inklusive testprocedurer, till att utföra verifiering och validering av instrument och mjukvara, samt utveckla manualer och träningsmaterial.
Uppgifter inkluderar (men är inte begränsade till):
Som en del av ett team, planera och leverera teamets åtaganden
Skapa användar- och systemkrav för mjukvara samt procedurer för hur de ska verifieras
Planera, utföra och rapportera resultat från testning, verifiering och validering av system- eller subsystemkrav
I nära samarbete jobba med och stötta mjukvaruutvecklare i produktutvecklingen
Kontinuerligt förbättra våra arbetssätt



Ditt huvudfokus kommer att vara att aktivt bidra i leveransen av nya produkter till marknaden och våra kunder.
Kvalifikationer
MSc eller BSc inom bioteknik, kemiteknik eller liknande
Teoretisk kunskap och praktisk erfarenhet av proteinrening
Dokumenterad erfarenhet av att ha arbetat med produktutveckling
Strukturerad och organiserad lagspelare
Utmärkta kommunikations- och presentationskunskaper (både skriftliga och muntliga)
Svenska och engelska som arbetsspråk



Meriterande
För att vara en lämplig kandidat för jobbet är det även önskvärt att du är/har:
Förmågan att snabbt lära dig nya ämnesområden/verktyg/tekniker
Ett genuint intresse av mjukvaruutveckling från användarens perspektiv
Erfarenhet från arbete i en tvärvetenskaplig miljö
Resultatorienterad
Förmågan att arbeta självständigt och att driva arbetet framåt
Praktisk erfarenhet av ÄKTA plattformen och UNICORN

Arbetet bedrivs i nära samarbete med specialister från olika delar av R&D, såsom mekanik och elektronik, mjukvaruutvecklare och applikation varför det är önskvärt att sökande har intresse och insikt inom dessa områden. Visa mindre

Testledare / Software Test Engineer

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. Som tidigare del av GE Healthcare har vi ett rikt arv av värdefull erfarenhet och en nystart sedan 2020. Våra kunder bedriver livsavgörande forskning och produktion, alltifrån biologisk forskning till utveckling av nya vaccin... 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. Som tidigare del av GE Healthcare har vi ett rikt arv av värdefull erfarenhet och en nystart sedan 2020.
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 nu efter en Testledare/ Software Test Engineer som ska arbeta i våra team av utvecklare och testare av applikationsmjukvara för forskning och tillverkning av framtidens biologiska läkemedel. Vi är ungefär 80 utvecklare och testare världen runt. Har du en passion för mjukvarutestning och utveckling? Då vill vi gärna höra ifrån dig.
Dina arbetsuppgifter
Designa, genomföra och underhålla manuella och automatiserade testfall
Sätta uppoch underhålla testmiljöer och integrationer (system, operativsystem, webbläsaruppdateringar)
Bidra till testarkitektur och process, både manuell och automatiserad testning
Vara den ansvariga personen för alla testaktiviteter inom en releaseoch vägleda kollegor från andra kompetensområden.
Vara ansvarig för kvalitet, testanalys och testmetodik för programvaruprodukter

Vem är du
Du har minst en kandidatexamen inom mjukvaruutveckling eller jämförbar kompetensnivå.
Du har minst 2 års erfarenhet inom testningav mjukvara
Du har kunskap om testautomatiseringsverktyg som tex UFToch SpecFlowsamt testhanteringsverktyg ex. HP ALM
Du har flytande svenska och engelska (skriftligt och talat)
Du har förhoppningsvis erfarenhet av bra agil utveckling inklusive beteendedriven utveckling och testdriven utveckling, BDD och TDD
Gärna ett intresse för både mjuk-och hårdvaruapplikationer, med erfarenhet från kontrollmjukvarutestning, från enhet upp till systemtest.
Du gillar avancerade testfall och bidra till lösningen av buggar som hittats.

Vilka är vi?
Oavsett din roll, ger vi dig ett syfte och en utmaning varje arbetsdag. Om du drivs av att göra världen till en bättre plats genom vetenskap och medicin, kommer du att känna dig hemma här. Är du flexibel, nyfiken och envis är du rätt person. Trivs du dessutom i en global kultur, kan detta vara platsen för din fortsatta karriär.
För frågor rörande tjänsten kontakta rekryterande chef Åsa Nordstedt på: [email protected]
Vill du veta mer? Spana in vår Careers webbsida, Instagram-kanal och LinkedIn-sida!
Cytiva är en 3,3 miljarder USD global ledare inom biovetenskap med nästan 7 000 anställda i 40 länder som är hängivna vårt uppdrag att främja och påskynda behandlingar. Som en pålitlig partner till kunder världen över bidrar Cytiva till ett effektivt arbetsflöde till forskning och utveckling, säkerställer tillverkning och leverans av omvälvande mediciner till patienter.
Cytiva är en del av Danaher-familjen, en global nyskapare inom vetenskap och teknologi som är hängiven att hjälpa kunder att lösa komplexa utmaningar samt förbättra livskvaliteten välden över.
Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here.
Apply Now Visa mindre

System Engineer

Vi söker en System Engineer till sektionen UX & System design, R&D i Uppsala. Som System Engineer får du möjlighet att arbeta med världsledande produkter inom Life Sciences, och att dagligen jobba tillsammans med fantastiskt duktiga och engagerade kollegor. Du kommer att vara involverad i produkternas hela livscykel från utveckling till underhåll och support. Sektionen ingår i avdelningen Downstream Systems som utvecklar instrument och mjukvara för vätskek... Visa mer
Vi söker en System Engineer till sektionen UX & System design, R&D i Uppsala.
Som System Engineer får du möjlighet att arbeta med världsledande produkter inom Life Sciences, och att dagligen jobba tillsammans med fantastiskt duktiga och engagerade kollegor. Du kommer att vara involverad i produkternas hela livscykel från utveckling till underhåll och support.
Sektionen ingår i avdelningen Downstream Systems som utvecklar instrument och mjukvara för vätskekromatografi (ÄKTA system och UNICORN software). Inom avdelningen har vi många olika kompetenser såsom mekanik, elektronik, system och applikation, och arbetar i nära samarbete med mjukvaruavdelningen Downstream Software. Utvecklingen bedrivs i ett agilt-ramverk med tvärfunktionella team där vi tar fram produkter för Life Sciences industrin och akademin.
Arbetsuppgifter
Du har stor förståelse för våra kunder och deras behov, och bidrar i alla faser av utvecklingen av våra produkter. Allt från att specificera användarens krav, ta fram test- och verifieringsplaner inklusive testprocedurer, till att utföra verifiering och validering av instrument och mjukvara, samt utveckla manualer och träningsmaterial.
Uppgifter inkluderar (men är inte begränsade till):
Som en del av ett team, planera och leverera teamets åtaganden
Skapa användar- och systemkrav för mjukvara samt procedurer för hur de ska verifieras
Planera, utföra och rapportera resultat från testning, verifiering och validering av system- eller subsystemkrav
I nära samarbete jobba med och stötta mjukvaruutvecklare i produktutvecklingen
Kontinuerligt förbättra våra arbetssätt



Ditt huvudfokus kommer att vara att aktivt bidra i leveransen av nya produkter till marknaden och våra kunder.
Kvalifikationer
MSc eller BSc inom bioteknik, kemiteknik eller liknande
Teoretisk kunskap och praktisk erfarenhet av proteinrening
Dokumenterad erfarenhet av att ha arbetat med produktutveckling
Strukturerad och organiserad lagspelare
Utmärkta kommunikations- och presentationskunskaper (både skriftliga och muntliga)
Svenska och engelska som arbetsspråk



Meriterande
För att vara en lämplig kandidat för jobbet är det även önskvärt att du är/har:
Förmågan att snabbt lära dig nya ämnesområden/verktyg/tekniker
Ett genuint intresse av mjukvaruutveckling från användarens perspektiv
Erfarenhet från arbete i en tvärvetenskaplig miljö
Resultatorienterad
Förmågan att arbeta självständigt och att driva arbetet framåt
Praktisk erfarenhet av ÄKTA plattformen och UNICORN

Arbetet bedrivs i nära samarbete med specialister från olika delar av R&D, såsom mekanik och elektronik, mjukvaruutvecklare och applikation varför det är önskvärt att sökande har intresse och insikt inom dessa områden. Visa mindre

Processingenjör

Vi söker en processingenjör till sektionen Chip & IFC, inom Biacore consumables produktionen i Uppsala. Sektionen består av 1 chef, 2 ingenjörer och 14 operatörer. Tillverkningen består av Sensorchip, diverse kit och reagenser (förbrukningsartiklar) samt IFC (Mikroflödesceller) och Optiska interface (reservdel) som används vid analys av proteiner och molekyler med hjälp av Biacore instrument. Som processingenjör så har du processansvaret för produktionen a... Visa mer
Vi söker en processingenjör till sektionen Chip & IFC, inom Biacore consumables produktionen i Uppsala. Sektionen består av 1 chef, 2 ingenjörer och 14 operatörer. Tillverkningen består av Sensorchip, diverse kit och reagenser (förbrukningsartiklar) samt IFC (Mikroflödesceller) och Optiska interface (reservdel) som används vid analys av proteiner och molekyler med hjälp av Biacore instrument. Som processingenjör så har du processansvaret för produktionen av två viktiga komponenter till Biacore instrumenten, IFC (Mikroflödesceller) samt Optiska interface.
Tjänsten är ett föräldravikariat och gäller från och med 2020-05-11 till och med 2021-01-31.
Arbetsuppgifter
Rollen som processingenjör är varierande, stimulerande och utmanande där du kommer att supportera, följa upp och trenda den dagliga produktionen, hantera avvikelser och förbättringsärenden, medverka i införandet och kvalificering av ny utrustning och produkter i nära samarbete med Forskning och utvecklingsavdelningen, medverka vid felsökningar, ta fram och uppdatera tillverkningsmetoder, strukturer och dokumentation, utreda reklamationsärenden m.m. Produktionen sker som regel dagtid måndag till fredag.
Vidare kommer du att:
Följa produktionsutfall, uppmärksamma kvalitetsbrister och rapportera dessa i kvalitetssystem samt initiera och driva förbättringsåtgärder.
Stödja produktionspersonalen i det dagliga arbetet.
Driva och delta i förbättringsarbete och problemlösning inom processansvarsområdet.
Utbildning och upplärning av personal inom processansvarsområdet. Utarbeta underlag till att underhålla ORACLE-strukturer.
Upprätta och uppdatera tillverkningsdokument i olika system såsom Magic och MyWorkshop.
Förbereda och driva Change Control-ärenden.
Stödja reklamationsärenden och –utredningar.
Delta i och vid behov driva investeringsärenden. Samarbeta med F&U vid nyproduktprojekt och produktvårdsprojekt

Din bakgrund
Civilingenjör eller motsvarande med inriktning mot bioteknik/kemiteknik/maskinteknik eller liknande.
Goda kunskaper i svenska och engelska
God datorvana Förmåga att jobba i grupp och självständigt
God problemlösningsförmåga
Kunna se konsekvenserna av beslut eller aktivitet innan den genomförs
God noggrannhet och ordningssinne Kunna ta egna initiativ och fatta beslut
God förmåga att kunna driva flera aktiviteter samtidigt



Vi ser gärna att du har:
Intresse och erfarenhet av tillverkningsprocesser/produktionsutrustning
Erfarenhet från användning av Biacoreinstrument
God vana att arbeta i excel
Erfarenhet av att arbeta med förbättringsarbete med hjälp av t.ex. Lean metodik.
Har ledaregenskaper
Erfarenhet av av databaser (t.ex. Oracle, )
Vi söker dig som är engagerad och gärna arbetar i lag.
Du är tekniskt intresserad, lättlärd och inspireras av utmaningar!
Som person är du noggrann och mån om att alltid leverera rätt kvalitet till kunden. Visa mindre

Sourcing Specialist

Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing innova... Visa mer
Help us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.


What you'll do
The Sourcing Specialist Service Spare Parts will work closely with assigned Sourcing Leader for Service Spare parts as the local owner for assigned suppliers. These responsibilities include the execution of strategies to ensure realization of the business objectives within the Purchase Family.


Driving sourcing execution for assigned suppliers, including full accountability for meeting deflation targets
Monitoring supplier quality and delivery performance, developing improvement strategies to ensure business needs are met and working with suppliers to improve accordingly
Supporting NPIs and business with RFQ for new and existing items
Managing supplier data in ERP system, including setup of new items
Support in resolving customer complaints related to Service Spare Parts



Who you are
Bachelor’s Degree in Engineering technical discipline, business administration or supply chain, or relevant work experience
Some Commercial Sourcing or Supply Chain experience
Proficiency in the Microsoft Office package
Fully fluent in English (written and spoken)
Applicable work permit
Knowledge and understanding of Cytiva Purchasing Controls Procedure and associated Work Instructions and operates within them to ensure that all purchased product and services conform to specified requirements
Develop and maintaining of fully qualified and compliant supply base
Excellent communication and presentation skills with the ability to manage and develop supplier relationships
Ability to energize, develop and build rapport at all levels within an organization
Proven ability to execute and deliver on commitments
Analytical skills and experience from Excel
Experience from working in ERP system



Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.


Want to know more? Take a look at our Instagram, Twitter and LinkedIn pages! Visa mindre

Scientist/Senior Scientist

Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing inno... Visa mer
Help us improve access to life-changing therapies that can transform human health


We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.


What you'll do
We are looking for a Scientist/Senior Scientist to join the Bioprocess Application section within the R&D Downstream Resins department. The section is based in Uppsala and consists of about 10 biochemists and application specialists within the area of purification of viral vectors, recombinant proteins, plasma and monoclonal antibodies. The position is focused on the development of purification- and analysis methods for viral vectors such as AAV and lentiviruses. The position includes active participation in research and development projects where you will contribute with expertise within the field of viral vectors, in particular AAVs. You will be working in a team that is focused on developing and establishing efficient purification procedures for viral vectors using existing products or products under development. The position involves developing and establishing analytical methods typically used in the manufacturing and characterization of viral vectors, such as qPCR and, ELISA. In addition you will be participating in the evaluation of newly developed purification resins for viral vectors. You are also expected to identify, develop and maintain external networks within the field as well as act as activity leader of section activities within a project.


Who you are
Ph.D. degree in virology, analytical sciences, or related field
Technical knowledge and practical experience of the preparation of viral vectors or viruses is highly desirable
Proven ability of planning, executing and evaluating analytical & preparative experiments
Considerable knowledge and experience of Biotechnology/Biochemistry, experience from viral vectors or virology
Familiarity with analytical methods typically used in the manufacturing and characterization of viral vectors, e.g. ELISA, qPCR or ddPCR
Strong interest and skills in practical laboratory work
Scientific leadership skills
Excellent communication skills (both written and spoken), including presentation skills
Goal-oriented team worker
English as a working language
Experience of working with purification/downstream process of viral vectors, preferably AAV or lentivirus
Knowledge and experience with AAV biology
Fluent in Swedish



Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.


Want to know more? Take a look at our Instagram, Twitter and LinkedIn pages! Visa mindre

Custom Parts Specialist

Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing innova... Visa mer
Help us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.


What you'll do
The Custom Parts Specialist is responsible for driving world-class fulfillment of service spare parts transactions to enable high levels of customer (internal + external) satisfaction. Through strong collaboration with global supply chain, manufacturing sites, OEM/Suppliers, Global Services and Genpact.
In the custom parts team (CPT) we supply our customers through the service organization with non-regular spare parts.
The CPT member overlook and handle the whole chain from request to final delivery. Interact with suppliers and our experts for fast response to the service organization on customized spare parts
Customer focus from start to the end through the whole chain
Ensure regular communication updates around custom parts status to stakeholders/customers
Contribute to the development and improvement of the quoting process
Responsible for creating the format for all packaging material used for custom spare part deliveries



Who you are
Engineering degree from high school/engineering college or corresponding degree or equivalent knowledge or experience
Strong work experience
Proven project management or direct or indirect people leadership experience
Self-motivated, self-starter with the ability to work independently and learn quickly
Understand that the customers determine our success
Knowledge on engineering design principles, architectures and advancements in engineering concepts and technologies
Effective communication skills and boundless behavior—ability to present ideas and cases clearly and concisely
Experience of working in project teams meeting deadlines and deliverables
Fluent speaking and writing in English language
Applicable Work-Permit
Technical degree such as B Sc in Engineering or similar or equivalent knowledge or experience
Experience working in a Service or Systems Engineering team
Experience of PDMsystems (Magic)
Experience of defining requirement specifications
Proven ability to work cross functionally
Demonstrated supplier and manufacturing interface skills
Excellent communication, influencing skills and ability to gain buy-in for initiatives
Proven LEAN skills
Demonstrated problem-solving and leadership skills



Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.


Want to know more? Take a look at our Instagram, Twitter and LinkedIn pages! Visa mindre

DevOps Software Engineer

Dina huvuduppgifter som DevOps Software Engineer på Cytiva i Uppsala är att designa, implementera, underhålla och optimera den miljö som används för mjukvaruutveckling, byggnad och distribution. Utvecklingsmiljön är Windows-baserad. Du kommer att ingå i ett team som är huvudnavet för all programutveckling som sker på vår FoU-avdelning. Det betyder att teamarbete är viktigt eftersom utmaningar kommer från alla håll. Du och teamet hjälper varandra att underh... Visa mer
Dina huvuduppgifter som DevOps Software Engineer på Cytiva i Uppsala är att designa, implementera, underhålla och optimera den miljö som används för mjukvaruutveckling, byggnad och distribution. Utvecklingsmiljön är Windows-baserad. Du kommer att ingå i ett team som är huvudnavet för all programutveckling som sker på vår FoU-avdelning. Det betyder att teamarbete är viktigt eftersom utmaningar kommer från alla håll. Du och teamet hjälper varandra att underhålla och utveckla vår miljö så att utvecklarteamen kan bygga/testa/släppa ny programvara på ett effektivt sätt.
Vår avdelning utvecklar programvara som används av universitet och läkemedelsföretag för upptäckt och utveckling av biologiska läkemedel för att bekämpa sjukdomar som cancer och diabetes. Eftersom vår övergång till molnbaserade lösningar pågår kommer du att spela en viktig roll i denna övergång och ha möjlighet att påverka inriktning och slutresultat.


Arbetsuppgifter kommer i huvudsak bestå av: Drift, support och optimering av CI-miljön Cloud infrastruktur: automatisering, konfiguration och övervakning CI/CD: som en del av teamet utveckla och underhålla automatiska byggen, test och driftsättningar


Din bakgrund
Utmärkta kunskaper i svenska och engelska, både tal ock skrift
Examen i datavetenskap eller liknande
Några års erfarenhet från professionell programvaruutveckling (C # .NET och GIT)
Erfarenhet från DevOps-position Erfarenhet och kunskap i att arbeta i en smidig utvecklingsmiljö
Arbetstillstånd för EU



Desired Characteristics
Erfarenhet från att arbeta med Azure DevOps.
Intresse och erfarenhet från att utveckla och underhålla automatiska bygg- och smoketester.
Erfarenhet från automatiserad GUI-testning.
Att få saker att fungera smidigt, men samtidigt inse att verkligheten är allt annat än smidig hela tiden.
Att vara serviceinriktad och lösningsorienterad kommer definitivt att hjälpa till att utmärka sig i denna roll. Visa mindre

Produktionsingenjör

Vi söker en Produktionsingenjör till sektionen Kolonnproduktion, som är en del av den kemiska produktionen inom GE Healthcare i Uppsala. Sektionen består av 20 personer och producerar kromatografikolonner av olika storlekar (montering, fyllning, testning, förpackning och granskning/frisläppning). Produktionsingenjören vi söker kommer främst att höra till produktion av kolonner för användning i processkala, vilket är ett starkt växande och spännande område.... Visa mer
Vi söker en Produktionsingenjör till sektionen Kolonnproduktion, som är en del av den kemiska produktionen inom GE Healthcare i Uppsala. Sektionen består av 20 personer och producerar kromatografikolonner av olika storlekar (montering, fyllning, testning, förpackning och granskning/frisläppning). Produktionsingenjören vi söker kommer främst att höra till produktion av kolonner för användning i processkala, vilket är ett starkt växande och spännande område. Tjänsten är tillsvidare.
Arbetsuppgifter
Jobbet som produktionsingenjör innebär framför allt att vara ett dagligt stöd till produktionen. Rent praktiskt innebär det i stora drag:
avvikelsehantering, felsökning av processutrustning, kontakter med UH och/eller entreprenörer.
Du driver även igenom förbättringsförslag och ChangeControl-ärenden, uppdaterar produktionsdokument samt utför och dokumenterar riskanalyser mm.
Representera produktionsavsnittet vid audit.
Följa produktionsutfall, uppmärksamma kvalitetsbrister och rapportera dessa i kvalitetssystem samt initiera och driva åtgärder för dessa inom ramen för processansvar.
Stödja produktionspersonalen i det dagliga arbetet.
Delta i processvårdsprojekt samt driva upp- och nedskalning och flytt av processer och produktionsutrustning.
Driva och delta i förbättringsarbete och problemlösning inom processansvarsområdet.
Utbildning och upplärning av personal inom processansvarsområdet.
Utarbeta underlag till att underhålla ORACLE-strukturer.
Upprätta och uppdatera tillverkningsdokument i olika system.
Förbereda och driva CC-ärenden. Stödja reklamationsärenden och –utredningar.
Delta i och vid behov driva investeringsärenden.
Samarbeta med F&U vid nyproduktprojekt och produktvårdsprojekt.
Beställa/implementera ny utrustning och utföra kalibreringar.
Analysera produktionsutfall Hålla i processforum.
En del av sektionens tillverkning sker i renrum. Så i rollen kommer det att ingå arbete för att säkerställa att renrummet håller sin klass.



Din bakgrund
Civilingenjör eller motsvarande med inriktning mot bioteknik/kemiteknik/maskinteknik eller liknande.
Du behärskar svenska flytande i tal och skrift och har god kommunikationsförmåga.
Du behärskar engelska i tal och skrift
Erfarenhet av processindustri och/eller god labvana
God datorvana
Förmåga att jobba i grupp och självständigt
God problemlösningsförmåga
Kunna se konsekvenserna av beslut eller aktivitet innan den genomförs
God noggrannhet och ordningssinne Kunna ta egna initiativ och fatta beslut
God förmåga att kunna driva flera aktiviteter samtidigt Desired



Characteristics
Intresse för tillverkningsprocesser/produktionsutrustning
Tidigare erfarenheter samordning/planering.
Kunskaper om Six Sigma
God vana att arbeta i excel
Erfarenhet av LEAN och dess verktyg Visa mindre

Project Assistant

Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of Cytiva, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative ... Visa mer
Help us improve access to life-changing therapies that can transform human health


We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of Cytiva, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.


What you'll do


Are you planning on taking a “sabbatsår” – this could be the perfect opportunity. We are searching for a Project Assistant with media profile for a one year assignment part time (50%).


We are a team in the Product Management organisation in BioProcess Downstream called the Operations team. The team drives, coordinates and supports business processes that spans across the BioProcess Downstream portfolio, covering things like life cycle management, strategy, pricing, product training and quality. This position will primarily provide coordination support of different product training events and other type of communications such as short video messages. Typical tasks include video recording and editing, coordination of small teams driving event planning, ensuring that tasks are completed on time by each team member. Event planning could include planning and running internal conferences hosted on local site in Uppsala. The position also includes layout using Word, Powerpoint and Excel. It can also extend to supporting other administrative tasks using our internal tools, e.g. for ordering. Additional support to the Product Management organization will also be part of this role. These tasks may be adapted to the profile and interests of the successful candidate. This is an entry-level position.
Video recording
Video editing
Coordination with people on smaller activities
Supporting, coming up with ideas and following up on planned activities when planning events such as internal conferences
Layout fix in word, pptx and excel
Administration of excel lists
Communication and interaction with Product Management, Marketing organisation, and the Communications team
Open minded to support with everything



Who you are
Gymnasieutbildning
Proficiency in video editing and recording
Organisational skills; able to coordinate small teams to drive activities
Proficiency in using Word, Power Point software and Excel
Proficiency in English
Strong oral and written communication skills
Outward and social, not afraid of reaching out to people and making new connections
EU workpermit is requied Visa mindre

Production Planner

Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing innova... Visa mer
Help us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.


What you'll do
Production planner within the chemical production site in Uppsala. The role means planning production and managing service level of finished goods as well as maintain inventory at agreed levels this is done in close cooperation with production departments and distribution planners.
Maintain production plan and utilize plant capacity
Lead planning meetings
Inventory management
Allocation of material
Process improvement work

Who you are
Technical or Economical upper secondary school and some experience from manufacturing industry
Apics or equivalent Production planning training
Experience from ERP- systems as well as skills in Excel
Sense of responsibility combined with a service minded attitude
Communication skills in both English and Swedish
Well developed leadership skills and ability to engage and inspire others
You need experiences of working in complex environments with many internal contacts
You will need both interpersonal and administrative skills to be able to maintain an accurate plan and work closely together with production and distribution
You will have to have an ability to learn fast and work with some degree of uncertainty



Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.


Want to know more? Take a look at our Instagram, Twitter and LinkedIn pages! Visa mindre

Styr- och reglertekniker

Sektionen MAINTENANCE söker en Styr och Reglertekniker till underhållsavdelningen som är en del av kemisk produktion inom GE Healthcare i Uppsala. Vår sektion består av 18 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. Arbetsup... Visa mer
Sektionen MAINTENANCE söker en Styr och Reglertekniker till underhållsavdelningen som är en del av kemisk produktion inom GE Healthcare i Uppsala. Vår sektion består av 18 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.
Arbetsuppgifter:
Kalibrering av mätinstrument som ligger inom ramen för sektionens ansvar.
I och ur koppling av elektriska processutrustningar. Felsökning på processutrustningar.
Förebyggande och avhjälpande underhåll av processutrustningar.
Medverka vid genomförande, uppföljning och underhåll av system för fortlöpande tillsyn.
Medverka vid utveckling, implementering och uppföljning av system för utvärdering av underhållsarbetets effektivitet. Jourberedskap var 6:e vecka torsdag till torsdag enligt lokalt avtal.

Din erfarenhet
Treårig gymnasieutbildning med styr- och reglerteknik, elektronik och El, Alt Teknikprogrammet.
Brett tekniskt intresse
Goda kunskaper inom automationsområden som styr- och reglerteknik, mekanik, elektronik, hydraulik och pneumatik samt datorteknik.
Goda kunskaper inom område processteknisk utrustning
Kunskaper inom CAD området Electrical
Kunskap inom området PLC-programmering



Vid eventuella frågor, vänligen kontakta rekryterande chef Martin Frick 018-6120393. Visa mindre

BioPharma Indirect Sourcing Leader

Role Summary: The Indirect Sourcing Leader will be the key point of contact for sourcing activities in the Logistics Category. The role will report directly to the Biopharma Sourcing Manager for Logistics and be a key member of the Indirect sourcing team to ensure global strategies are developed and deployed in partnership with the business stakeholders. Essential Responsibilities: In this role, the Indirect Sourcing Leader will take the lead for sourcing ... Visa mer
Role Summary:
The Indirect Sourcing Leader will be the key point of contact for sourcing activities in the Logistics Category. The role will report directly to the Biopharma Sourcing Manager for Logistics and be a key member of the Indirect sourcing team to ensure global strategies are developed and deployed in partnership with the business stakeholders.
Essential Responsibilities:
In this role, the Indirect Sourcing Leader will take the lead for sourcing activities in the regions, to ensure the business have the right partners both from a cost, quality and business growth perspective.


• Be a key partner to the business on matters related to sourcing activites in the Logistics category, covering freight, warehousing, packaging and brokerage.
• Provide sourcing leadership and support to stakeholders at all levels of the organization in the effort of building a strong partnership with key suppliers.
• Be the subject matter expert on the supply chain marked conditions, latest trends, innovation and cost control. Warehousing experience highly desired.
• Lead and drive the sourcing process from RFP, RFQ and contract development.
• Lead regular sourcing reviews with internal stakeholders and external suppliers.
• Faclitate cross-functional workouts and efforts as related to sourcing processes, procedures and related cost improvements.
• Support internal stakeholders on business growth and expansion plans.
• Build strategic sourcing road maps based on business growth and customers needs.
• Drive Simplification projects on sourcing processes and tools.
• Conduct training on sourcing processes and serve as key point of contact on sourcing inquiries.
• Drive sourcing process compliance; Provide input to, and support of procedures and guidelines as necessary.


Qualifications/Requirements:
• MCIPS or equivalent Professional Procurement qualification, or BA or BS degree or other advanced degree in Supply Chain, Purchasing, Economics or equivalent.
• At least 5 years of experience in Sourcing, Project Management, Finance, or Logistics Operations.
• Excellent interpersonal communications and negotiation skills with ability to influence at all levels of the organization.
• Strong analytical skills, BI development and database management skills.
• Strong communication (verbal, written & presentation); skilled in working collaboratively with remote personnel.
• Self starter who can work independently with key stakeholders at all levels of the organization.
• Strong Project management & process improvement skills.
• Applicable work permit


Desired Characteristics:
• Fluent English both verbal and written. 2nd language preferred.
• Green or Black Belt certified/ Lean experience.
• Excellent communication skills.
• Experience with Oracle, TMS, WMS, Qlick or other relevant BI and purchasing tools.
• Experience leading simplification projects.
• Experience in the logistics industry.
• Experience with divestitures. Visa mindre

Global Product Manager Filtration HW

Role Summary: Summary: We are searching for a commercially experienced Global Product Manager to join the BioProcess standard Downstream Hardware team. Your main responsibility will be to manage the Filtration hardware portfolio, a growing part of the BioProcess Hardware business. You will develop strategies and tactical execution plans for the products in order to maximize sales and profitability over the products' life cycle. Essential Responsibilities... Visa mer
Role Summary:
Summary: We are searching for a commercially experienced Global Product Manager to join the BioProcess standard Downstream Hardware team. Your main responsibility will be to manage the Filtration hardware portfolio, a growing part of the BioProcess Hardware business. You will develop strategies and tactical execution plans for the products in order to maximize sales and profitability over the products' life cycle.


Essential Responsibilities:


Key aspects of the role include:


Represent customer interests for your product(s) inside GE. Ensuring customer focus by building rapport with customers as required and ensuring the "voice of the customer" is reflected in work processes
Develop a product life cycle strategy and recommend investment and NPI development. Manage all aspects of the product(s)' life cycle including pricing, marketing and supply chain related recommendations
Drive the overall product development process for NPIs. Create business cases and adjust/monitor before and during product development and launch. Prepare and implement product launch plans, coordinating with commercial stakeholders to define go-to-market strategy
Define and recommend value engineering of products redesign to extend life cycle. Provide input and prioritization to R&D and Supply chain on requirements for support, product care and research & development projects, including customizations
In close collaboration with other product managers, R&D and Service make sure that the product strategies are in-line with business priorities in adjacent areas such as filtration consumables and automation
Ensure targets for production cost, inventory levels and quality are met. Provide leadership to Quality, Sourcing and Supply Chain functions to ensure the portfolio retains and improves upon its position in these areas
Provide sales and profitability forecasts to internal stakeholders
Support commercial organisation with marketing material and sales tools
Coordinating the needs across a multi-functional organization, including marketing, sales, operations, engineering, and services teams, while ensuring compliance with quality systems and regulatory requirements
Close collaboration with marketing to translate practice needs, market analysis, competitive analysis, and regulatory environment factors into actionable strategies and tactics for the product
Own the pricing strategy and its implementation for your product(s)
Ensure product readiness for sale and use. Manage such things as product registration, labelling, legal and safety requirements, storage conditions, logistics, technical content of databases, and after sales support together w Service



For more information please contact Kristina Uhlen +46 706120838 [email protected]


Qualifications/Requirements:


Bachelor’s Degree in Engineering/Life Sciences/Biotechnology
Proven experience in a Life Sciences based business, including experience in marketing, sales, or product management
Major experience in Process science or related field including workflow experience with similar products
Experience of customer/market focused activities
Strong business and technical acumen
Good interpersonal and communication skills, plus experience of using these skills to participate in and influence cross-functional teams
Ability to work effectively in a matrix environment
For work in Sweden EU work permit is required



Desired Characteristics:


Sales experience
Marketing Diploma or equivalent
Awareness of GEHC product portfolio that serves this market
Good understanding of the filtration technologies and applications
Good understanding of the biopharmaceutical manufacturing environment and the needs of the customers in this market
Proven ability and expertise in working to combine hardware and automation with a customer focused mindset
Team oriented
Ability to motivate and work well with diverse, cross-functional teams
Operates in a goal-oriented way with proven personal drive and delivery performance Visa mindre

Global Bioprocess Financial Planning & Analysis Specialist

Role Summary: The Global Bioprocess FP&A Specialist provides financial planning and analysis leadership for the Global Bioprocess business within GE Healthcare Life Sciences Biopharma. Ideally suited to candidates with prior FP&A experience and offers an opportunity to further develop in a high growth and dynamic global business with ~$3BN revenue. Essential Responsibilities: Develop quality, provocative and efficient sales to operating profit business i... Visa mer
Role Summary:
The Global Bioprocess FP&A Specialist provides financial planning and analysis leadership for the Global Bioprocess business within GE Healthcare Life Sciences Biopharma. Ideally suited to candidates with prior FP&A experience and offers an opportunity to further develop in a high growth and dynamic global business with ~$3BN revenue.


Essential Responsibilities:
Develop quality, provocative and efficient sales to operating profit business intelligence across regions, products and functions. Develop relevant exec reporting for CFO, CEO and direct staff members
Evaluate key business drivers including FX and headcount. Track progress against plans at a granular level. Details variance drivers. Identify root causes and recommend actions to get to planned performance for the operating teams.
Responsible for monthly operating reviews with the Life Sciences CEO and CFO. Lead the preparation of the financial submissions, deck, cribs and relevant storytelling.
Identifying risks & opportunities during each quarter and leading team in mitigating risks and capitalizing on opportunities
Responsible for quarterly closing/estimates and develop reliable estimates of sales to operating margin; communicate current results and estimates to business leaders.
Leading planning cycles including developing estimates, operating plans/forecasts/reviews, Blueprint Reviews (BPR) (2-year plan); OP (operating plan/budget) and / or corporate reporting.
Work closely with the Bioprocess GM and CFO on all aspects of financial analysis, planning
Support Regional Finance Managers and Business Leaders to understand & drive opportunities for Growth and managing cost. Lead and provide analytics on strategic initiatives
Driving standardization, process improvement and simplification across operating businesses in all aspects of planning and reporting, including best practice sharing



For more information about the position please contact Jens Kristianson +46 737286916 [email protected]


Qualifications/Requirements:


Bachelor’s Degree in Accounting, Finance, Economics, or Business Administration and strong financial work experience; OR high school diploma / GED and strong progressive financial work experience / or equivalent knowledge or experience
EU work permit



Desired Characteristics:
Analytic and commercial skills: able to clearly link financial results to operational performance drivers, generate alternatives and drive positive change
Clear thinking / problem solving: able to quickly grasp new ideas Visa mindre

Finance Specialist - FP&A Operations

Role Summary: The FP&A Finance Analyst is a key member of the FP&A team of the Bioprocess business within GE Healthcare Life Sciences Biopharma. The role manages the main processes & tools for the FP&A cycle such as reporting, closing & planning. This is dynamic finance role which is a perfect fit for a recent university student with a major in Finance or someone with first years of experience who is interested in joining a global and successful business ... Visa mer
Role Summary:
The FP&A Finance Analyst is a key member of the FP&A team of the Bioprocess business within GE Healthcare Life Sciences Biopharma. The role manages the main processes & tools for the FP&A cycle such as reporting, closing & planning. This is dynamic finance role which is a perfect fit for a recent university student with a major in Finance or someone with first years of experience who is interested in joining a global and successful business


Essential Responsibilities:
Timely support of global BP forecasting and reporting requirements such as monthly estimates, closing & planning processes
Commercial FP&A – funnel, backlog & orders reporting, trending & forecasting
Manage Bioprocess HQ cost with forecast, reporting & business partnering
Deliver on identified business simplification / initiatives and cross-functional projects/process improvement within operations/finance function
Commercial metrics reporting
Support Regional Finance Managers and Business Leaders to understand & drive opportunities for Growth and managing cost
Driving standardization, process improvement and simplification across operating businesses in all aspects of planning and reporting



For more information about the position please contact Jens Kristianson +46 737286916 [email protected]


Qualifications/Requirements:
Bachelor’s degree in Accounting, Finance, Economics or Business Administration or equivalent knowledge or experience
Working experience within Finance is an advantage, but not a must for this role
EU work permit



Desired Characteristics:
Analytic and commercial skills: able to clearly link financial results to operational performance drivers, generate alternatives and drive positive change
Clear thinking / problem solving: able to quickly grasp new ideas
Communication skills: able to clearly communicate financial information in an easy to understand manner; able to deliver message effectively verbally and in writing
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
Integrity: Accepting and adhering to high moral, ethical, and personal values in decisions, communications, actions, and when dealing with others
Solid PC skills: experience with financial systems/applications, strong Excel skills in data compilation and aggregation and proficiency in Power Point
Fluency in English, knowledge of Swedish is an advantage Visa mindre

Product Manager Microcarriers

Role Summary: This role provides multi-functional leadership and strategic direction for GE’s Microcarrier portfolio including the Cytodex and Cytodex Gamma brands. You will own the portfolio from product roadmap to organization readiness and product/service delivery. Essential Responsibilities: Working collaboratively with commercial teams, supply chain, R&D and other functions to drive revenue and profitability of the business. Additionally, this... Visa mer
Role Summary:


This role provides multi-functional leadership and strategic direction for GE’s Microcarrier portfolio including the Cytodex and Cytodex Gamma brands. You will own the portfolio from product roadmap to organization readiness and product/service delivery.


Essential Responsibilities:


Working collaboratively with commercial teams, supply chain, R&D and other functions to drive revenue and profitability of the business.


Additionally, this position will focus on evaluating our existing portfolio and developing organic and inorganic strategies to expand and drive incremental growth. This will require leadership through influence and participation in key business decision making forums such as R&D Portfolio, Product Care, Product Quality, and Sales & Operations planning.




Management of the Microcarrier portfolio over its life cycle within a product portfolio of a business area in a manner that maximizes the overall return/profit to the company, within the context of company, business area and marketing plans. Ensures compliance with quality systems, regulatory requirements, and commercial change process.
Manages all aspects of the product(s) life cycle starting with the detailed planning phase until the product is terminated. Define Product Models, Offerings and Structures.
Develop strong cross functional relationships with Supply Chain, R&D, Quality, Sourcing and other key functions to successfully drive both short-term and long-term projects to strengthen product offerings.
Partner with marketing to create compelling customer facing material, and commercial sales tools.
Maintain customer focus on value of Microcarrier products. Represent voice of customer internally to advocate for customer needs.
Establish and maintain strong working relationships with commercial team members including account managers and modality experts.
Become a product/business expert in Microcarriers. Function as the point of contact for questions and problem solving for internal business partners and external customers.
Support the establishment/refinement of product management processes, including annual road-mapping and pricing review.
Identify market trends and opportunities in the Bioprocess Microcarrier landscape.



Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


For more information about the position please contact Jon Van Pelt [email protected] or +1 508 683 3745


Qualifications/Requirements:


Bachelor’s Degree in Marketing, Engineering, Science, Business Administration or related field or equivalent knowledge or experience.
Extensive experience in product marketing, product development, or related field.
Product Management/Marketing expertise, including: market trends/analysis, NPI process, product roadmap development, product life-cycle management.
Excellent oral and written communications skills in English. Swedish also an advantage.
Strong analytical and process skills.
Strong project management skills.
Ability to work effectively within a matrix environment



EU Work permit Visa mindre

Custom and Lab filtration Specialist Nordics/BeNeLux

Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing in... Visa mer
Help us improve access to life-changing therapies that can transform human health


We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.


Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.


What you’ll do


As the Custom and Lab Filtration Specialist you’ll generate new and reoccurring business for standard and custom ranges within the Nordic/BeNeLux region with our biotech, academic, pharma and industrial customers.


Build end user demand for both direct and indirect customers and spend at least 70% of time in the field.
Motivate, encourage and support distributors to promote Lab filtration ranges in named key accounts .
Partner with the Consumable Sales Specialist to implement the direct and indirect strategy for Lab Filtration.
Negotiate sales and deal closures, influencing key decision makers.
Use Salesforce.com to forecast and monitor business and to ensure transparency to total customer engagement.



Who you are


Have strong consultative sales experience; experience working with distributors preferred
Understand applications of filtration products
Strong analytical skills with the ability to review customer data and develop financially sound sales solutions
Excellent communicator able to synthesize complex issues into simple messages
Fluent in English (written and verbal)
Earned a Bachelor’s degree or the equivalent, preferably in the life sciences
Possess a valid motor vehicle license and willing to travel within the region with occasional overnight stays Visa mindre

Field Service Sales Specialist - Nordic Region

Role Summary: TIn this role you will grow service Sales in the Nordic region through creating and maintaining long term customer relationships/satisfaction. Prospect, Qualifies, quotes and closes new GE Life Sciences service opportunities. Visits Pharmaceuticals, Biotech and Academia customers to nurture the contract business and develop other service products. Essential Responsibilities: The job is field based (either in Sweden or Denmark) and will requ... Visa mer
Role Summary:
TIn this role you will grow service Sales in the Nordic region through creating and maintaining long term customer relationships/satisfaction. Prospect, Qualifies, quotes and closes new GE Life Sciences service opportunities. Visits Pharmaceuticals, Biotech and Academia customers to nurture the contract business and develop other service products.


Essential Responsibilities:
The job is field based (either in Sweden or Denmark) and will require to work closely with other channels in the GE Healthcare Life Science organization to develop and implement a sales plan and targeted account strategies that will meet/exceed sales quotas.


Main duties to include but may not be limited to will be;
· Act as primary salesperson for service sales opportunities in the Nordic region
· Develop and implement commercial service strategy and action plan for your assigned region
· Partner with other GE Life Sciences field sales and service personnel in their efforts to sell strategic offerings and maximize account penetration
· Prospect, qualifies, quotes and closes new GE Life Sciences service opportunities
· Implement a targeted and proactive visit/call schedule to ensure customer service contracts are renewed and increase service sales growth
· Maintain records of account history, contacts and current and long-term service purchase plans
· Develop competitive product knowledge, and clear understanding of market dynamics in order to offer creative solutions to customers
· Monitor sales development according to key performance indicators in place


Qualifications/Requirements:


Must speak English and Danish and/or Swedish in order to communicate with regional customer base and GE internal organisation


· Willingness to travel regularly according to business needs (min 50% of your time)


· University degree in Biosciences/Biotechnology
and/or business.


· Demonstration of at least one of the following core sales experiences in the Healthcare and/or Life science service industry: external direct sales or over the phone business to business sales


· Proven track record of sales success including: developing, organising and implementing sales plans; meeting and exceeding sales targets; penetrating new accounts through proficiency in prospecting, lead qualification, sales and negotiations.


· Demonstrate excellence in ability to interact effectively with all levels of an organisation, both internally and with external customers.


· This position requires a high degree of self-motivation and prioritization skills. The ideal
candidate f/m must also have a talent for getting along with and working productively with a variety of highly motivated sales personalities in a matrix environment Visa mindre

Customer Case Management Engineer - Software department

Role Summary: The BioProcess Software department develops software for systems helping our customers in the pharma industry and universities to invent and develop biological medicines for diseases such as cancer and diabetes. We are now looking for two Customer Case Management (CCM) Engineers to join the BioProcess Software department within BioProcess R&D (Research and Development) at our site in Uppsala. Essential Responsibilities: As a Customer Case... Visa mer
Role Summary:


The BioProcess Software department develops software for systems helping our customers in the pharma industry and universities to invent and develop biological medicines for diseases such as cancer and diabetes.


We are now looking for two Customer Case Management (CCM) Engineers to join the BioProcess Software department within BioProcess R&D (Research and Development) at our site in Uppsala.
Essential Responsibilities:
As a Customer Case Management (CCM) Engineer in the BioProcess SW department within BioProcess R&D, you will be responsible for the customer case management for software products. The CCM Engineer coordinates, prepares, and resolves customer cases in collaboration with software and system engineers, and provides support to field service engineers, the customer support office, and our customers around the globe. You will be based in Uppsala and work in a global environment where your language skills and interest for different cultures will be of great value.


In this role you will be part of a small team, building, and developing the customer case management function within the department. Being service minded and solution oriented is key to excel in this role.


Essential responsibilities:
Develop a strong working relationship with the teams in the BioProcess SW and System departments and the service organization, ensuring effective communication
Acting as a subject-matter expert in our SW products
Support field service engineers and the customer support office, providing technical knowledge about IT, database infrastructure configurations, and general technical knowledge about our software products and systems
Investigate customer cases related to our SW products in collaboration with SW and system engineers within R&D
Plan, prioritize, and drive work items
Be part of building, developing, and driving the CCM team
Develop and refine our work processes for CCM
Communicate with customers and internal stakeholders both written and orally
Document technical investigation results
Support development of new products and maintenance of legacy products during testing periods, and planning



For questions, please contact hiring managers:
Anders Wessman, tel. +46 (0)73-036 30 12 or [email protected]
Ulrika Öhman, tel. +46 (0)76-496 06 55 or [email protected]



Qualifications/Requirements:
BSc or equivalent
Fluent in English, written and spoken is required. Very good Swedish language knowledge
Excellent written and verbal communication skills
Ability to plan, coordinate, prioritize, and drive your work items
Technical interest in HW and SW
Interest in interacting with other people
Good problem-solving skills
Service minded
Skilled in computer networks and database installations
Enjoy working in an international environment
EU Work permit is required



Desired Characteristics:
Application knowledge within biotechnology and chemistry
Few years of experience in SW development (C # .NET)
Experience of working with lab equipment
Previous experience as a field service engineer or similar position Visa mindre

Section Manager Software Engineering

Role Summary: We are looking for a Section Manager for the SW Engineering section, which reports into the BioProcess Software Department within BioProcess R&D. The BioProcess Software department consists of approximately 65 persons divided into 4 sections and is responsible for Software development in the BioProcess downstream area. Examples of SW that we develop are UNICORN and Biacore SW. Essential Responsibilities: The SW Engineering section has four ... Visa mer
Role Summary:
We are looking for a Section Manager for the SW Engineering section, which reports into the BioProcess Software Department within BioProcess R&D. The BioProcess Software department consists of approximately 65 persons divided into 4 sections and is responsible for Software development in the BioProcess downstream area. Examples of SW that we develop are UNICORN and Biacore SW.


Essential Responsibilities:
The SW Engineering section has four essential responsibilities:
Driving the test and quality assurance strategy to improve efficiency in the development process
Perform Software Test and Quality Assurance for software releases
Perform release activities (configuration management/DevOps) for the software platforms
Software development for the UNICORN and Biacore software platforms



The section manager role includes management of the section and coaching/supporting section members. The section manager should also actively participate in the Software department Management Team and closely collaborate with project/program managers reporting to the Portfolio as well as with colleagues within and outside the department. As a section manager you will be accountable for securing deliverables from the section into the projects, fulfilling the section/department goals. You will work to continuously develop technical platforms, processes and people to secure delivery and quality of the products in an efficient way as well as continuously stimulate, develop and grow the employees in your team.


Responsibilities:
Drive the test and quality assurance strategy to improve efficiency in the development process.
To continuously enhance the working practices within the domain of responsibility, including training of personnel, recruitment's, process improvements, new tools, new external collaborations and networking.
To continuously monitor and work to improve the productivity of the section and the ability to deliver on time and budget.
Review and support project work when requested by processes, project manager or whenever needed by other reasons.
To maximize overall productivity and quality for all projects by allocating resources from the section to projects in the most optimal way based on overall priorities.
In collaboration with project manager appoint activity leaders in projects.
Authority to approve design input-, verification and design output documents.
Within assigned domain of expertise, decide in technical concept and drive to resolve technical impediments in projects, within framework given by project.



For questions, please contact Hiring Manager Åsa Nordstedt: tel. +46 (0)70 343 95 16 or [email protected]


Qualifications/Requirements:
MSc or similar education in the software area +/or equivalent knowledge or experience
Strong experience in relevant product development
Proven leadership and people management skills from e.g. line management or project management
Strong collaboration skills
Genuine interest in developing people and technical solutions
Strong communications skills
Fluent in Swedish and English, both verbally and in writing



Desired Characteristics:
Line management experience from agile SW development (agile/servant leadership) is highly desired
Knowledge & experience from SW development
Knowledge & experience from driving DevOps and/or CI/CD improvements Visa mindre

Sr Process- & Systems Manager

Role Summary: The PLM function has responsibility for Biopharma business systems such as: MAGIC, xCAD, Configurator, eLabNoteBOOK, SDL-Tridion Docs & ChemMate. Business systems ownership including associated budget responsibility. Accountable for process- and system governance for above mentioned enterprise platforms. Working with Biopharma business and IT to ensure strategic, tactical and operational alignment. Essential Responsibilities: Responsible fo... Visa mer
Role Summary:
The PLM function has responsibility for Biopharma business systems such as: MAGIC, xCAD, Configurator, eLabNoteBOOK, SDL-Tridion Docs & ChemMate. Business systems ownership including associated budget responsibility. Accountable for process- and system governance for above mentioned enterprise platforms. Working with Biopharma business and IT to ensure strategic, tactical and operational alignment.


Essential Responsibilities:
Responsible for developing processes (mainly design related) and associated system capabilities (mainly MAGIC) to maximize productivity, whilst ensuring compliance, scalability/growth and alignment with overall Biopharma priorities
Support relevant Biopharma businesses and functions with translation of their needs and requirements into program- and jobjar requests to be delivered by IT
Drive/enforce process standardization and product modularization to enable growth and ultimately improve
Through effective global and horizontal teamwork/collaboration, develop and drive continuous improvement of engineering processes (mainly design- and variant management) and associated system capabilities to maximize productivity, whilst ensuring compliance, scalability/growth and alignment with overall Biopharma priorities.
Drive/enforce process standardization, improve system architecture and product modularization to enable growth & ultimately improve outcome for our customers and the Biopharma business
Ensuring integration principles and requirements in Biopharma’s global eco system are met.
Translate business needs and functional requirements into enhancement requests to be delivered by IT (or Cloud/SaaS vendors).
Global UC Chairman for Engineering- & Variant Management and be active in the global Governance Board (? MAGIC platform) (may also include active participation in other User Councils)



Qualifications/Requirements:
BSc degree in Engineering/Technology or related field / or equivalent knowledge or experience
Relevant (product development) and / or industrial experience
Leadership experience as project or program manager
Excellent written and verbal communication skills; fluent in English (oral and written)
Solid knowledge of Product Modularization concepts
Familiar with LEAN principles
Proficient in Microsoft Office applications (i.e. Word, Excel and Powerpoint)



Desired Characteristics:
MSc or MBA degree
Major experience from standardization, process- and systems improvements
Deep knowledge/Extensive experience of Product Modularization
Skilled Lean Leader/Facilitator
Broad network and understanding of various functions, roles and processes in the Biopharma organization
Proven business/financial acumen, including demonstrated ability to motivate, influence, solve complex problems and drive change at all levels of the (matrix)organization.
Proven ability to work with cross-functional, multi-cultural teams and deliver results in an ambiguous-, dynamic- and multi-stakeholder environment
Strong communication, interpersonal, analytical and problem-solving skills
Skilled Coach, Influencer and Change Agent
Willing to travel up to 20% of your time domestically and internationally Visa mindre

Senior Technical Project Manager

Role Summary: We are looking for a Senior Technical Project Manager to work in the team managing Capital Expenditure projects. You will report to the Senior Manager Project Management Office. Essential Responsibilities: The Project department includes 16 persons working to support the GE site with management of investment projects to meet capacity and regulations requirements at Site Uppsala. The team consists of Sr Project Managers, Project Managers, Pr... Visa mer
Role Summary:
We are looking for a Senior Technical Project Manager to work in the team managing Capital Expenditure projects. You will report to the Senior Manager Project Management Office.


Essential Responsibilities:
The Project department includes 16 persons working to support the GE site with management of investment projects to meet capacity and regulations requirements at Site Uppsala. The team consists of Sr Project Managers, Project Managers, Project Engineers, Admin support and Purchaser.


As a Senior Technical Project Manager you will be responsible for the development, planning and building of our future Capital Expenditure projects. Your tasks will include developing ideas from the concept phase until the end of the implementation phase.
Your job is to develop project drafts, business cases in close collaboration with the internal stakeholders and to run feasibility studies.
You will collect ideas and solutions from different suppliers as well as collect budget offers for cost estimates.



The Senior Project Manager is responsible for managing large projects or a program of several projects. you will work across multiple functional areas to coordinate, collaborate and drive delivery of all projects within the project or program. Work results have a significant impact to the business.


Lead the execution of medium-size to large and complex projects and programs and ensure that all related activities are performed in accordance with the GE policy, contractual agreements, quality standards, environment, health, safety requirements, financial targets, as well as schedule commitments.
Leads the project team, establishes the project execution approach and oversees project hand-over, execution planning, and monitoring and control activities for both internal and external resources to accomplish all project goals.
Coaching and mentor Project Managers or the engineers in the line organization in tasks related to Project Management
Providing clear and timely communication regarding the status of the project/program – schedule, budget, progress to date, risks etc. to relevant stakeholders



Qualifications/Requirements:
Significant project/program management experience .
Excellent communications, conflict management and interpersonal skills
B.S./B.A./M.S. degree or equivalent technical training
Experience from managing projects in a global setting within an international company structure
Fluent in Swedish and English



For more information please contact recruiting manager Petra Olsson +46730598147 or [email protected] Visa mindre

Production Planner

Production planner within the chemical production site in Uppsala The role means planning production and managing service level of finished goods as well as maintain inventory at agreed levels this is done in close cooperation with production departments and distribution planners. Essential Responsibilities: Maintain production plan and utilize plant capacity Lead planning meetings Inventory management Allocation of material Process improvement work Q... Visa mer
Production planner within the chemical production site in Uppsala
The role means planning production and managing service level of finished goods as well as maintain inventory at agreed levels this is done in close cooperation with production departments and distribution planners.


Essential Responsibilities:
Maintain production plan and utilize plant capacity
Lead planning meetings
Inventory management
Allocation of material
Process improvement work



Qualifications/Requirements:
Technical or Economical upper secondary school and some experience from manufacturing industry
Apics or equivalent Production planning training
Experience from ERP- systems as well as skills in Excel
Sense of responsibility combined with a service minded attitude
Communicational skills in both English and Swedish



Desired Characteristics:
You need experiences of working in complex environments with many internal contacts. You will need both interpersonal and administrative skills to be able to maintain an accurate plan and work closely together with production and distribution. You will have to have an ability to learn fast and work with some degree of uncertainty. Visa mindre

Software Test Engineer/SQA Engineer

Vi söker en Software Test Engineer/SQA Engineer till vårt globala team som utvecklar applikationsmjukvara, webb- och klientserverbaserad, för framtagning och produktion av framtidens biologiska mediciner. Huvudsakliga arbetsuppgifter: Designa, genomföra och underhålla manuella och automatiserade testfall Sätta upp och underhålla testmiljöer och integrationer (system, operativsystem, webbläsaruppdateringar) Bidra till testarkitektur och process, både manu... Visa mer
Vi söker en Software Test Engineer/SQA Engineer till vårt globala team som utvecklar applikationsmjukvara, webb- och klientserverbaserad, för framtagning och produktion av framtidens biologiska mediciner.


Huvudsakliga arbetsuppgifter:
Designa, genomföra och underhålla manuella och automatiserade testfall
Sätta upp och underhålla testmiljöer och integrationer (system, operativsystem, webbläsaruppdateringar)
Bidra till testarkitektur och process, både manuell och automatiserad testning
Vara ansvarig för kvalitet, testanalys och testmetodik för programvaruprodukter
Vara testdelen i 3 Amigos och bidra till framgången för den utvecklade funktionen och arbetsflödet, t.ex. genom manuell och automatiserad testning. Detta inkluderar identifiering, analys och förbättring av kvalitetsutmaningar
Kunna agera i rollen som Software Test Lead, dvs att vara den ansvariga personen för alla testaktiviteter inom en release och vägleda kollegor från andra kompetensområden. 



Sista ansökningsdag: 1 mars 2020.
För frågor, kontakta rekryterande chef Johan Tschöp på tel. 18 61 200 69 eller e-post: [email protected]


Vänligen notera att denna roll kommer att ligga inom ramen för den föreslagna övergången av GE Biopharma till Danaher och kommer att övergå till Danaher när denna transaktion slutförs.


Kvalifikationer:
Minimum kandidatexamen inom mjukvaruutveckling eller jämförbar kompetensnivå
Erfarenhet inom testing av mjukvara
Kunskap om testautomatiseringsverktyg som tex UFT och SpecFlow samt testhanteringsverktyg t.ex. HP ALM
Flytande svenska och engelska, i tal och skrift



Önskvärda egenskaper:
Erfarenhet av bästa praxis för agil utveckling inklusive beteendedriven utveckling och testdriven utveckling, BDD och TDD
Självmotiverad personlighetmed förmågan att snabbt ta till sig, och praktiskt använda, ny teknik
Stark kommunikatör och problemlösningförmåga
Förmågan att samla ny information, förstå komplexa ämnen och sätta ihop de två
Gilla avancerade testfall och bidra till lösningen av buggar som hittats
Brinnande intresse för att förbättra processer, verktyg, miljöer
Intresse för både mjuk -och hårdvaruapplikationer med erfarenhet från kontrollmjukvarutestning, från enhet upp till systemtest
Erfarenhet från att testa applikationer för webb, moln och mobila enheter Visa mindre

Research Engineer

We are looking for a Research Engineer to our team Format & Functionality in the Resins department, Bioprocess R&D. You will belong to a team of 14 highly skilled engineers and scientists responsible for providing expertise in column packing and protein purification using chromatography in lab to process scale. The section is involved in research projects, new product development, product support and customer trainings. Essential Responsibilities: Develo... Visa mer
We are looking for a Research Engineer to our team Format & Functionality in the Resins department, Bioprocess R&D. You will belong to a team of 14 highly skilled engineers and scientists responsible for providing expertise in column packing and protein purification using chromatography in lab to process scale. The section is involved in research projects, new product development, product support and customer trainings.


Essential Responsibilities:
Developing packing methods for small scale chromatography columns used for purification of proteins that will support both new product introductions, market support and sales support
Perform laboratory investigations - on your own or as a team - through planning, execution and analysis of results
Take part in defining customer needs and verifying them
Present, orally and in writing, results and conclusions from studies performed

Please apply no later than 1 March 2020.
For questions, please contact hiring manager Camilla Larsson: [email protected]


Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


Qualifications/Requirements:
Master’s degree in Chemistry, Biotechnology, Biochemical/ Biomedical Engineering, Chemical engineering or related Life Sciences field or equivalent knowledge or experience
Structured and organized team player with good interpersonal skills with attention to details
Flexible and good track record to deliver according to deadlines
English and Swedish as working languages with good communication skills (both written and spoken)



Desired Characteristics:
Ability to simultaneously manage projects and other responsibilities and adjust quickly to changing priorities Visa mindre

Biopharma Sourcing - PMO Leader

Role Summary: The Sourcing Project Management Office (PMO) Leader will develop, implement and lead the supplier strategy and project execution for New Product Introductions (NPIs) across all franchises (P&Ls;), and for develop standard work and op mechs across the overall Sourcing project funnel for a new stand-alone Biopharma (BP) operating company. Lead a team of Product Sourcing Leaders accountable to meet the sourcing requirements across NPIs on-time, ... Visa mer
Role Summary:
The Sourcing Project Management Office (PMO) Leader will develop, implement and lead the supplier strategy and project execution for New Product Introductions (NPIs) across all franchises (P&Ls;), and for develop standard work and op mechs across the overall Sourcing project funnel for a new stand-alone Biopharma (BP) operating company. Lead a team of Product Sourcing Leaders accountable to meet the sourcing requirements across NPIs on-time, on-budget and with quality, integrity and compliance.


Essential Responsibilities:


• Develop a professional Project Management Organization within BP Sourcing
• Coach / educate / develop / attract project managers within Sourcing PMO Organization and identify and deploy appropriate PMO training(s) for the broader Sourcing organization
• Develop relevant dashboards to be used across the organization to share / escalate status on ongoing / future projects and ensure execution to project timelines and desired outcomes
• Co-animate Sourcing project streams across purchase families (commodities) to ensure alignment with x-functional team(s) on resources / execution / impact for VCP and SoS (security of supply) projects
• Educate / coach on PRD process / deliverables across the Direct Sourcing team
• Support PMO Sourcing leaders in projects execution – deliverables, escalations, counter-measures
• Define / drive standard work, standard sourcing deliverables and core KPIs for project execution across the business
• Develop appropriate dashboard for NPI Sourcing Healthcheck
• Be single point of contact (SPOC) for Engineering PMO leader, partnering to improve overall process flow, execution and impact across the project portfolio
• Drive regular alignment on project execution & NPI Healthcheck with leadership team


Specific to PMO Sourcing responsibilities:
• Maintain visibility on NPIs execution (contemporary NPI dashboard)
• Enforce early Sourcing engagement in NPIs on supplier selection and development in partnership with the Supplier Quality organization
• Ensure NPIs compliance with renewed NPI checklist
• Act as Sourcing reviewer on Project Milestones (if not owning project)
• Ensure Supply Chain and Item Risk Assessment guidance is deployed in NPI and transfer projects
• Act as project manager on assigned critical NPIs or critical VCP projects, leveraging Project Transfer Leaders in APAC, EMEA and USCAN.
• Handle Change Control process & Trackwise updates (by P&L)
• Coordinate required actions with wider sourcing team
• PMO Leader approves NPI Milestones
• Educate wider Sourcing team on NPI status / priorities




* The sale of the GE Healthcare Life Sciences Biopharma business to Danaher is subject to customary closing conditions, including regulatory reviews and appropriate consultation processes, and is expected to close as early as the first quarter of 2020.


Qualifications/Requirements:
1. Bachelor’s Degree in Engineering, Procurement, Supply Chain Management, or Finance
2. Minimum of 10 years experience in Sourcing, Operations, Supply Chain and/or Commercial background
3. Excellent business / financial acumen, proficient in leading and setting direction for teams, including demonstrated ability to motivate, influence and drive change at all levels of the organization
4. Excellent growth leadership skills demonstrating clear global perspective and understand factors impacting BP businesses and our suppliers
5. Willing to travel domestically and internationally up to 25% of time
6. Influence / communication - establishes good relationships; drives change across functional & global boundaries


Desired Characteristics:
1. Master in Business Administration
2. 15 years solid sourcing, supply chain or commercial experience including 10 years in a leadership capacity.
3. Extensive global experience leading cross-functional or geographically dispersed teams
4. Proven Executive Leadership skills in driving Global change across an organization, including strong Change Acceleration Process skills.
5. Demonstrated ability to lead courageously, maintaining a strong position amidst opposition to resolve important issues, and ability to navigate through a large complex business.
6. Project Management experience Visa mindre

Custom Parts Specialist within Life Sciences

The Life Sciences Service(LS) Custom Parts Specialist is responsible for driving world-class fulfilment of service spare parts transactions to enable high levels of customer (internal + external) satisfaction. Through strong collaboration with global supply chain, manufacturing sites, OEM/Suppliers, Global Services and Genpact. Essential Responsibilities: In the custom parts team (CPT) we supply our customers through the service organization with non-reg... Visa mer
The Life Sciences Service(LS) Custom Parts Specialist is responsible for driving world-class fulfilment of service spare parts transactions to enable high levels of customer (internal + external) satisfaction. Through strong collaboration with global supply chain, manufacturing sites, OEM/Suppliers, Global Services and Genpact.


Essential Responsibilities:
In the custom parts team (CPT) we supply our customers through the service organization with non-regular spare parts. The CPT member overlook and handle the whole chain from request to final delivery.
Main tasks include:
Interact with suppliers and our experts for fast response to the service organization on customized spare parts
Customer focus from start to the end through the whole chain
Ensure regular communication updates around custom parts status to stakeholders/customers
Contribute to the development and improvement of the quoting process
Responsible for creating the format for all packaging material used for custom spare part deliveries



Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


Qualifications/Requirements:
Engineering degree from high school/engineering college or corresponding degree or equivalent knowledge or experience
Strong work experience
Proven project management or direct or indirect people leadership experience
Self-motivated, self-starter with the ability to work independently and learn quickly
Understand that the customers determine our success
Knowledge on engineering design principles, architectures and advancements in engineering concepts and technologies
Effective communication skills and boundless behavior—ability to present ideas and cases clearly and concisely
Experience of working in project teams meeting deadlines and deliverables
Fluent speaking and writing in English language
Applicable Work-Permit



Desired Characteristics:
Technical degree such as B Sc in Engineering or similar or equivalent knowledge or experience
Experience working in a Service or Systems Engineering team
Experience of PDMsystems (Magic)
Experience of defining requirement specifications
Proven ability to work cross functionally
Demonstrated supplier and manufacturing interface skills
Excellent communication, influencing skills and ability to gain buy-in for initiatives
Proven LEAN skills
Demonstrated problem-solving and leadership skills Visa mindre

Global Product Manager Filtration HW

Role Summary: Summary: We are searching for a commercially experienced Global Product Manager to join the BioProcess standard Downstream Hardware team. Your main responsibility will be to manage the Filtration hardware portfolio, a growing part of the BioProcess Hardware business. You will develop strategies and tactical execution plans for the products in order to maximize sales and profitability over the products' life cycle. Essential Responsibilities... Visa mer
Role Summary:
Summary: We are searching for a commercially experienced Global Product Manager to join the BioProcess standard Downstream Hardware team. Your main responsibility will be to manage the Filtration hardware portfolio, a growing part of the BioProcess Hardware business. You will develop strategies and tactical execution plans for the products in order to maximize sales and profitability over the products' life cycle.


Essential Responsibilities:


Key aspects of the role include:


Represent customer interests for your product(s) inside GE. Ensuring customer focus by building rapport with customers as required and ensuring the "voice of the customer" is reflected in work processes
Develop a product life cycle strategy and recommend investment and NPI development. Manage all aspects of the product(s)' life cycle including pricing, marketing and supply chain related recommendations
Drive the overall product development process for NPIs. Create business cases and adjust/monitor before and during product development and launch. Prepare and implement product launch plans, coordinating with commercial stakeholders to define go-to-market strategy
Define and recommend value engineering of products redesign to extend life cycle. Provide input and prioritization to R&D and Supply chain on requirements for support, product care and research & development projects, including customizations
In close collaboration with other product managers, R&D and Service make sure that the product strategies are in-line with business priorities in adjacent areas such as filtration consumables and automation
Ensure targets for production cost, inventory levels and quality are met. Provide leadership to Quality, Sourcing and Supply Chain functions to ensure the portfolio retains and improves upon its position in these areas
Provide sales and profitability forecasts to internal stakeholders
Support commercial organisation with marketing material and sales tools
Coordinating the needs across a multi-functional organization, including marketing, sales, operations, engineering, and services teams, while ensuring compliance with quality systems and regulatory requirements
Close collaboration with marketing to translate practice needs, market analysis, competitive analysis, and regulatory environment factors into actionable strategies and tactics for the product
Own the pricing strategy and its implementation for your product(s)
Ensure product readiness for sale and use. Manage such things as product registration, labelling, legal and safety requirements, storage conditions, logistics, technical content of databases, and after sales support together w Service



Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


For more information please contact Kristina Uhlen +46 706120838 [email protected]
Last day to apply is March 22nd.


Qualifications/Requirements:


Bachelor’s Degree in Engineering/Life Sciences/Biotechnology
Proven experience in a Life Sciences based business, including experience in marketing, sales, or product management
Major experience in Process science or related field including workflow experience with similar products
Experience of customer/market focused activities
Strong business and technical acumen
Good interpersonal and communication skills, plus experience of using these skills to participate in and influence cross-functional teams
Ability to work effectively in a matrix environment
For work in Sweden EU work permit is required



Desired Characteristics:


Sales experience
Marketing Diploma or equivalent
Awareness of GEHC product portfolio that serves this market
Good understanding of the filtration technologies and applications
Good understanding of the biopharmaceutical manufacturing environment and the needs of the customers in this market
Proven ability and expertise in working to combine hardware and automation with a customer focused mindset
Team oriented
Ability to motivate and work well with diverse, cross-functional teams
Operates in a goal-oriented way with proven personal drive and delivery performance Visa mindre

Laboratoriespecialist- vikariat

Vi söker en till medarbetare till våran Quality Control verksamhet i Uppsala. Gillar du labbarbete och är kvalitetsmedveten så kan detta vara rätt roll för dig! Avdelningen Quality Control arbetar med att analysera och kvalitetskontrollera vår produktion inom Chemical Production Uppsala (CPU). Rollen är en visstidsanställning. Huvudsakliga arbetsuppgifter: I rollen som laboratoriespecialist arbetar du främst med att kvalitetskontrollera produkter enlig... Visa mer
Vi söker en till medarbetare till våran Quality Control verksamhet i Uppsala. Gillar du labbarbete och är kvalitetsmedveten så kan detta vara rätt roll för dig!


Avdelningen Quality Control arbetar med att analysera och kvalitetskontrollera vår produktion inom Chemical Production Uppsala (CPU).
Rollen är en visstidsanställning.


Huvudsakliga arbetsuppgifter:
I rollen som laboratoriespecialist arbetar du främst med att kvalitetskontrollera produkter enligt gällande instruktioner och rutiner samt bedöma om analysstatus
Avrapportera, kontrollgranska och utföra analysacceptans på produkter och uppdragsanalyser
Starta och driva undersökningar vid avvikande analysresultat och andra avvikelser
Utföra kontroller, kalibreringar och underhåll av analysinstrument
Uppdatera och godkänna arbetsinstruktioner (kontrollmetoder, standardmetoder och kalibreringsmetoder)
Analysera och avrapportera analysresultat inom överenskomna ledtider.
I samband med analysacceptans följa analysmetoders prestanda genom trendning.
Arbeta för att hålla metoder och instrument/utrustningar funktionsdugliga och tillförlitliga.
Säkerställa att instrument och utrustningar är kvalificerade och har tillräcklig nivå på kontroll, kalibrering och underhåll.
Öppna och utreda avvikande analysresultat.



Kvalifikationer:
Lämplig bakgrund är högskoleingenjör/ gymnasieingenjör inom Kemi/Analytisk Kemi/ Biokemi eller liknande.


Vi söker någon som är:
noggrann och strukturerad
flexibel
bra på att samarbeta
positiv, uppmuntrar och inspirerar andra
stresstålig och kan utföra flera olika arbetsuppgifter parallellt
gillar att arbeta i förändring och driva förändringsarbete



Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


Önskvärda egenskaper:
Tidigare erfarenhet av laborativt kvalitetsarbete inom QC-verksamhet, gärna inom kromatografi
Datorvana MS Office
Protein-kemi Visa mindre

Technical Product Owner

Role Summary: The product owner will be responsible for creating and prioritizing the application technical road map, this application helps scientists reduce the time to insights by aggregating, integrating and sharing laboratory data, and structure it for future needs and innovation capture. Essential Responsibilities: Works directly with Product Management to understand the strategic product road map Builds relationships with both internal and exter... Visa mer
Role Summary:
The product owner will be responsible for creating and prioritizing the application technical road map, this application helps scientists reduce the time to insights by aggregating, integrating and sharing laboratory data, and structure it for future needs and innovation capture.


Essential Responsibilities:


Works directly with Product Management to understand the strategic product road map
Builds relationships with both internal and external customers to research user needs and gather requirements
Collaborates with multiple teams (UX, Product Management, Functional, etc.) to execute and deliver the product road map
Creates high-level stories and features that will serve as the foundations for Technical Product Managers and Scrum Teams to build on
Works directly with Scrum Masters to define, prioritize and maintain the product backlog
Communicates effectively across the organization, including leadership, to ensure the product road map is aligned with business objectives.
Support product management and quality teams in ensuring product compliance, including but not limited to GDPR, HIPAA, IP and ISO.
Support product management and quality teams in ensuring operational compliance, including but not limited to disaster recovery, backup procedures and business continuity plans



Qualifications/Requirements:


University degree or extensive experience in Biochemistry/Biotechnology or equivalent Life Science discipline, preferably with experience in process sciences or related fields
Extensive experience in an informational technology field, preferably in software development and implementation
2-4 years’ experience working in digital product management, preferably focused on products within the Life Sciences industry
Experience working within Agile Product teams, specifically scrum
Ability to work effectively in a collaborative, matrixed, Global and customer focused environment
Ability to work effectively across functions to deliver results and execute multiple commitments within the Global Environment.



Desired Characteristics:


Knowledge of software development and agile methodologies and structure (Theme/Epic/Feature/User stories). Certifications are a plus
Strong project management skills with the ability to communicate key metrics to all levels of stakeholders
Ability to be a single point of contact and communicate across multiple teams and organizations
Ability to break down problems, document problem statements and drives issue resolution
Ability to mentor, influence and guide team members and stakeholders
Strong oral, written and interpersonal communication skills
Experience with Amazon Web Services and relevant programming languages are a benefit, but not required Visa mindre

Sourcing specialist

Som Sourcing Specialist på GE Healthcare ansvarar du för att genomföra inköpsstrategier för en leverantörsportfölj. Leverantörerna finns både i Sverige och internationellt och kan vara allt från mindre företag till stora koncerner. Arbetet innebär många externa och interna kontakter med nära samarbete med våra produktionsenheter i Umeå och Uppsala. Du jobbar tillsammans med en erfaren Sourcing Leader och bidrar till utvecklingen av långsiktiga strategier. ... Visa mer
Som Sourcing Specialist på GE Healthcare ansvarar du för att genomföra inköpsstrategier för en leverantörsportfölj. Leverantörerna finns både i Sverige och internationellt och kan vara allt från mindre företag till stora koncerner. Arbetet innebär många externa och interna kontakter med nära samarbete med våra produktionsenheter i Umeå och Uppsala. Du jobbar tillsammans med en erfaren Sourcing Leader och bidrar till utvecklingen av långsiktiga strategier.


Huvudsakliga arbetsuppgifter:
Genomföra inköpsstrategier för en portfölj av leverantörer, med fullt ansvar för att möta mål för kostnadsbesparingar genom exempelvis förhandling eller förändringar av försörjningskedjan.
Förhandla avtal med leverantörer.
Bevaka leveransprecision och kvalitetsutfall samt utveckla och genomföra strategier som möter interna kunders behov av förbättringar.
Bidra till utvecklingen av nya produkter genom att stödja med offerthantering och förhandling av priser i projekt.
Underhålla leverantörsdata i affärssystem, inklusive uppsättning av nya artiklar och prisjusteringar.



Kvalifikationer:
Högskoleingenjör eller civilingenjör inom mekanik, industriell ekonomi eller liknande, alternativt motsvarande erfarenhet.
Ett par års erfarenhet av inköpsarbete, produktionsberedning, produktutveckling eller liknande
Erfarenhet av Microsoft Office
Flytande engelska i tal och skrift
Arbetstillstånd för Sverige



Önskvärda egenskaper:
Vi ser helst att du har en bred teknisk bakgrund med specifika kunskaper i maskinbearbetning av metall och plast.
Du är duktig på att kommunicera, presentera och bygga relationer med leverantörer såväl som med interna intressenter.
Din tidigare erfarenhet visar att du är pålitlig och håller vad du lovar.
Jobbet innebär en hel del analys av data och underhåll av information i affärssystem, därför är avancerade kunskaper i Excel samt erfarenhet av Oracle meriterande. Visa mindre

Laboratoriespecialist

Vi söker en till medarbetare till våran Quality Control verksamhet i Uppsala. Gillar du labbarbete och är kvalitetsmedveten så kan detta vara rätt roll för dig! Avdelningen Quality Control arbetar med att analysera och kvalitetskontrollera vår produktion inom Chemical Production Uppsala (CPU). Huvudsakliga arbetsuppgifter: Rollen som laboratoriespecialist arbetar du främst med att kvalitetskontrollera produkter enligt gällande instruktioner och rutiner... Visa mer
Vi söker en till medarbetare till våran Quality Control verksamhet i Uppsala. Gillar du labbarbete och är kvalitetsmedveten så kan detta vara rätt roll för dig!


Avdelningen Quality Control arbetar med att analysera och kvalitetskontrollera vår produktion inom Chemical Production Uppsala (CPU).


Huvudsakliga arbetsuppgifter:
Rollen som laboratoriespecialist arbetar du främst med att kvalitetskontrollera produkter enligt gällande instruktioner och rutiner samt bedöma om analysstatus.
Arbetsuppgifter inkluderar:
Avrapportera, kontrollgranska och utföra analysacceptans på produkter och uppdragsanalyser.
Starta och driva undersökningar vid avvikande analysresultat och andra avvikelser.
Utföra kontroller, kalibreringar och underhåll av analysinstrument.
Uppdatera och godkänna arbetsinstruktioner (kontrollmetoder, standardmetoder och kalibreringsmetoder).
Analysera och avrapportera analysresultat inom överenskomna ledtider.
I samband med analysacceptans följa analysmetoders prestanda genom trendning.
Arbeta för att hålla metoder och instrument/utrustningar funktionsdugliga och tillförlitliga.
Säkerställa att instrument och utrustningar är kvalificerade och har tillräcklig nivå på kontroll, kalibrering och underhåll.
Öppna och utreda avvikande analysresultat.

Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


Kvalifikationer:
Lämplig bakgrund är högskoleingenjör/ gymnasieingenjör inom Kemi/Analytisk Kemi/ Biokemi eller liknande.



Vi söker någon som är:
noggrann och strukturerad
flexibel
bra på att samarbeta
positiv, uppmuntrar och inspirerar andra
stresstålig och kan utföra flera olika arbetsuppgifter parallellt
gillar att arbeta i förändring och driva förändringsarbete



Desired Characteristics:
Tidigare erfarenhet av laborativt kvalitetsarbete inom QC-verksamhet, gärna inom kromatografi
Datorvana MS Office
Protein-kem Visa mindre

Fast Trak Downstream Research Engineer

We are looking for an 18 month temporary position as a Downstream Research engineer for Fast Trak, a global group that oversees the biopharma industry. The position is in a highly dynamic group that supports customers from industry/academia with process development services for various biomolecules as well as training courses. Given its diverse functions, Fast Trak nurtures a highly collaborative and exciting environment and provides many opportunities ... Visa mer
We are looking for an 18 month temporary position as a Downstream Research engineer for Fast Trak, a global group that oversees the biopharma industry.


The position is in a highly dynamic group that supports customers from industry/academia with process development services for various biomolecules as well as training courses. Given its diverse functions, Fast Trak nurtures a highly collaborative and exciting environment and provides many opportunities for individual career development.


Essential Responsibilities:
Working directly with customers in a strong collaborative environment
To host/train Customers (internal/external)
Support with lab management
To maintain accurate and complete records of all work, and report results in oral and written manner
Assisting in delivering scientific application work on downstream process development and process transfer projects (e.g. Monoclonal Antibodies (MAb's), vaccines, recombinant proteins). Work can include performing experiments using ÄKTA platform as well as performing analytical experiments (HPLC, SDS-PAGE etc)
Assist in delivering training courses for customers, theoretical as well as practical, in the field of biomanufacturing
Developing and maintaining relationships with the regional commercial and marketing teams, as well as the global Fast Trak and R&D organizations
Occasional international travel may occur

For more information regarding this position please contact hiring manager Kristina Nilsson-Välimaa ([email protected])
Last day to apply is February 1st March.


Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


Qualifications/requirements:
Master’s degree in chemistry, Physics, Biotechnology, Biochemical/ Biomedical Engineering, Chemical engineering or related Life Sciences field or equivalent knowledge or experience
Experience in operating ÄKTA systems and UNICORN software
Basic knowledge of chromatography
Able to simultaneously manage projects and other responsibilities and adjust quickly to changing priorities
Strong presentation and communication skills
Structured and organized team player with good interpersonal skills
Interest to work in a collaborative, matrixed, and customer focused environment
Demonstrated advanced English skills both written and spoken



Desired Characteristics:
Prior teaching and/or presenting scientific material experience would be highly desirable Visa mindre

Scientist/Senior Scientist

We are looking for a Scientist/Senior Scientist to join the Bioprocess Application section within the R&D Downstream Resins department. The section is based in Uppsala and consists of about 10 biochemists and application specialists within the area of purification of viral vectors, recombinant proteins, plasma and monoclonal antibodies. The position is focused on the development of purification- and analysis methods for viral vectors such as AAV and lenti... Visa mer
We are looking for a Scientist/Senior Scientist to join the Bioprocess Application section within the R&D Downstream Resins department.
The section is based in Uppsala and consists of about 10 biochemists and application specialists within the area of purification of viral vectors, recombinant proteins, plasma and monoclonal antibodies. The position is focused on the development of purification- and analysis methods for viral vectors such as AAV and lentiviruses.


Essential Responsibilities:
The position includes active participation in research and development projects where you will contribute with expertise within the field of viral vectors, in particular AAVs.
You will be working in a team that is focused on developing and establishing efficient purification procedures for viral vectors using existing products or products under development.
The position involves developing and establishing analytical methods typically used in the manufacturing and characterization of viral vectors, such as qPCR and, ELISA.
In addition you will be participating in the evaluation of newly developed purification resins for viral vectors.
You are also expected to identify, develop and maintain external networks within the field as well as act as activity leader of section activities within a project.



Please apply no later than 8 March 2020. For questions, please contact hiring manager Tobias Cornvik: tel. +46 73 063 57 52 or [email protected]


Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


Qualifications/Requirements:
Ph.D. degree in virology, analytical sciences, or related field
Technical knowledge and practical experience of the preparation of viral vectors or viruses is highly desirable
Proven ability of planning, executing and evaluating analytical & preparative experiments
Considerable knowledge and experience of Biotechnology/Biochemistry, experience from viral vectors or virology
Familiarity with analytical methods typically used in the manufacturing and characterization of viral vectors, e.g. ELISA, qPCR or ddPCR
Strong interest and skills in practical laboratory work
Scientific leadership skills
Excellent communication skills (both written and spoken), including presentation skills.Goal-oriented team worker
English as a working language





Desired Characteristics:
Experience of working with purification / downstream process of viral vectors, preferably AAV or lentivirus
Knowledge and experience with AAV biology
Fluent in Swedish Visa mindre

Fast Trak Scientist

We are looking for a 18 months temporary position for a Downstream Scientist for Fast Trak, a global group that oversees the biopharma industry. The position is in a highly dynamic group that supports customers from industry/academia with process development services for various biomolecules as well as training courses. Given its diverse functions, Fast Trak nurtures a highly collaborative and exciting environment and provides many opportunities for indi... Visa mer
We are looking for a 18 months temporary position for a Downstream Scientist for Fast Trak, a global group that oversees the biopharma industry.


The position is in a highly dynamic group that supports customers from industry/academia with process development services for various biomolecules as well as training courses. Given its diverse functions, Fast Trak nurtures a highly collaborative and exciting environment and provides many opportunities for individual career development


Essential Responsibilities:
Working directly with customers in a strong collaborative environment
Conducting independent scientific application work on key projects such as (Monoclonal Antibodies (MAb's), vaccines, recombinant proteins, plasma fractionation)
Developing and delivering training courses for customers, theoretical as well as practical, in the field of biomanufacturing
Maintain accurate and complete records of all work, and report to customers and management in oral and written manner
Ensuring integrity and compliance with quality systems, and EHS requirement
Developing and maintaining relationships with the regional commercial teams, as well as the global Fast Trak and R&D organizations
Identifying improvement opportunities in GE customer's bio-manufacturing processes
Occasional international travel may occur



Please contact Kristina Nilsson Välimaa 076-4950123 for more information about the position


Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.
Qualifications/Requirements:
PhD or Masters degree in Chemistry, Physics, Biomedical Engineering, Chemical engineering or related Life Sciences field or equivalent knowledge or experience
Significant experience in downstream process development, scale-up, tech transfer, and/or manufacturing
To be successful in this role, you enjoy working in a high pace environment with frequent changes
Demonstrated strong presentation and communication skills
Structured and organized team player with good interpersonal skills
Demonstrated advanced English skills both written and spoken



Desired Characteristics:
Industrial experience in Downstream processing of biomolecules (filtration, downstream, technology transfer, validation, process development, biomanufacturing, continuous processing)
Demonstrated ability to work in a collaborative, matrixed, and customer focused environment
Prior teaching and/or presenting scientific material experience would be highly desirable Visa mindre

IT Infrastructure Business Analyst

Role Summary/Purpose This position will work closely with functional process owners in Biopharma R&D to analyze strategic and tactical requirements and plan for delivery of operational technology (OT) and IT solutions. You will build strong business stakeholder relationships as well as maintaining a strong network in the IT community. Essential Responsibilities •        Build and maintain relationship with business partners in defined process area •   ... Visa mer
Role Summary/Purpose
This position will work closely with functional process owners in Biopharma R&D to analyze strategic and tactical requirements and plan for delivery of operational technology (OT) and IT solutions.
You will build strong business stakeholder relationships as well as maintaining a strong network in the IT community.


Essential Responsibilities


•        Build and maintain relationship with business partners in defined process area
•        Effectively uncover, align and manage stakeholders needs and expectations
•        Lead business process workshops to understand business needs and build robust business cases
•        Manage strategic and tactical IT planning for defined process area
•        Translate high-level business requirements into detailed specifications and cost estimates
•        Work closely with the teams for delivery and operation to support quality in delivery of solutions and continuous excellence of support of solutions
•        Lead vendor evaluation analysis
•        Lead small project initiatives
•        Provide hands on server management like security patching or other vulnerability remediation activities


Required qualifications


•        Some years of experience of IT Infrastructure work
•        Experience with Linux and/or Windows server environments and storage solutions
•        Experience as a server administrator, file share administrator
•        Some experience in network topology and concepts
•        Awareness of active Directory, domain policies and Citrix solutions
•        Experience working in a business stakeholder/customer environment translating requirements into infrastructure specifications
•        Ability to influence and negotiate with clients and suppliers
•        Proficient at operating within a globally distributed team
•        Strong analytical skills
•        Strong collaboration skills
•        Excellent written and oral communication skills




Desired Characteristics


•        Bachelor's Degree
•        Experience in the healthcare industry
•        Appetite for new technology, willingness to be very hands-on in technology area
•        Lean experience
•        Strong can-do attitude Visa mindre

Ecosystems Leader

Role Summary: You will be responsible for the delivery data related systems for Biopharma. This is a new area of responsibility for Biopharma IT, the systems have previously been provided and supported by GE Healthcare and many of them will continue to be supported for a transitional period under a Services Agreement (TSA). Essential Responsibilities: Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to ... Visa mer
Role Summary:


You will be responsible for the delivery data related systems for Biopharma. This is a new area of responsibility for Biopharma IT, the systems have previously been provided and supported by GE Healthcare and many of them will continue to be supported for a transitional period under a Services Agreement (TSA).


Essential Responsibilities:
Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction. 


This role will be responsible for:
Standing up ecosystems for Payroll and T&L accounting
Will need to work closely with the Sourcing team and enable the accounting and reconciliation activities for all Source to Pay activities
Work closely with the Intercompany team to implement an automated solution for the accounting activity
Ensure stability on all Treasury related activity (e.g. automated payments and cash reconciliation)
Work closely with the Supply Chain and Operations’ teams ensuring that the accounting activities are captured efficiently within the ERP



The immediate focus will be on building out the capabilities and delivering to the business, enabling the TSA exit on all applications that are connected to these capabilities. These strategic apps will then need to be aligned for future growth of the organisation ensuring scalability allowing for future expansion. 


Applications from job seekers who require sponsorship to work in the UK are welcome and will be considered alongside all other applications. However, non-EU/EEA candidates may not be appointed to a post if a suitably qualified, experienced and skilled EU/EEA candidate is available to take up the post, as the employing body is unlikely, in these circumstances, to satisfy the Resident Labour Market Test. For further information please visit the UK Border Agency website .


Qualifications/Requirements:
Bachelor's Degree in Computer Science or “STEM” Majors (Science, Technology,
Engineering and Math) or equivalent knowledge or work experience 
Proved professional experience



Desired Characteristics:


Technical Expertise:
Hands on experience of delivery of Finance IT systems (e.g. Concur, Kyriba, CoStar, etc.) including release management, operations and maintenance
Familiarity with agile and other delivery methodologies
Ability to support teams to identify new approaches to complex design problems
Awareness of applications architecture and an appreciation of wider Finance IT ecosystems
Business Acumen: Ability to evaluate technology to deliver to the business vision, ensuring that technical innovation matches outcomes and value proposition
Ability to influence non-technical aspects of technology change (e.g. business processes and operational architectures)
Problem solver; demonstrated ability to plan and execute highly visible, cross business initiatives
Proven experience in leading IT initiatives and to provide thought leadership to a team
Passionate about technology with the pragmatism necessary to solve customer problems and deliver value
Creates a culture of customer focus and high performance to drive innovation aligned to business outcomes 



Personal Attributes:
A strong sense of ownership, urgency, and drive
Ability to work independently and collaboratively
Proactively engages with cross-functional teams to resolve issues and design solutions
Exhibits creativity and new ways of thinking when contributing to organizational and individual objectives
Strong verbal presentation and written communication skills
Strong influencing and collaboration skills
Uses critical thinking skills and disciplined approaches to help resolve issues and define solutions Visa mindre

Product Manager Microcarriers

Role Summary: This role provides multi-functional leadership and strategic direction for GE’s Microcarrier portfolio including the Cytodex and Cytodex Gamma brands. You will own the portfolio from product roadmap to organization readiness and product/service delivery. Essential Responsibilities: Working collaboratively with commercial teams, supply chain, R&D and other functions to drive revenue and profitability of the business. Additionally, this... Visa mer
Role Summary:


This role provides multi-functional leadership and strategic direction for GE’s Microcarrier portfolio including the Cytodex and Cytodex Gamma brands. You will own the portfolio from product roadmap to organization readiness and product/service delivery.


Essential Responsibilities:


Working collaboratively with commercial teams, supply chain, R&D and other functions to drive revenue and profitability of the business.


Additionally, this position will focus on evaluating our existing portfolio and developing organic and inorganic strategies to expand and drive incremental growth. This will require leadership through influence and participation in key business decision making forums such as R&D Portfolio, Product Care, Product Quality, and Sales & Operations planning.




Management of the Microcarrier portfolio over its life cycle within a product portfolio of a business area in a manner that maximizes the overall return/profit to the company, within the context of company, business area and marketing plans. Ensures compliance with quality systems, regulatory requirements, and commercial change process.
Manages all aspects of the product(s) life cycle starting with the detailed planning phase until the product is terminated. Define Product Models, Offerings and Structures.
Develop strong cross functional relationships with Supply Chain, R&D, Quality, Sourcing and other key functions to successfully drive both short-term and long-term projects to strengthen product offerings.
Partner with marketing to create compelling customer facing material, and commercial sales tools.
Maintain customer focus on value of Microcarrier products. Represent voice of customer internally to advocate for customer needs.
Establish and maintain strong working relationships with commercial team members including account managers and modality experts.
Become a product/business expert in Microcarriers. Function as the point of contact for questions and problem solving for internal business partners and external customers.
Support the establishment/refinement of product management processes, including annual road-mapping and pricing review.
Identify market trends and opportunities in the Bioprocess Microcarrier landscape.



Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


For more information about the position please contact Jon Van Pelt [email protected] or +1 508 683 3745


Last day to apply is February 28th


Qualifications/Requirements:


Bachelor’s Degree in Marketing, Engineering, Science, Business Administration or related field or equivalent knowledge or experience.
Extensive experience in product marketing, product development, or related field.
Product Management/Marketing expertise, including: market trends/analysis, NPI process, product roadmap development, product life-cycle management.
Excellent oral and written communications skills in English. Swedish also an advantage.
Strong analytical and process skills.
Strong project management skills.
Ability to work effectively within a matrix environment



EU Work permit Visa mindre

BioPharma Indirect Sourcing Leader

Role Summary: The Indirect Sourcing Leader will be the key point of contact for sourcing activities in the Logistics Category. The role will report directly to the Biopharma Sourcing Manager for Logistics and be a key member of the Indirect sourcing team to ensure global strategies are developed and deployed in partnership with the business stakeholders. Essential Responsibilities: In this role, the Indirect Sourcing Leader will take the lead for sourcing ... Visa mer
Role Summary:
The Indirect Sourcing Leader will be the key point of contact for sourcing activities in the Logistics Category. The role will report directly to the Biopharma Sourcing Manager for Logistics and be a key member of the Indirect sourcing team to ensure global strategies are developed and deployed in partnership with the business stakeholders.
Essential Responsibilities:
In this role, the Indirect Sourcing Leader will take the lead for sourcing activities in the regions, to ensure the business have the right partners both from a cost, quality and business growth perspective.


NOTE: GE employees may be considered for this role. Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction. For at least two (2) years post the proposed close sale date* Biopharma employees will not be able to transfer into any role in other parts of GEHC or in another GE business.


* The sale of the GE Healthcare Life Sciences Biopharma business to Danaher is subject to customary closing conditions, including regulatory reviews and appropriate consultation processes, and is expected to close as early as the first quarter of 2020.


• Be a key partner to the business on matters related to sourcing activites in the Logistics category, covering freight, warehousing, packaging and brokerage.
• Provide sourcing leadership and support to stakeholders at all levels of the organization in the effort of building a strong partnership with key suppliers.
• Be the subject matter expert on the supply chain marked conditions, latest trends, innovation and cost control. Warehousing experience highly desired.
• Lead and drive the sourcing process from RFP, RFQ and contract development.
• Lead regular sourcing reviews with internal stakeholders and external suppliers.
• Faclitate cross-functional workouts and efforts as related to sourcing processes, procedures and related cost improvements.
• Support internal stakeholders on business growth and expansion plans.
• Build strategic sourcing road maps based on business growth and customers needs.
• Drive Simplification projects on sourcing processes and tools.
• Conduct training on sourcing processes and serve as key point of contact on sourcing inquiries.
• Drive sourcing process compliance; Provide input to, and support of procedures and guidelines as necessary.


Qualifications/Requirements:
• MCIPS or equivalent Professional Procurement qualification, or BA or BS degree or other advanced degree in Supply Chain, Purchasing, Economics or equivalent.
• At least 5 years of experience in Sourcing, Project Management, Finance, or Logistics Operations.
• Excellent interpersonal communications and negotiation skills with ability to influence at all levels of the organization.
• Strong analytical skills, BI development and database management skills.
• Strong communication (verbal, written & presentation); skilled in working collaboratively with remote personnel.
• Self starter who can work independently with key stakeholders at all levels of the organization.
• Strong Project management & process improvement skills.
• Applicable work permit


Desired Characteristics:
• Fluent English both verbal and written. 2nd language preferred.
• Green or Black Belt certified/ Lean experience.
• Excellent communication skills.
• Experience with Oracle, TMS, WMS, Qlick or other relevant BI and purchasing tools.
• Experience leading simplification projects.
• Experience in the logistics industry.
• Experience with divestitures. Visa mindre

Data Leader

Role Summary: You will be responsible for the delivery data related systems for Biopharma. This is a new area of responsibility for Biopharma IT, the systems have previously been provided and supported by GE Healthcare and many of them will continue to be supported for a transitional period under a Services Agreement (TSA). Essential Responsibilities: Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Da... Visa mer
Role Summary:
You will be responsible for the delivery data related systems for Biopharma. This is a new area of responsibility for Biopharma IT, the systems have previously been provided and supported by GE Healthcare and many of them will continue to be supported for a transitional period under a Services Agreement (TSA).


Essential Responsibilities:
Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


This role will oversee:
Master Data Management (MDM) and provision of MDM across all systems
Responsible for Data Consolidation in the new EPM environment and ensuring the new EPM environment is appropriately designed and fit for purpose
Work closely with the Financial reporting team to ensure we have optimised reporting capability
Work closely with the STAT / regulatory reporting team to ensure we have optimised reporting capability
Work closely with the Business Intelligence team and ensure we have the right toolset for all end user reporting needs



The immediate focus will be on building out the capabilities and delivering to the business, enabling the TSA exit on all applications that are connected to these capabilities. These strategic apps will then need to be aligned for future growth of the organisation ensuring scalability allowing for future expansion.


Qualifications/Requirements:
Bachelor's Degree in Computer Science or “STEM” Majors (Science, Technology,
Engineering and Math) or equivalent knowledge or work experience
Proven professional experience



Desired Characteristics:


Technical Expertise:
Hands on experience of delivery of Finance IT systems (e.g. Oracle DRM, Hyperion, Data Warehouse, BOXI, QLIK, etc.) including release management, operations and maintenance
Familiarity with agile and other delivery methodologies
Understanding of Finance Data Analytics and dashboard systems
Ability to support teams to identify new approaches to complex design problems
Well developed analytical skills
Awareness of applications architecture and an appreciation of wider Finance IT ecosystems
Business Acumen: Ability to evaluate technology to deliver to the business vision, ensuring that technical innovation matches outcomes and value proposition
Ability to influence non-technical aspects of technology change (e.g. business processes and operational architectures)
Problem solver; demonstrated ability to plan and execute highly visible, cross business initiatives
Proven experience in leading IT initiatives and to provide thought leadership to a team
Passionate about technology with the pragmatism necessary to solve customer problems and deliver value
Creates a culture of customer focus and high performance to drive innovation aligned to business outcomes 



Personal Attributes:
A strong sense of ownership, urgency, and drive
Ability to work independently and collaboratively
Proactively engages with cross-functional teams to resolve issues and design solutions
Exhibits creativity and new ways of thinking when contributing to organizational and individual objectives
Strong verbal presentation and written communication skills
Strong influencing and collaboration skills
Uses critical thinking skills and disciplined approaches to help resolve issues and define solutions Visa mindre

European Patent Attorney

Role Summary: Reporting to a more senior GE Biopharma IP Counsel, this role will provide an opportunity to work with a cross-functional team on specific aspects of patent strategy across GE’s Biopharma business. The successful candidate will be responsible for drafting patent applications and prosecuting a global patent portfolio, including acting as the European representative before the European Patent Office for European applications. Essential Respon... Visa mer
Role Summary:
Reporting to a more senior GE Biopharma IP Counsel, this role will provide an opportunity to work with a cross-functional team on specific aspects of patent strategy across GE’s Biopharma business. The successful candidate will be responsible for drafting patent applications and prosecuting a global patent portfolio, including acting as the European representative before the European Patent Office for European applications.


Essential Responsibilities:
This role will also encompass:
general IP counseling
managing idea generation
opposition work
freedom-to-operate reviews
licensing and enforcement


All GE employees may be considered for this role. Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


Qualifications/Requirements:
European Patent Attorney.
Technical background in electrical, chemical or mechanical engineering, software, physics or equivalent.
Excellent written and oral communication skills.
Capable of devising innovative IP strategies


Desired Characteristics:
Knowledge of laws, regulations, practices and procedures relating to patent procurement in Europe, US and Asia.
Technical experience working in the life sciences or healthcare sector, advantageously: in bioprocessing; fluidic; and/or electromechanical control fields.
Experience acting as European representative before the European Patent Office.
Experience prioritizing competing demands to make real time decisions/recommendations in a fast-paced environment.
Demonstrated ability to quickly identify & prioritize issues, develop process-driven solutions, and effectively communicate with a wide range of people. Visa mindre

Mekanikingenjör

Arbete som Mekanikingenjör sker inom Kemisk Tillverkning i Uppsala, avdelning QC på sektion QC Material Supply. Sektionen består av 17 personer varav 2 personer arbetar på mekaniklabbet (där denna tjänst ingår). Sektionen har två huvudsakliga syften: att kvalitetskontrollera och fatta beslut om status för inköpt material (kemiska råvaror och komponenter) att ansvara för sajtens råvaruförråd som hanterar in- och utleveranser av inköpt material Huvudsakli... Visa mer
Arbete som Mekanikingenjör sker inom Kemisk Tillverkning i Uppsala, avdelning QC på sektion QC Material Supply. Sektionen består av 17 personer varav 2 personer arbetar på mekaniklabbet (där denna tjänst ingår). Sektionen har två huvudsakliga syften:
att kvalitetskontrollera och fatta beslut om status för inköpt material (kemiska råvaror och komponenter)
att ansvara för sajtens råvaruförråd som hanterar in- och utleveranser av inköpt material



Huvudsakliga arbetsuppgifter:
Som Mekanikingenjör arbetar du främst med ankomstkontroll av mekanikmaterial och fattar/verkställer status på dessa. I tjänsten ingår även att arbeta med avvikelsehantering, grundorsaksutredningar och ständiga förbättringar m a p kvalitet, förenkling och EHS. Som Mekanikingenjör fungerar du även som back up till sektionens Product Quality Engineer för inköpt mekanikmaterial. I rollen ingår även att fungera som resurs inom QC-avdelningen inom områden där den egna kompetensen är god.
Ankomstkontroll av inköpt mekanikmaterial, kontrollgranskning av kollegors mätresultat och fatta beslut/verkställa beslut om status
Självständigt driva arbete kring avvikelsehantering, genomföra grundorsaksanalyser och implementera åtgärder
Arbeta systematiskt med förbättringsarbete inom kvalitet, förenkling och EHS (arbetsmiljö)
Fungera som ersättare för sektionens Product Quality Engineer (PQE) för mekanikmaterial vid dennes frånvaro



Kvalifikationer:
Högskoleexamen eller motsvarande inom relevant teknikområde (mekanik, maskin) eller annan lämplig utbildning kombinerad med erfarenhet från bioteknisk eller läkemedelsindustri
Erfarenhet av kvalitetskontroll och beslutsfattande av status m a p komponenter inom bioteknisk/läkemedelsindustri
Erfarenhet av mekanisk uppmätning och olika mättekniker
Erfarenhet av att självständigt driva arbete med avvikelsehantering och grundorsaksanalyser samt implementering av korrigerande åtgärder
Erfarenhet av systematiskt förbättringsarbete, t ex gnm LEAN
God förmåga att uttrycka sig i tal och skrift på svenska och engelska, men behärskar också teknisk terminologi på båda språken
Då mekaniklabbet endast består av två personer lägger vi stor vikt vid personlig lämplighet utöver de rena kvalifikationskraven



Önskvärda egenskaper:
God samarbetsförmåga
Resultat- och målinriktad
Ansvarstagande
Noggrann
Initiativrik
God problemlösningsförmåga
Orädd att arbeta i olika datasystem
Intresse för att jobba med mekanik & instrument Visa mindre

Nordic Controller

Role Summary: The Nordic Controller reporting to the EMEA Controller is responsible for ensuring that all statutory and US GAAP requirements are met across the group of legal Nordic legal entities (Norway, Sweden, Finland and Denmark). They will provide support for the Accounting Operations teams to ensure financial statement accuracy for US GAAP and Statutory Accounting and will provide guidance to local Business teams on operational and accounting matt... Visa mer
Role Summary:


The Nordic Controller reporting to the EMEA Controller is responsible for ensuring that all statutory and US GAAP requirements are met across the group of legal Nordic legal entities (Norway, Sweden, Finland and Denmark). They will provide support for the Accounting Operations teams to ensure financial statement accuracy for US GAAP and Statutory Accounting and will provide guidance to local Business teams on operational and accounting matters.


Essential Responsibilities:


Lead a team of local accounting personnel focused on Statutory and US GAAP reporting activities for the Nordic entities including a key manufacturing location.
Coordinate the Preparation of all the necessary Board of Directory meeting documents and be financial face for the presentations to the board
Build strong relationships with the Finance & Operational teams and have the necessary expertise to understand and resolve technical or operational issues in the region and engage the relevant team or CoE as required. Provides Country specific expertise and language support
Monitor and regularly review the financial ledgers of each legal entity & ensure compliance with local laws/GAPs, tax codes, government regulations and Statutory and Tax filing requirements.
Support the Accounting Operations Finance team on the annual statutory audit with EY/ KPMG for the region including SOX Audit support
Ensure appropriate sign off of audited financial statements and appropriate Board representation
Key local contact for EY/ KPMG auditor and tax authorities
Drive closure of open audit issues (both KPMG & internal audit) and proactively work to prevent future issues / manage risk. Oversee resulting corrective action process in Accounting Operations
Monitor and review that appropriate Internal Controls are in place, in line with local statutory laws and US GAAP, and critically examine potential issues where financial risks & opportunities may be drawn out
Oversee account reconciliations, KPI’s and closing activities for the region ensuring high quality and timely delivery of financial information from Accounting Operations
Proactively lead adherence to the compliance policies
Supports business changes and transformations including acquisitions / disposals
Identify potential risks and opportunities and communicate effectively to key stakeholders
Manage the fiscal budget for the Nordic Controllership team. Monitor actuals and present information to the EMEA Controller



For more information about the position please contact Jonathan Battrick: [email protected]


Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


Qualifications/Requirements:


Qualified Accountant with significant post qualification experience OR Bachelor’s degree in accounting, finance, or other business-related field and major progressive accounting or finance experience or equivalent knowledge or experience.
Fluent in English, written and spoken. Swedish language knowledge is a huge advantage
Proficiency in U.S. GAAP or another internationally recognized accounting framework and authoritative accounting literature
Proficiency in Swedish GAAP for entity structure consolidation and reporting
EU Work Permit is required



Desired Characteristics:


Integrity: accepting and adhering to high moral, ethical, and personal values in decisions, communications, actions and when dealing with others
External focus: capable of forging strong relationships with finance and non-finance leaders
Excellent verbal and written communication skills and the ability to communicate complex accounting matters clearly
Encourage teamwork & Co-operation to achieve the common aim. ”He or she is a good team player”.
Clear thinker / problem solver: successfully led projects/process improvements within operations/finance functions; able to quickly grasp new ideas
Strong analytical skills: able to clearly link financial results to operational performance drivers, generate alternatives and drive positive change
Adaptable/Flexible: being open to change in response to new information and in different or unexpected circumstances
Proficient use of financial systems Visa mindre

HR Coordinator

Role Summary: In this role, you will be responsible for supporting the Sweden HR team (9 HR Managers supporting approx. 2000 employees in 2 locations) in their deliveries to the business, providing dedicated support with specific focus on HR transactions, administration, data maintenance, reporting, onboarding, and more. Please apply by February 3rd. For questions, please contact HR Country Manager Christina Dahlgren (christina.dahlgre[email protected]) Essenti... Visa mer
Role Summary:
In this role, you will be responsible for supporting the Sweden HR team (9 HR Managers supporting approx. 2000 employees in 2 locations) in their deliveries to the business, providing dedicated support with specific focus on HR transactions, administration, data maintenance, reporting, onboarding, and more.


Please apply by February 3rd. For questions, please contact HR Country Manager Christina Dahlgren ([email protected])


Essential Responsibilities:
You will be responsible for executing on HR operations, including developing an in-depth understanding of relevant HR systems, processes, and policies- you will act as the “go-to” for the HR team and the managers they support. This role requires emphasis on data integrity and analysis to support key HR decisions and works cross functionally with internal teams to become a contributing member of the HR team.


Supporting the HR team in their deliveries to the business
Execute HR operations for the Sweden Biopharma business
Oracle HR/Workday management
Maintain and protect confidential data with utmost scrutiny, judgment, and care 
Assist with HR projects, events or initiatives as needed
Manage employment transactions based on defined operations processes to ensure quality delivery & compliance, including pre-onboarding & onboarding, 1st day introduction, exit process, contract renewal, internal transfer, etc
Support the business HR team with operating mechanisms
Management of union documents
Coordinate, plan and deliver New Employee Orientation Program and New Manager Introduction program
Develop strong working relationships with business HR to ensure effective communication
Lead and/or participate global, country, and Ops team-initiated projects process/ system review, employee events, etc
Respond to questions/requests from HR partners, employees and other stakeholders



Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


Qualifications/Requirements:
Some related HR operations /HR Coordination experience
Confidentiality & controllership mindset
Detail oriented and strong execution ability
Ability to anticipate and resolve challenges
High energy level with strong customer service mindset & can do attitude
Excellent interpersonal & communication skills
Project management skills
Fluent English in both verbal and written
Good command of PC skills



Desired Characteristics:
Fluency in local language and English, with professional verbal & written communication skills
Experience of a HR or Operations process ownership role in a fast-paced, customer- oriented environment within a large organization
Demonstrated organizational skills, high standard of accuracy, an attention to detail, and excellent follow-up skills
Proficient IT skills including Excel, Word and Outlook, Oracle HR, Hiresystems, Workday
Self-starter who can manage multiple tasks simultaneously with minimal supervision
Ability to anticipate and resolve challenges
Solid analytical skills including the ability to identify trends and implement process improvements
Effective interpersonal skills; proven ability to develop and maintain team and client relationships, both in immediate and remote contexts
Strong presentation and status reporting skills
Demonstrated project ownership and accountability Visa mindre

HR Coordinator

In this role, you will be responsible for supporting the Sweden HR team (9 HR Managers supporting approx. 2000 employees in 2 locations) in their deliveries to the business, providing dedicated support with specific focus on HR transactions, administration, data maintenance, reporting, onboarding, and more. Please apply by February 3rd. For questions, please contact HR Country Manager Christina Dahlgren ([email protected]) Essential Responsibilit... Visa mer
In this role, you will be responsible for supporting the Sweden HR team (9 HR Managers supporting approx. 2000 employees in 2 locations) in their deliveries to the business, providing dedicated support with specific focus on HR transactions, administration, data maintenance, reporting, onboarding, and more.
Please apply by February 3rd. For questions, please contact HR Country Manager Christina Dahlgren ([email protected])


Essential Responsibilities:
You will be responsible for executing on HR operations, including developing an in-depth understanding of relevant HR systems, processes, and policies- you will act as the “go-to” for the HR team and the managers they support. This role requires emphasis on data integrity and analysis to support key HR decisions and works cross functionally with internal teams to become a contributing member of the HR team.
Supporting the HR team in their deliveries to the business
Execute HR operations for the Sweden Biopharma business
Oracle HR/Workday management
Maintain and protect confidential data with utmost scrutiny, judgment, and care 
Assist with HR projects, events or initiatives as needed
Manage employment transactions based on defined operations processes to ensure quality delivery & compliance, including pre-onboarding & onboarding, 1st day introduction, exit process, contract renewal, internal transfer, etc
Support the business HR team with operating mechanisms
Management of union documents
Coordinate, plan and deliver New Employee Orientation Program and New Manager Introduction program
Develop strong working relationships with business HR to ensure effective communication
Lead and/or participate global, country, and Ops team-initiated projects process/ system review, employee events, etc
Respond to questions/requests from HR partners, employees and other stakeholders



Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


Qualifications/Requirements:
Some related HR operations /HR Coordination experience
Confidentiality & controllership mindset
Detail oriented and strong execution ability
Ability to anticipate and resolve challenges
High energy level with strong customer service mindset & can do attitude
Excellent interpersonal & communication skills
Project management skills
Fluent English in both verbal and written
Good command of PC skills



Desired Characteristics:
Fluency in local language and English, with professional verbal & written communication skills
Experience of a HR or Operations process ownership role in a fast-paced, customer- oriented environment within a large organization
Demonstrated organizational skills, high standard of accuracy, an attention to detail, and excellent follow-up skills
Proficient IT skills including Excel, Word and Outlook, Oracle HR, Hiresystems, Workday
Self-starter who can manage multiple tasks simultaneously with minimal supervision
Ability to anticipate and resolve challenges
Solid analytical skills including the ability to identify trends and implement process improvements
Effective interpersonal skills; proven ability to develop and maintain team and client relationships, both in immediate and remote contexts
Strong presentation and status reporting skills
Demonstrated project ownership and accountability Visa mindre

Global Privacy Leader

Role Summary: This role provides policy, regulatory & legal/compliance leadership and support on global privacy matters (particularly US, EU and China) for the Biopharma business and will be responsible for setting up and driving the overall global privacy program including providing expert advice, investigating potential issues, monitoring legal developments and leading projects to improve data protection. Preferred location are either Marlborough (US), U... Visa mer
Role Summary:
This role provides policy, regulatory & legal/compliance leadership and support on global privacy matters (particularly US, EU and China) for the Biopharma business and will be responsible for setting up and driving the overall global privacy program including providing expert advice, investigating potential issues, monitoring legal developments and leading projects to improve data protection. Preferred location are either Marlborough (US), Uppsala (Sweden) or Amersham (UK).
Essential Responsibilities:
• Provides expert advice on healthcare, customer and employee privacy laws and regulations, with a particular emphasis on the EU General Data Protection Regulation 2016/679 (GDPR), the Health Insurance Portability and Accountability Act of 1996 (HIPAA), and related implementing rules and regulations.
• Serves as a subject matter expert and resource by fielding and addressing inquiries from employees, and provide support in contract negotiations regarding data.
• Works cross-functionally to investigate and resolve individual privacy compliance issues, customer complaints, misuse of data, and data breaches by assessing causes, developing corrective actions, and ensuring consistent application of corrective actions.
• Monitors legal developments and enforcement activities globally: pro-actively assess the risk profile with respect to compliance with data protection laws and policies and develops appropriate measures to address and mitigate the identified risks; develops key strategies, and implements actions vis-à-vis privacy institutions and regulatory agencies in a wider range of areas.
• Develop and maintain privacy and data protection compliance framework scorecard and metrics.
• Conducts periodic and as-needed business audits and risk assessments to assess data privacy and security compliance.
• Collaborates with development teams to ensure that new introductions or versions of products and services comply with applicable data privacy and security requirements (legal, contractual or otherwise), and assists in the negotiation of data privacy and security provisions in related contracts/agreements.
• Manage outside counsel or other third-party adviser where brought to assist.
• Organize filings with data protection authorities, review and track them on a regular basis.
• Draft and/or advise on data protection policies, issue guidelines and procedures on data privacy as required, provide privacy compliance training and periodic best practices reminders to assigned business teams.


All GE employees may be considered for this role. Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of the transaction.


Qualifications/Requirements:
• Significant years of working experience at a large law firm, corporate legal department or in equivalent compliance function, with significant experience in healthcare privacy matters.
• Deep knowledge of EU and US privacy laws, regulations and best practices, with particular experience in the healthcare industry.
• Proven track record of project and process development, implementation and project management, with minimal supervision required.
• Proven ability to function as a member of a global team in a complex, matrix environment.
• Demonstrated experience identifying and resolving legal and regulatory issues quickly and effectively, with an ability to make real-time decisions.
• Candidate must be highly organized, computer literate, a self-starter, and good at managing and prioritizing numerous projects to meet demanding deadlines.
• Candidate should be comfortable working with senior managers and have the ability to understand commercial and financial drivers.
• Strong communication and interpersonal skills.
Desired Characteristics:
• Alternatively, experience in information security, privacy program management.
• Level-headed approach to risk and managing such risk against business objectives.
• High level of energy and the ability to pass it on to other team members.
• Executive influencing, clear & concise communication and presentation skills.
• Experience conducting internal audits.
• Experience with Training and course development.
• Familiar with Continuous Improvement methodologies, including Lean/Six Sigma.
• Familiar with Nymity software or similar Visa mindre

Processoperatörer till Lösningsmedelsåtervinningen på GE Healthcare

Vill du vara med och leverera lösningsmedel till produktionsenheter som tillverkar eftertraktade produkter som hjälper diabetes- och cancerpatienter runt om i världen? Vill du vara del av ett starkt team där du kan påverka din vardag på jobbet? Vill du ha ett varierande arbete i en expanderande verksamhet där du får arbeta fysiskt men även utvecklas med högteknologiska lösningar? Är du en engagerad och nyfiken person som letar efter utmaningar? Då kan du v... Visa mer
Vill du vara med och leverera lösningsmedel till produktionsenheter som tillverkar eftertraktade produkter som hjälper diabetes- och cancerpatienter runt om i världen? Vill du vara del av ett starkt team där du kan påverka din vardag på jobbet? Vill du ha ett varierande arbete i en expanderande verksamhet där du får arbeta fysiskt men även utvecklas med högteknologiska lösningar? Är du en engagerad och nyfiken person som letar efter utmaningar? Då kan du vara den nya medarbetare som vi söker!


Vi söker nu två processoperatörer till sektionen Lösningsmedelsåtervinningen, inom Kemisk produktion i Uppsala. Inom sektionen är vi idag en grupp på 1 chef, 3 ingenjörer, 1 samordnare och 14 operatörer som försörjer den storskaliga produktionen med lösningsmedel genom återvinning ur moderlutar och lossning av tankbilar.
Tjänsterna är vikariat tom 2021-09 och tillsättes snarast. En operatör kommer att arbeta 2-skift och en 3-skift.


Huvudsakliga arbetsuppgifter:
Sektionen Lösningsmedelsåtervinningen ansvarar för ett fabriksavsnitt, C7 och två tankgårdar med tillhörande lossningsstation för tankbilar. Tillverkningen sker med hög automationsgrad, där styrsystem 800xA och batchprotokoll används dagligen. Operatörsarbetet präglas av variation och en möjlighet till att påverka den dagliga verksamheten, där återvinningsprocesserna är i fokus men det självständiga förbättringsarbetet fortgår under tiden. En ny byggnad (C8) med processutrustning är under uppförande och ska driftsättas under H1 2020.


Som operatör kommer du i första hand att arbeta med:
Avdrivning och destillation av moderlut till rent lösningsmedel
Planera den dagliga verksamheten med avseende på lösningsmedel och tanknivåer
Mottagning av renvaror (lösningsmedel via tankbil) och utlastning av lösningsmedelsrester
Utföra daglig rondering
Utföra saneringar på rörsystem och anläggning, ingå i saneringsgruppen
Utföra provtagningar och analyser
Övervaka processer, tankar och rörsystem
Delta i EHS-relaterande ärenden
Godkänna/frisläppa lösningsmedel
Skriva arbetstillstånd och tillstånd för heta arbeten (efter utbildning)

Nästan hela LÅVs arbetsområde är Ex-klassat och vi hanterar stora mängder lösningsmedel varför du även kommer att arbeta mycket med processäkerhet.


Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


Kvalifikationer:
Gymnasium: kemi/teknisk inriktning (eller motsvarande). Kan även ha arbetat sig till motsvarande kompetens.
Erfarenhet av processindustri, arbetat efter faställda metoder
Erfarenhet av kemikaliehantering och/eller brandfarliga varor (Ex-klassning)
Goda kunskaper i att tala och skriva svenska och engelska
Högt kundfokus



Vi ser gärna att du:
Har erfarenhet av destillationer eller liknande processer
Har vana att arbeta med pumpar, ventiler etc
Har erfarenhet av styrsystem eller övervakning av processer
Tekniskt intresse och erfarenhet gällande förebyggande och avhjälpande underhåll
Är datorvan och trygg i IT-miljö (generell förståelse för Excel, Outlook etc)



Vi söker dig som är engagerad och gärna arbetar i lag. Du är nyfiken, lättlärd och inspireras av utmaningar! Som person är du säkerhetsmedveten, noggrann och mån om att alltid leverera bästa kvalitet i tid till kunden. Visa mindre

Research Engineer

We are looking for a Research Engineer, experienced in bacterial cell culture, fermentation and process development, to join our creative and collaborative team, within the Sensor Technologies section, BioProcess R&D. Our mission is to develop reagents, consumables, processes and services to support effective and reproducible processes for getting a biologics drug to the market. You will be part of a team optimizing start-to-finish processes for bioprocess... Visa mer
We are looking for a Research Engineer, experienced in bacterial cell culture, fermentation and process development, to join our creative and collaborative team, within the Sensor Technologies section, BioProcess R&D. Our mission is to develop reagents, consumables, processes and services to support effective and reproducible processes for getting a biologics drug to the market. You will be part of a team optimizing start-to-finish processes for bioprocess industry.


Essential Responsibilities:
· Design, perform, analyze, document and present bioreactor fermentation of recombinant proteins in different formats, from lab scale to bioreactors
· Develop, invent and improve new products and processes for the bioprocess industry, specifically within the fields of affinity ligands. To independently or in a team plan and accomplish given tasks from Project Manager or Section Manager, to reach given project objectives. Report accomplished tasks in writing (e.g. Technical Report) or orally
· Provide technical expertise within the areas of bacterial fermentation and process development of recombinant proteins and solve technical problems, supporting both internal production and customers
· Act as team member or Design responsible in NPI and Market Support projects
· Present scientific and technical results internally, oral and written communication in Swedish and English
· Occasional work on weekends may occur


For questions, please contact hiring manager Helena Vesterberg, e-mail: [email protected]
Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


Qualifications/Requirements:
· Bachelor or Master degree in biology, medicine, engineering or related Life Science field or equal experience in related fields or equivalent knowledge or experience.
· In order to succeed in this position you need to be 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, plan, perform, analyze, document and present results to progress our projects forward.


Desired Characteristics:
· Experience from industrial development/ R&D within medicine, biotechnology or bioprocess is a plus
· Experience in bacterial cell culturing in different formats, including bioreactor cultivation, experience in industrial scale microbial cultivation is a plus
· Experience in culture and process development for production of recombinant proteins is a plus


· Experience in different analytical techniques is a plus Visa mindre

System Engineer - tidsbegränsad anställning

Vi söker en Senior System Engineer till sektionen Instrument Engineering inom avdelningen Downstream System, R&D i Uppsala. Avdelningen Downstream Systems utvecklar bland annat instrument och mjukvara för vätskekromatografi (ÄKTA system och UNICORN) för att stödja kundernas arbetsflöden inom Bioprocess-området. Avdelningen består av många olika kompetenser såsom mekanik, elektronik, system och applikation, och arbetar i nära samarbete med mjukvaruavdelning... Visa mer
Vi söker en Senior System Engineer till sektionen Instrument Engineering inom avdelningen Downstream System, R&D i Uppsala.
Avdelningen Downstream Systems utvecklar bland annat instrument och mjukvara för vätskekromatografi (ÄKTA system och UNICORN) för att stödja kundernas arbetsflöden inom Bioprocess-området. Avdelningen består av många olika kompetenser såsom mekanik, elektronik, system och applikation, och arbetar i nära samarbete med mjukvaruavdelningen Downstream Software.


Om rollen:
Utvecklingen drivs i tvärfunktionella, ofta globala projektteam där vi tar fram produkter för Life Sciences industrin och akademin. Sektionen Instrument Engineering’s huvudfokus är hårdvaruarkitektur, koordinering av hårdvaruutveckling samt kravställning och verifiering ur ett subsystem och systemperspektiv.
Arbetsppgifter inkluderar:
Som en del av ett team, planera och leverera teamets åtaganden
Skapa användar- och systemkrav för hårdvara/mjukvara och procedurer för hur de ska verifieras
Planera, utföra och rapportera resultat från verifiering och validering av system- eller subsystemkrav
Jobba med och stötta hårdvaru/mjukvaruutvecklare inom systemutvecklingsaktiviteter
Kontinuerligt förbättra våra arbetssätt

Ditt huvudfokus kommer att vara att aktivt bidra i leveransen av nya produkter till marknaden och våra kunder.
Tidsbegränsad tjänst om 12 månader, beräknat startdatum 3 februari 2020.
För frågor, vänligen kontakta rekryterande chef: George Glosemeyer, tel. 070 612 98 65 eller [email protected]


Sökanden bör notera att denna roll kommer att ligga inom ramen för den föreslagna övergången av GE Biopharma till Danaher och kommer att övergå till Danaher när denna transaktion slutförs.
Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


Kvalifikationer:
MSc eller BSc inom Teknisk Fysik /Bioteknik/Kemiteknik eller liknande or equivalent knowledge or experience
Dokumenterad erfarenhet av produktutvecklingsarbete
Teoretisk kunskap och helst praktisk erfarenhet av proteinrening och olika applikationer
Ett genuint intresse av produktutveckling från användarens perspektiv, med fokus på att ta fram krav och ”hands-on” verifieringsaktiviteter
Strukturerad och organiserad lagspelare
Förmåga att hantera koordineringsansvar
Utmärkta kommunikations- och presentationskunskaper (både skriftliga och muntliga)
Svenska och engelska som arbetsspråk



Önskvärda egenskaper:
Förmågan att snabbt lära dig nya områden/verktyg/tekniker och arbeta som den enda representanten från sektion i olika projekt/uppgifter
Erfarenhet från arbete i tvärvetenskapliga miljöer
Resultat- och kvalitetsorienterad
Förmågan att arbeta självständigt men även tillsammans med andra
Praktisk erfarenhet av ÄKTA Platformen och UNICORN Visa mindre

Laboratoriespecialist

Vi söker en laboratoriespecialist till Quality Control i Uppsala. Avdelningen Quality Control (QC) arbetar med att kvalitetskontrollera produkter från vår produktion i Uppsala. Huvudsakliga arbetsuppgifter: I rollen som laboratoriespecialist arbetar du främst med att analysera produkter enligt gällande instruktioner och rutiner samt bedöma analysstatus. Du arbetar också med att starta och driva undersökningar vid avvikande analysresultat, utföra kalibrer... Visa mer
Vi söker en laboratoriespecialist till Quality Control i Uppsala.
Avdelningen Quality Control (QC) arbetar med att kvalitetskontrollera produkter från vår produktion i Uppsala.


Huvudsakliga arbetsuppgifter:
I rollen som laboratoriespecialist arbetar du främst med att analysera produkter enligt gällande instruktioner och rutiner samt bedöma analysstatus. Du arbetar också med att starta och driva undersökningar vid avvikande analysresultat, utföra kalibreringar och underhåll av analysinstrument samt uppdatera och godkänna arbetsinstruktioner.


Utföra analyser enligt gällande instruktioner
Avrapportera, kontrollgranska och utföra analysacceptans på produkter och uppdragsanalyser
Starta och driva undersökningar vid avvikande analysresultat och andra avvikelser
Utföra kontroller, kalibreringar och underhåll av analysinstrument
Uppdatera och godkänna arbetsinstruktioner (kontrollmetoder, standardmetoder och kalibreringsmetoder)



Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


Kvalifikationer:
Lämplig bakgrund är högskoleingenjör/gymnasieingenjör inom Kemi/Analytisk kemi/Biokemi eller liknande.


Vi söker dig som är:
noggrann och strukturerad
flexibel
bra på att samarbeta
positiv samt uppmuntrar och inspirerar andra

Vi vill också att du har förmåga att utföra flera olika arbetsuppgifter parallellt, gillar att arbeta i förändring och att driva förändringsarbete.


Önskvärda egenskaper:
Tidigare erfarenhet av laborativt kvalitetsarbete inom QC-verksamhet, gärna inom kromatografi
Datorvana MS office
Erfarenhet från arbete med Lean
Svenska och engelska i både tal och skrift Visa mindre

Processoperatör till kolonnproduktionen

Vi söker 1 processoperatörer till kolonnproduktionen, som är en del av kemisk produktion inom GE Healthcare i Uppsala. Vår sektion består av 14 personer som producerar kromatografikolonner av olika storlekar (montering, fyllning, testning, förpackning och granskning/frisläppning). Den vi söker kommer främst att höra till produktion av kolonner för användning i processskala, vilket är ett växande och spännande område.Tjänsten är tillsvidare. Huvudsakliga ... Visa mer
Vi söker 1 processoperatörer till kolonnproduktionen, som är en del av kemisk produktion inom GE Healthcare i Uppsala. Vår sektion består av 14 personer som producerar kromatografikolonner av olika storlekar (montering, fyllning, testning, förpackning och granskning/frisläppning). Den vi söker kommer främst att höra till produktion av kolonner för användning i processskala, vilket är ett växande och spännande område.Tjänsten är tillsvidare.


Huvudsakliga arbetsuppgifter:
Batchvis tillverkning enligt gällande metoder, operatörerna utför och ansvarar självstädigt för alla moment i sin produktionbatch.
Testning (kvalitetskontroll) och utvärdering av kolonnerna (görs direkt i samband med tillverkningen)
Dokumentation av tillverkning och testning i batchprotokoll och i datasystem.
Optimering av tillverkningen inom de gränser som finns angivna i instruktionerna.
Felsökning vid produktionsproblem
Uppmärksamma kvalitetsproblem och rapportera dem
Uppdatera instruktioner vid ändringar.



Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


Kvalifikationer:
Önskvärd utbildning är tex något av följande; gymnasieutbildning inom naturvetenskap/teknik, högskoleingenjör, KY-utbildning processoperatör
Du behärskar svenska flytande i tal och skrift
Du förstår engelska
Du är noggrann
Du är flexibel
Du kan arbeta självständigt
Officepaketet-goda kunskaper



Önskvärda egenskaper:
Tidigare erfarenhet av tillverkning eller kvalitetskontroll är en fördel
Tidigare erfarenhet av tillverkning i renrum är en fördel
Du kan ta egna initiativ samt fatta beslut i överenskommelse med chef och/eller kollegor.
Du har lätt för att samarbeta och ingå i team.
En fördel om du har tekniskt intresse och vill veta hur saker fungerar.
Det är ett plus om du har lätt för att kommunicera i både tal och skrift
Du bör förstå vikten av att hålla upprättad plan och kritiska leveranstider Visa mindre

Laboratoriespecialist

Vi söker en laboratoriespecialist till QC. Avdelningen Quality Control arbetar med att analysera och kvalitetskontrollera vår produktion inom Chemical Production Uppsala (CPU). Huvudsakliga arbetsuppgifter: I rollen som laboratoriespecialist arbetar du främst med att kvalitetskontrollera produkter enligt gällande instruktioner och rutiner samt bedöma om analysstatus Avrapportera, kontrollgranska och utföra analysacceptans på produkter och uppdragsanalyse... Visa mer
Vi söker en laboratoriespecialist till QC.
Avdelningen Quality Control arbetar med att analysera och kvalitetskontrollera vår produktion inom Chemical Production Uppsala (CPU).


Huvudsakliga arbetsuppgifter:
I rollen som laboratoriespecialist arbetar du främst med att kvalitetskontrollera produkter enligt gällande instruktioner och rutiner samt bedöma om analysstatus
Avrapportera, kontrollgranska och utföra analysacceptans på produkter och uppdragsanalyser
Starta och driva undersökningar vid avvikande analysresultat och andra avvikelser
Utföra kontroller, kalibreringar och underhåll av analysinstrument
Uppdatera och godkänna arbetsinstruktioner (kontrollmetoder, standardmetoder och kalibreringsmetoder)
Analysera och avrapportera analysresultat inom överenskomna ledtider.
I samband med analysacceptans följa analysmetoders prestanda genom trendning.
Arbeta för att hålla metoder och instrument/utrustningar funktionsdugliga och tillförlitliga.
Säkerställa att instrument och utrustningar är kvalificerade och har tillräcklig nivå på kontroll, kalibrering och underhåll.
Öppna och utreda avvikande analysresultat.



Kvalifikationer:
Lämplig bakgrund är högskoleingenjör/ gymnasieingenjör inom Kemi/Analytisk Kemi/ Biokemi eller liknande.


Vi söker någon som är:
noggrann och strukturerad
flexibel
bra på att samarbeta
positiv, uppmuntrar och inspirerar andra
stresstålig och kan utföra flera olika arbetsuppgifter parallellt
gillar att arbeta i förändring och driva förändringsarbete



Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


Önskvärda egenskaper:
Tidigare erfarenhet av laborativt kvalitetsarbete inom QC-verksamhet, gärna inom kromatografi
Datorvana MS Office
Protein-kemi Visa mindre

Contractor Safety Coordinator/ byggarbetsmiljösamordnare (BasP/U)

GE Healthcare bedriver över tiden ett mycket stort antal projekt. Vi har ett stort fokus på att utveckla nya produkter, förbättra processer och att öka kapaciteten. Vi är en stor och komplex site och med den utmaningen att underhålla och utveckla fastigheter och processer för att säkerställa en fortsatt hög lönsamhet och god arbetsmiljö. Detta förutsätter en omfattande samordning av projekt och entreprenörer för att säkerställa ett optimerat nyttjande av r... Visa mer
GE Healthcare bedriver över tiden ett mycket stort antal projekt. Vi har ett stort fokus på att utveckla nya produkter, förbättra processer och att öka kapaciteten. Vi är en stor och komplex site och med den utmaningen att underhålla och utveckla fastigheter och processer för att säkerställa en fortsatt hög lönsamhet och god arbetsmiljö. Detta förutsätter en omfattande samordning av projekt och entreprenörer för att säkerställa ett optimerat nyttjande av resurser samt en god arbetsmiljösäkerhet.


Huvudsakliga arbetsuppgifter:
Vi söker därför en kvalificerad och erfaren byggarbetsmiljösamordnare (BasP/U) för koordinering av arbetsmiljösäkerhet i våra projekt och med ansvar att koordinera verksamheten mellan våra projekt. Vi söker dig som har förmågan att vara ”spindeln i nätet” och skapa förutsättningar för att projektledare, byggarbetsmiljösamordnare, entreprenörer ska lyckas!
Du kommer att ingå i Real Estate men arbeta mycket nära såväl PM (Project Management) och EHS (Environment, Health and Safety). 
Fokus är arbetsmiljösäkerhet, efterlevnad av lagstiftning och regelverk samt att stödja våra projektledare, entreprenörer och byggarbetsmiljösamordnare. Då vi bedriver många olika projekt samtidigt har vi ett stort behov av att samordning. 
• En central del av arbetet består i att på plats följa de olika projekten för att säkerställa kommunikation och samarbete och att tydliggöra för entreprenörer och byggarbetsmiljösamordnare vilka regler som GE ställer inom arbetsmiljö.
• Du kommer även att delta i upphandlingar av entreprenörer och följa upp deras Systematiska Arbetsmiljöarbete (SAM). 
• En del i ditt arbete är att delta i projektens skyddsronder och HKI (House keeping inspections).


Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


Kvalifiktioner: 
Du är utbildad och certifierad byggarbetsmiljösamordnare och har en omfattande och dokumenterad erfarenhet från byggprojekt inom industri.
Du är välbekant med säkerhetspraxis, analysmetoder och regelverk inom området samt känner dig bekväm med att arbeta med och tolk lagtexter.
Erfarenhet från Sevesoklassade industrier och läkemedels- och medicintekniska industrier är meriterande.
Du har även kunskap och erfarenhet av riskhanteringsmetodik och olycksutredningsmetodik.
Du måste tycka om att hjälpa andra och även våga säga nej när säkerheten kräver det.
Du behöver erfarenhet av att skriva och uppdatera styrande rutiner och dokument samt att implementera detsamma.
Som person är du organiserad och strukturerad med god förmåga att förklara och förankra dina beslut.
Du jobbar i en supportfunktion där det är viktigt att ha ett övergripande perspektiv där du bedriver ett framåtsyftande förbättringsarbete, bland annat genom att skapa möjlighet till utbildning.
Du arbetar mycket självständigt, är initiativtagande och uppskattar samverkan med andra. Du har god problemlösningsförmåga. Du är en god lyssnare och kommunikatör som visar engagemang. Du är positiv till förändrings- och förenklingsarbete.
Du uttrycker dig obehindrat både muntligt och skriftligt på svenska och engelska och har datorvana. Visa mindre

Talent Acquisition Specialist

Role Summary: You will be responsible for providing wing to wing recruitment support and activity to the Biopharma business predominantly in Sweden, but where needed also for selected roles in Europe, predominantly a mix of external hires, internal moves and contractor conversions. This is a great opportunity for an HR or TA professional who would like to grow his or her career in Talent Acquisition area and is eager to join Biopharma’s unique journey of b... Visa mer
Role Summary:
You will be responsible for providing wing to wing recruitment support and activity to the Biopharma business predominantly in Sweden, but where needed also for selected roles in Europe, predominantly a mix of external hires, internal moves and contractor conversions. This is a great opportunity for an HR or TA professional who would like to grow his or her career in Talent Acquisition area and is eager to join Biopharma’s unique journey of building its own TA function.


Essential Responsibilities:
• Manage ‘wing to wing’ recruiting activity, predominantly a mix of external hires, internal moves and contractor conversions.
• Stakeholders include specific Hiring Managers, relevant HR counterparts, HR Operations and all candidates
• Create attractive & compliant external job postings
• Conduct job launch meeting with Hiring Managers, set process & communication expectations
• Utilize sourcing channel, leverage job boards and social media
• Use active candidate pipeline to identify top talent for your specific job requisitions and track through Applicant Tracking System (ATS)
• Collect required documentation for screening
• Interview and evaluate candidates to qualify them for the role, in person or via phone
• Qualify candidates using the available job description information, references, technical screens and test sources
• Be capable of managing the verbal offer process
• Coach managers/interview teams to incorporate capability/competency based assessments during their interview
• Monitor performance metrics. Understand Business targets & personal performance
• Help support Biopharma’s diversity initiatives & strategy to attract a diverse workforce to the company
• Ensure Local country knowledge of staffing & process compliance is followed
• Learn about & understand your business/function/region
• Able to join TA led projects, provide input, act as Subject Matter Expert in process-driven projects and move forward on actions allocated


Please reach out to Andreas Johansson, Talent Acquisition Sweden, in case of any questions related to this opening.


All GE employees may be considered for this role. Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction. #CR


Qualifications/Requirements:


• Bachelor’s Degree and a few years of experience in recruiting
• Fluency in English and Swedish, another European language is a plus
• Experience in using Applicant Tracking Systems (ATS) to track and manage interview slates
• Experience from Candidate Relationship Management (CRM) tools for candidate pipelining as well as LinkedIn for candidate searches is an advantage


Desired Characteristics:


Technical Expertise:
• Seeks to understand the need for recruiting subject matter domain expertise.
• Seeks understanding of sourcing processes and techniques, utilizes boolean searches in order to find passive candidates.
• Creates a basic list of passive and qualified leads.


Personal Attributes:
• Builds rapport and relationships with peers, recognizes how confidence and assertiveness help in completing tasks/projects.
• Exemplifies a positive attitude and act as a brand ambassador.
• Articulates opinions and presents clear rationale, receives feedback in a constructive and positive way.
• Great sense of urgency Visa mindre

European Patent Attorney

Role Summary: Reporting to a more senior GE Biopharma IP Counsel, this role will provide an opportunity to work with a cross-functional team on specific aspects of patent strategy across GE’s Biopharma business. The successful candidate will be responsible for drafting patent applications and prosecuting a global patent portfolio, including acting as the European representative before the European Patent Office for European applications. Essential Respon... Visa mer
Role Summary:
Reporting to a more senior GE Biopharma IP Counsel, this role will provide an opportunity to work with a cross-functional team on specific aspects of patent strategy across GE’s Biopharma business. The successful candidate will be responsible for drafting patent applications and prosecuting a global patent portfolio, including acting as the European representative before the European Patent Office for European applications.


Essential Responsibilities:
This role will also encompass:
general IP counseling
managing idea generation
opposition work
freedom-to-operate reviews
licensing and enforcement


All GE employees may be considered for this role. Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


Qualifications/Requirements:
European Patent Attorney.
Technical background in electrical, chemical or mechanical engineering, software, physics or equivalent.
Excellent written and oral communication skills.
Capable of devising innovative IP strategies


Desired Characteristics:
Knowledge of laws, regulations, practices and procedures relating to patent procurement in Europe, US and Asia.
Technical experience working in the life sciences or healthcare sector, advantageously: in bioprocessing; fluidic; and/or electromechanical control fields.
Experience acting as European representative before the European Patent Office.
Experience prioritizing competing demands to make real time decisions/recommendations in a fast-paced environment.
Demonstrated ability to quickly identify & prioritize issues, develop process-driven solutions, and effectively communicate with a wide range of people. Visa mindre

Lead- Supplier Quality Engineer

The Supplier Quality Engineer is responsible for driving exceptional product quality for the patient safety, customer value beyond expectations, regulatory assurance, and optimized Cost of Quality for GEHC. This is a key technical position, affecting part quality. The position reports into a global team and will be supporting the Uppsala and other GEHC Life Sciences sites, as required. Essential Responsibilities: Improve supplier quality performance for ... Visa mer
The Supplier Quality Engineer is responsible for driving exceptional product quality for the patient safety, customer value beyond expectations, regulatory assurance, and optimized Cost of Quality for GEHC. This is a key technical position, affecting part quality. The position reports into a global team and will be supporting the Uppsala and other GEHC Life Sciences sites, as required.


Essential Responsibilities:
Improve supplier quality performance for assigned suppliers via Quality and Plan implementation.
Approve supplier selection through robust qualification processes.
Drive site implementation of the GEHC QMS for interface processes relevant to Supplier Quality.
Assure supplier compliance to GEHC QMS and regulatory requirements through supplier monitoring process.
Develop positive relationships and work closely with Global Sourcing, Manufacturing, Engineering and QA to manage and implement supplier/engineering changes, New Product Introductions and Transfers.
Interface with Suppliers, Engineering, Service, Manufacturing and Sourcing to drive Quality improvements that minimize the Costs of Quality.
Assure Corrective and Preventive Action plans are developed and executed at assigned suppliers in compliance with the CAPA process.
Demonstrated ability to lead, acknowledge, develop, communicate & implement a strategy to ensure compliance.
Develop and execute on Supplier Audit Plan.



Quality Specific Goals:
Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position.
Complete all planned Quality & Compliance training within the defined deadlines.
Identify and report any quality or compliance concerns and take immediate corrective action as required.
Knowledge and understanding of GEHC Purchasing Controls Procedure and associated Work Instructions and operates within them to ensure that all purchased product and services conform to specified requirements.
Ensure a compliant and qualified supply base by conducting supplier evaluations.
Develop the GEHC Purchasing Controls Procedure and continuously improve Work Instructions, Templates and Procedures.



Qualifications/Requirements:
Degree in an engineering or technical discipline or equivalent non-technical degree with experience in manufacturing, engineering or quality assurance or equivalent knowledge or experience.
Experience in supplier quality engineering, quality assurance, quality engineering, manufacturing, or engineering.
Quality auditing experience
Proficiency with Microsoft Excel spreadsheet development and database analysis.
Effective problem solving, root-cause analytical skills to lead and influence others to drive change (cross-functionally and globally).
Demonstrated knowledge of Quality Management System tools, continuous improvement methodologies and in-depth understanding of site level products and related processes.
Able to use English as working language.



Desired Characteristics:
Ability to effectively communicate within all levels of the organization.
Trained Supplier Quality Auditor
Expertise in Industrial Manufacturing Processes.
Experience of Calibration and Software suppliers.
Demonstrated collaboration, negotiation & conflict resolution skills.
Excellent oral communication & report, business correspondence & procedure-writing skills.
Supplier quality management experience Visa mindre

UNICORN Product Manager

This position is accountable for the competitiveness of UNICORN in terms of features, functionality, and quality. This role will provide the strategic direction for UNICORN, product positioning, and focusing on the specific business needs of the customer. The Product Manager will help to drive the growth, competitiveness, and long-term adoption of UNICORN. The Product Manager works with stakeholders, internal teams, customers, and helps in the formation o... Visa mer
This position is accountable for the competitiveness of UNICORN in terms of features, functionality, and quality. This role will provide the strategic direction for UNICORN, product positioning, and focusing on the specific business needs of the customer.
The Product Manager will help to drive the growth, competitiveness, and long-term adoption of UNICORN. The Product Manager works with stakeholders, internal teams, customers, and helps in the formation of the strategic roadmap of UNICORN.




Essential Responsibilities:
The role requires a deep understanding of the customer’s environment, competitor products, and overall market trends. The product manager is the source of decisions around our software solution, vision, strategy, and roadmaps of our products.

Key responsibilities include:
Training sales modalities and Pricing the product
Profit, Loss, and Margin
Number of units sold
Year over Year growth in units and revenue
Working with marketing, engineering, and services on long-term product roadmaps, requirements, and business plans.
Driving the product portfolio to meet the needs of the market. Responsible for strategy and execution of the product roadmaps and new product introductions.
Work closely with engineering to ensure at each step of development intent and goals are continually met.
Ensuring the “voice of the customer” is reflected in products by working with and building partnerships with customers as required.
Managing key business financial performance indicators (including cost, margin, unit sold, % increase) and continual improvement of products.
Close collaboration with marketing to translate customer needs, market analysis, competitive analysis, and regulatory environment factors into actionable strategies and tactics for the product.
Partner with internal and external domain experts to highlight emerging practice trends and product/content needs of the customer.
Conducting product research to further understand the competitive profile for the segment worldwide (where applicable) and opportunities for growth.
Establish tradeoffs between internal development and business partnership activities with strategic partners-including contract negotiations and maintenance, product changes, forecasting and financials.
Coordinating product requirements across a multi-functional organization, including marketing, sales, operations, engineering, and services teams, while ensuring compliance with quality systems and regulatory requirements.
Evangelize for the product by presenting to customers and users groups; represent the product at trade shows and with media; sell product roadmap internally; participate in winning large deals; provide sales training, and generate enthusiasm for the product.
Partner with engineering, enterprise and customer service to successfully meet customer expectations in product delivery and quality.
In collaboration with marketing identify the marketplace and customers based on the customers business (Big, medium, small pharma) as well as where in the product development the customers are (research, process development or manufacturing).
Coordinate and drive the solution architectural requirements for the product and ensuring a clear road map for the architecture is maintained and communicated.
Communicate and align with the appropriate hardware product managers to ensure unit requriemnts as well as solutions requriments are met.


Please contact Chris Sandusky for more information regarding the position +1 508 573 0012 email: [email protected]
Last day to apply is December 15th.


Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.
 
Qualifications/Requirements:
Bachelor’s Degree in Electrical Engineering, Chemical Engineering, Automation engineering or similar field or equivalent knowledge or experience.
Significant experience in Product management, product development, or related field including workflow experience with similar products.
Excellent oral and written communications skills
Strong analytical and process skills
Strong project management skills
Ability to work effectively within a matrix environment



Desired Characteristics:
 Major experience in the software industry, product development or related field.
Deep Product Management/Marketing expertise, including: market trends/analysis, NPI process, product roadmap development, requirements, product life-cycle management,
 Understanding of software as a service and how to implement this offering.
Software product/industry/technical acumen
Leadership skills to lead teams and shape/lead growth vision and marketing strategy
Innovation – develop new ideas through collaboration and execute on creative ideas
Team oriented – ability to motivate and work well with diverse, cross-functional teams
Proven ability to work globally
Proven ability to influence and negotiate internally and with customers. Visa mindre

Senior System Engineer - temporary assignment

Vi söker en Senior System Engineer till sektionen Instrument Engineering inom avdelningen Downstream System, R&D i Uppsala. Avdelningen Downstream Systems utvecklar bland annat instrument och mjukvara för vätskekromatografi (ÄKTA system och UNICORN) för att stödja kundernas arbetsflöden inom Bioprocess-området. Avdelningen består av många olika kompetenser såsom mekanik, elektronik, system och applikation, och arbetar i nära samarbete med mjukvaruavdelning... Visa mer
Vi söker en Senior System Engineer till sektionen Instrument Engineering inom avdelningen Downstream System, R&D i Uppsala.
Avdelningen Downstream Systems utvecklar bland annat instrument och mjukvara för vätskekromatografi (ÄKTA system och UNICORN) för att stödja kundernas arbetsflöden inom Bioprocess-området. Avdelningen består av många olika kompetenser såsom mekanik, elektronik, system och applikation, och arbetar i nära samarbete med mjukvaruavdelningen Downstream Software.


Om rollen:
Utvecklingen drivs i tvärfunktionella, ofta globala projektteam där vi tar fram produkter för Life Sciences industrin och akademin. Sektionen Instrument Engineering’s huvudfokus är hårdvaruarkitektur, koordinering av hårdvaruutveckling samt kravställning och verifiering ur ett subsystem och systemperspektiv.
Arbetsppgifter inkluderar:
Som en del av ett team, planera och leverera teamets åtaganden
Skapa användar- och systemkrav för hårdvara/mjukvara och procedurer för hur de ska verifieras
Planera, utföra och rapportera resultat från verifiering och validering av system- eller subsystemkrav
Jobba med och stötta hårdvaru/mjukvaruutvecklare inom systemutvecklingsaktiviteter
Kontinuerligt förbättra våra arbetssätt

Ditt huvudfokus kommer att vara att aktivt bidra i leveransen av nya produkter till marknaden och våra kunder.
Tidsbegränsad tjänst om 12 månader, beräknat startdatum 3 februari 2020.
För frågor, vänligen kontakta rekryterande chef: George Glosemeyer, tel. 070 612 98 65 eller [email protected]


Sökanden bör notera att denna roll kommer att ligga inom ramen för den föreslagna övergången av GE Biopharma till Danaher och kommer att övergå till Danaher när denna transaktion slutförs.
Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


Kvalifikationer:
MSc eller BSc inom Teknisk Fysik /Bioteknik/Kemiteknik eller liknande or equivalent knowledge or experience
Dokumenterad erfarenhet av produktutvecklingsarbete
Teoretisk kunskap och helst praktisk erfarenhet av proteinrening och olika applikationer
Ett genuint intresse av produktutveckling från användarens perspektiv, med fokus på att ta fram krav och ”hands-on” verifieringsaktiviteter
Strukturerad och organiserad lagspelare
Förmåga att hantera koordineringsansvar
Utmärkta kommunikations- och presentationskunskaper (både skriftliga och muntliga)
Svenska och engelska som arbetsspråk



Önskvärda egenskaper:
Förmågan att snabbt lära dig nya områden/verktyg/tekniker och arbeta som den enda representanten från sektion i olika projekt/uppgifter
Erfarenhet från arbete i tvärvetenskapliga miljöer
Resultat- och kvalitetsorienterad
Förmågan att arbeta självständigt men även tillsammans med andra
Praktisk erfarenhet av ÄKTA Platformen och UNICORN Visa mindre

Senior Electrical Engineer

Sektionen ”Hardware Engineering” består av 20 personer med kompetens inom främst mekanik och elektronik. Sektionen ingår i avdelningen “Bioprocess systems R&D” med cirka 100 personer som är indelade i sju sektioner. “Bioprocess systems R&D” utvecklar både hårdvara och mjukvara. Vi tar fram nya system, men gör även underhåll och förbättringar av befintliga system, t ex inom produktfamiljerna ÄKTA och Biacore. Essential Responsibilities: Vi söker en driven... Visa mer
Sektionen ”Hardware Engineering” består av 20 personer med kompetens inom främst mekanik och elektronik. Sektionen ingår i avdelningen “Bioprocess systems R&D” med cirka 100 personer som är indelade i sju sektioner. “Bioprocess systems R&D” utvecklar både hårdvara och mjukvara. Vi tar fram nya system, men gör även underhåll och förbättringar av befintliga system, t ex inom produktfamiljerna ÄKTA och Biacore.


Essential Responsibilities:
Vi söker en driven och ansvarsfull el- & elektronikkonstruktör som vill jobba med framtidens system för läkemedelsframtagning.
Det dagliga arbetet består i att konstruera el & elektronik för storskaliga system, ofta med krav enligt UL508 och EN60204.
Vi ser att du har erfarenhet från att konstruera elsystem med tex PLC, motordrivare, transmittrar, sensorer, kraftaggregat mm.
Det är meriterande om du har erfarenhet av utveckling med fokus på serieproduktion, tillverkningskostnad, regulatorisk testning mm.
Du ska trivas i en miljö där du får jobba och kommunicera med ett brett kontaktnät, allt från tidig konstruktion till produktion.
Arbetet innefattar att aktivt delta och driva utveckling av el- & elektroniksystem för storskaliga system. Storskaliga system används i produktionsmiljö av våra produkter.



För frågor, kontakta rekryterande chef Thomas Arctaedius på tel. 0730-455104 eller [email protected]


Qualifications/Requirements:
Högskoleingenjör
Bevisad erfarenhet från produktutveckling
Erfarenhet från el-CAD, tex Zuken E3, E-plan eller AutoCAD electrical
Flytande språkkunskaper i svenska och engelska



Desired Characteristics:
Erfarenhet av OrCAD eller liknande är ett plus Visa mindre

Post Doc- Chromatography Modeling

“mAb applications” is a section within the Downstream Resins Department (~100 people) which belong to the Global BioProcess R&D (~500 people). The section is based in Uppsala and consists of ~15 highly skilled research engineers and scientists all with a solid background in molecular biology, bioanalysis and downstream purification. Essential Responsibilities: The section is responsible for designing downstream processes for monoclonal antibodies and rel... Visa mer
“mAb applications” is a section within the Downstream Resins Department (~100 people) which belong to the Global BioProcess R&D (~500 people). The section is based in Uppsala and consists of ~15 highly skilled research engineers and scientists all with a solid background in molecular biology, bioanalysis and downstream purification.


Essential Responsibilities:
The section is responsible for designing downstream processes for monoclonal antibodies and related molecules and is also contributing to the development of new resins based on structure function relationships. Statistical modelling together with deep chromatographic understanding are two cornerstones in our daily work.
We are now looking for an experienced person that can contribute to our development of multimodal ligands. We are seeking a chromatography modeling Post Doc to join our entrepreneurial team for development of an iterative approach to explorative ligand selectivity maturation.
Generation of descriptive chromatographic data and mechanistic modeling applied to directed ligand libraries will be combined with ligand structure and protein descriptors to accelerate the development of new purification solutions addressing the increased challenges facing biopharma due to increased molecular diversity in the pipeline.
The Post-Doctoral Program takes the innovative research proposals of GE Life Sciences teams and places the research, development, and delivery of these inventions in the hands of our Post-Doctoral Investigators and the cross-functional teams working with them.
We are looking for someone with entrepreneurial spirit to join the leagues of innovative thinkers driving the development of world-changing technology, taking responsibility for the experimental part as well as the mechanistic modelling of downstream unit operations.

This is a temporary position of 12 months. Please apply no later than 15 January 2020.
For questions, please contact hiring manager Eva Heldin: tel. +46 (0)18 612 0391 or [email protected]


Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


Qualifications/Requirements:
Ph D with focus on modelling of preparative chromatographic separations or equivalent knowledge or experience
Experience from modelling software e.g. ChromX or CADET
Basic programming e.g. Phyton and Mathlab
Experience of performing independent research or development activities
Proven ability to plan, execute and model chromatographic experiments
Good communication skills (both written and spoken), including presentation skills
Team player and ability to work well in a multidisciplinary environment
Fluent in English and/or Swedish, both verbally and in writing
Entrepreneurial spirit



Desired Characteristics:
Experience in Quantitative Structure Property Relationship modeling including ligand structure and potentially protein structure descriptors
Experience from Design of Experiment (DoE) tools Visa mindre

Nordic Controller

The Nordic Controller is responsible for ensuring that all statutory and US GAAP requirements are met across the group of legal Nordic legal entities (Norway, Sweden, Finland and Denmark). They will provide support for the Accounting Operations teams to ensure financial statement accuracy for US GAAP and Statutory Accounting and will provide guidance to local Business teams on operational and accounting matters. Preferred location: Uppsala Sweden Essent... Visa mer
The Nordic Controller is responsible for ensuring that all statutory and US GAAP requirements are met across the group of legal Nordic legal entities (Norway, Sweden, Finland and Denmark). They will provide support for the Accounting Operations teams to ensure financial statement accuracy for US GAAP and Statutory Accounting and will provide guidance to local Business teams on operational and accounting matters.
Preferred location: Uppsala Sweden

Essential Responsibilities:
Lead a team of local accounting personnel focused on Statutory and US GAAP reporting activities for the Nordic entities.
Coordinate the Preparation of all the necessary Board of Directory meeting documents
Build strong relationships with the Finance & Operational teams and have the necessary expertise to understand and resolve technical or operational issues in the region and engage the relevant team or CoE as required. Provides Country specific expertise and language support
Regularly Review the financial analysis of balance sheet accounts prepared by our service providers to ensure US GAAP compliance, integrity of account balances/financial reporting and effectiveness of business processes
Monitor and regularly review the financial ledgers of each legal entity & ensure compliance with local laws/GAPs, tax codes, government regulations and Statutory and Tax filing requirements.
Support the Accounting Operations Finance team on the annual statutory audit with EY/ KPMG for the region including SOX Audit support
Ensure appropriate sign off of audited financial statements and appropriate Board representation
Key local contact for EY/ KPMG auditor and tax authorities
Drive closure of open audit issues (both KPMG & internal audit) and proactively work to prevent future issues / manage risk. Oversee resulting corrective action process in Accounting Operations
Monitor and review that appropriate Internal Controls are in place, in line with local statutory laws and US GAAP, and critically examine potential issues where financial risks & opportunities may be drawn out
Oversee account reconciliations, KPI’s and closing activities for the region ensuring high quality and timely delivery of financial information from Accounting Operations
Proactively lead adherence to the compliance policies
Supports business changes and transformations including acquisitions / disposals
Identify potential risks and opportunities and communicate effectively to key stakeholders
Manage the fiscal budget for the Nordic Controllership team. Monitor actuals and present information to the Controller and CFO

Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.
For more information about the position please contact Biopharma Corporate Controller Jim Schott: [email protected] +1 513 667 7028
Last day to apply is January 31st
 
Qualifications/Requirements:
Qualified Accountant with significant post qualification experience OR Bachelor’s degree in accounting, finance, or other business-related field and major progressive accounting or finance experience or equivalent knowledge or experience.
Fluent in English, written and spoken and one of the nordic languages
Proficiency in U.S. GAAP or another internationally recognized accounting framework and authoritative accounting literature
Proficiency in Swedish GAAP for entity structure consolidation and reporting
EU Work Permit is required

 
Desired Characteristics:
Integrity: accepting and adhering to high moral, ethical, and personal values in decisions, communications, actions and when dealing with others
External focus: capable of forging strong relationships with finance and non-finance leaders
Excellent verbal and written communication skills and the ability to communicate complex accounting matters clearly
Encourage teamwork & Co-operation to achieve the common aim. ”He or she is a good team player”.
Clear thinker / problem solver: successfully led projects/process improvements within operations/finance functions; able to quickly grasp new ideas
Strong analytical skills: able to clearly link financial results to operational performance drivers, generate alternatives and drive positive change
Adaptable/Flexible: being open to change in response to new information and in different or unexpected circumstances
Proficient use of financial systems Visa mindre

Vikariat processingenjör inom Kemisk Produktion Uppsala

Chemical Production Uppsala (CPU) med ca 400 anställda tillverkar kromatografimedia för rening av biologiska läkemedel. Nu har vi ett vikariat som Processingenjör, ca 9 månader, inom sektionen Process Improvements. Huvudsakliga arbetsuppgifter: I tjänsten ingår att arbeta med processförbättringar i vår tillverkning av Bioprocessmedia, delta i nyproduktprojekt tillsammans med forskningsavdelningen, supportera produktionen vid problem samt att ha processan... Visa mer
Chemical Production Uppsala (CPU) med ca 400 anställda tillverkar kromatografimedia för rening av biologiska läkemedel. Nu har vi ett vikariat som Processingenjör, ca 9 månader, inom sektionen Process Improvements.

Huvudsakliga arbetsuppgifter:
I tjänsten ingår att arbeta med processförbättringar i vår tillverkning av Bioprocessmedia, delta i nyproduktprojekt tillsammans med forskningsavdelningen, supportera produktionen vid problem samt att ha processansvar för befintliga produkter, vilket bl.a. inkluderar, trendning och styrning, kvalitetsutredningar, uppskalningar och flyttar mellan produktionsenheter.
Processansvaret innebär även ett ägande av processernas kritiska parametrar och kravställande vid investerings- och digitaliseringsprojekt.
Produktionen i Uppsala är i stark tillväxtfas och genomför flera stora investeringar, digitaliseringsprojekt och produktlanseringar.
Samarbeta med R&D, QC, QA, planering och mottagande produktionsenheter vid utveckling och mottagning av nya produkter
Stödja producerande enheter för att säkerställa EHS, kvalitet och kundleverans
Driva processvårdsprojekt, upp- och nedskalningar samt flytt av processer
Ansvar för trendning av kvalitetsutfall och genomförande av grundorsaksanalyser inkl. följa CAPA-rutiner
Ansvar för genomförande av förändringar i befintlig produktion enligt Change Control-rutiner
Driva och delta i förbättringsarbete och problemlösning
Upprätta och uppdatera tillverkningsdokument
Genomföra Process Safety riskanalyser

Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.
 
Kvalifikationer:
Civilingenjör eller motsvarande med inriktning mot kemi/kemiteknik/bioteknik eller liknande.
Intresse för tillverkningsprocesser
Goda kunskaper i svenska och engelska.
God kommunikationsförmåga
Förmåga att kunna driva flera aktiviteter samtidigt
Kunna ta initiativ och fatta beslut
Förmåga att jobba i grupp och självständigt
Kunna se konsekvenserna av beslut eller aktivitet innan den genomförs
God problemlösningsförmåga


Vi ser gärna att du:
Erfarenhet av processindustri
Erfarenhet av problemlösning och 6Sigma Visa mindre

UX/IX Designer

We are looking for a UX/Ix Designer to join the System Engineering & UX section, Downstream Systems R&D organization in Uppsala. The Downstream System and Software team develops systems (instruments and software) for liquid chromatography used for protein purification, as well as other devices and software to support the customer workflows in the Bioprocess area. Within the departments, located in Uppsala & Umeå, we have many competences: software, mechani... Visa mer
We are looking for a UX/Ix Designer to join the System Engineering & UX section, Downstream Systems R&D organization in Uppsala.
The Downstream System and Software team develops systems (instruments and software) for liquid chromatography used for protein purification, as well as other devices and software to support the customer workflows in the Bioprocess area. Within the departments, located in Uppsala & Umeå, we have many competences: software, mechanics, electronics & applications engineering. The development is driven in cross-functional, global project teams where we create products for the Life Sciences industry.

Essential Responsibilities:
As a UX/Ix designer, you will contribute to the understanding of our customers and the users of our products. You will work in close collaboration with developers and system engineers to create innovative and desirable solutions to our customers challenges. In this role you will execute on multiple small to medium-sized projects as an individual contributor with a focus on UX and interaction design.
The UX/Ix designer will work within global, cross-functional product development teams to optimize software interfaces by applying deep domain expertise in human cognitive and physical capabilities, and insights about user needs.
Duties include (but are not limited to):
As part of a team, plan and deliver the team's commitments
Work closely with the front-end developers, application specialists, PO’s and system architects
Prototype and design graphical design elements and user interfaces
Plan and facilitate end user testing with low and high-fidelity prototypes
Propose design and product solutions based on user needs
Create interaction design specifications for development teams and continuously test the user experience
Create the overall interaction scheme and layout in relation to the product concept
Present, both orally and in writing, results and conclusions from work performed
Stay up to date on current trends and techniques in the IxD field
Continuously improve our ways of working

Representative deliverables include user personas, graphical design elements, mock-ups, prototypes, wireframes, task analyses, usability test reports, use cases, flow charts and storyboards.
Please apply no later than 12 January 2020.
For questions, please contact hiring manager Johan Nyberg: tel. +46 (0)76 720 99 45 or [email protected]


Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.
 
Qualifications/Requirements:
MSc or BSc within the UX field or equivalent knowledge or experience
Strong experience as a UX designer or IxD within a product development environment
Hands-on experience with a combination of the following: low and high-fidelity prototype creation and testing, rapid iterative testing, survey design, lab-based usability testing, remote usability testing
Prototyping skills, mock-ups, wireframes and interactive prototypes
Experience designing desktop, web and mobile applications
Ability to facilitate workshops to gain a group understanding of research data and leverage data to derive actionable insights
Knowledge and experience of project models and agile scrum methodologies
Excellent communication and presentation skills (both written and spoken)
Structured and organized team player with good interpersonal skills
Takes initiative to learn new tools and techniques and integrates new methods to drive improved outcomes
Swedish and English as working languages



Desired Characteristics:
Experience in integrating digital and physical products
Experience in graphical design
Great interest in technology
Experience in developing design systems
Experience working in multidisciplinary environments
Experience working on large, complex, global projects
An understanding of key principles of design thinking, what it is and why it is important.

The work is conducted in close cooperation with specialists from different parts of R&D such as system engineering, software development and application specialists. It is desirable for applicants to have interest and insight in these areas. Visa mindre

Processoperatör

Vi söker nu en processoperatör till sektionen Advanced Manufacturing Engineering & Pilot Plant, inom Kemisk produktion i Uppsala. Vi är idag en grupp på 2 operatörer, 1 Teamleader och 7 ingenjörer som tillverkar och utvärderar framtida tillverkningsprocesser för kromatografimedia och cellseparationsprodukter till läkemedelstillverkande kunder. Tjänsten är en tillsvidareanställning och tillsättes snarast. Arbetet sker på vanlig dagtid och vi tillämpar flex ... Visa mer
Vi söker nu en processoperatör till sektionen Advanced Manufacturing Engineering & Pilot Plant, inom Kemisk produktion i Uppsala. Vi är idag en grupp på 2 operatörer, 1 Teamleader och 7 ingenjörer som tillverkar och utvärderar framtida tillverkningsprocesser för kromatografimedia och cellseparationsprodukter till läkemedelstillverkande kunder.
Tjänsten är en tillsvidareanställning och tillsättes snarast. Arbetet sker på vanlig dagtid och vi tillämpar flex vilket underlättar balansakten mellan privat- och arbetsliv.




Huvudsakliga arbetsuppgifter:
Operatörsarbetet präglas av variation och en möjlighet till att påverka den dagliga verksamheten, där processerna är i fokus men det självständiga förbättringsarbetet fortgår under reaktionstiderna. I arbetet ingår även att delta vid utveckling och utvärdering av olika moderna tekniker för tillverkning.


Som operatör kommer du i första hand att arbeta med:
• Tillverkning av separationsprodukter
• Styrning av process och utrustning via styrsystem
• Provuttag och enklare analyser i processlab
• Koordinering med andra sektioner som uppvägning, underhåll, kvalitetskontroll och förråd
• Kalibrera och underhålla utrustning
• Medverka i förbättringsarbetet av processer och utrustning, genom t.ex. Lean Management
• Medverka i utbytesprojekt där gammal utrustning ersätts med modern
• Delta i pilotverksamheten vid utvärdering och utveckling av framtidens separationsmediaproduktion
• Utfärda arbetstillstånd till entreprenörer


Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


Kvalifikationer:
• Gymnasieutbildning inom kemi eller med annan teknisk inriktning
• Erfarenhet av kemikaliehantering och/eller brandfarliga varor
• Tekniskt intresse och erfarenhet gällande förebyggande och avhjälpande underhåll
• Goda kunskaper i svenska och engelska


Vi ser gärna att du:
• Har erfarenhet inom biotech- eller läkemedelsindustrin
• Har ledaregenskaper
• Har erfarenhet av att arbeta med styrsystem
• Har erfarenhet/kännedom av systematiskt underhållsarbete av processanläggningar
• Har erfarenhet av förbättringsarbete genom t.ex. Lean Management
• Är datorvan och trygg i IT-miljö (generell förståelse för Excel, Outlook och ärendehanteringssystem)


Vi söker dig som är engagerad och gärna arbetar i lag. Du är nyfiken, lättlärd och inspireras av utmaningar! Som person är du säkerhetsmedveten, noggrann och mån om att alltid leverera bästa kvalitet till kunden Visa mindre

Electrical Engineer

We are looking for a self-driven and accountable Electrical Engineer to the BioProcess Systems department. You will join a team that develops the next generation of protein separation systems that are used for development and manufacturing of medicines. You will belong to a team of 20 highly skilled electrical and mechanical engineers. Essential Responsibilities: Development of electronics for BioProcess systems with pumps, sensors, motors, robotics, et... Visa mer
We are looking for a self-driven and accountable Electrical Engineer to the BioProcess Systems department.
You will join a team that develops the next generation of protein separation systems that are used for development and manufacturing of medicines. You will belong to a team of 20 highly skilled electrical and mechanical engineers.

Essential Responsibilities:
Development of electronics for BioProcess systems with pumps, sensors, motors, robotics, etc.
You will be developing PCA boards, sensors, cables, communciation interfaces, etc for our systems with focus on product performance, quality and production cost.
We develop systems mainly according to EN61010 and EN60204

Please apply no later than 31 January 2020.
For questions, please contact Hiring Manager Thomas Arctaedius, tel. +46 (0)73 045 51 04 or [email protected]
Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.
 
Qualifications/Requirements:
Significant experience within electrical engineering
Bachelor’s degree in Electrical Engineering or equivalent knowledge or experience
Structured and organized team player with good interpersonal skills
Good skills in Swedish and English, both oral and written


Desired Characteristics:
Experience from designing electronics for integrated systems Visa mindre

Automationsingenjör - DCS

Vill du vara med och ta det digitala språnget i vår världsledande produktionsanläggning i Uppsala? Nu utökar vi vårt professionella automationsteam! Vi söker nya medarbetare som är med och tar vår världsledande produktion in i nästa era. Vi inom System Support & Development tar ansvar för drift, support och utveckling av det digitala landskapet inom den kemiska produktionen i Uppsala. Just nu befinner vi oss i en spännande utrullning av vår nya digitala ... Visa mer
Vill du vara med och ta det digitala språnget i vår världsledande produktionsanläggning i Uppsala? Nu utökar vi vårt professionella automationsteam!
Vi söker nya medarbetare som är med och tar vår världsledande produktion in i nästa era. Vi inom System Support & Development tar ansvar för drift, support och utveckling av det digitala landskapet inom den kemiska produktionen i Uppsala.
Just nu befinner vi oss i en spännande utrullning av vår nya digitala plattform som kommer befästa vår världsledande position. Vårt mål ett landskap där vi till fullo utnyttjar potentialen i vår digitala ryggrad bestående våra DCS system (ABB 800xA), eBR (Werum PAS-X), ERP (Oracle) samt kommande SPC och LIMS.
Till denna resa stärker vi vårat team med tre nya roller så teamet kommer att bestå av 18 engagerade specialister.


Huvudsakliga arbetsuppgifter:
Som automationsingenjör – (DCS) har du en ledande roll i att utveckla våra automationssytem (ABB 800xA) och tillhörande infrastruktur.
Arbetsuppgifterna består bland annat av:
Nyckelroll i projekt för att säkra sitens automationsstandard
Leda och operativt utföra aktiviteter kopplade till vår automationsstrategi
Utveckla automationsområdet (DCS) för bättre funktionalitet, operatörsupplevelse och output
Supportera verksamheten och utföra avhjälpande åtgärder
Rollen erbjuder stora möjligheter att vara del av den digitala utvecklingen av produktionen. Du kommer både att leda aktiviteter men också vara specialisten som säkerställer automationsfunktionalitet i anläggningarna och i projekt.

För närvarande pågår integrering av våra ABB 800xA system med vår MES plattform (Werum PAS-X).
Du är självklart lösningsorienterad och ser vikten av att arbeta förebyggande för att skapa en driftsäker anläggning.


Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.
 
Kvalifikationer:
Examen från högskola eller universitet med relevant inriktning, eller erfarenhet från arbete i liknande roll, eller mångårig erfarenhet från produktion där automationssystem är ett dagligt verktyg
Erfarenhet från processindustri
Mycket goda kunskaper om automationssystem, med fördel ABB 800xA
Det är naturligt för dig att kommunicera på Svenska och Engelska
Goda kunskaper i planering och genomförande
Ett brinnande intresse för digitalisering



Önskvärda egenskaper:
Kunskap om systemintegration
Erfarenhet av supportverksamhet och aktiv systemförvaltning
Brett kontaktnät i branchen Visa mindre

Regulatory Support Manager

The Regulatory Support Manager will have responsibility 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. Essential Responsibilities: As a member of the Customer Regulatory Support team, you will add value to bioprocess products and demonstrate a commitment to customer Build and maintain knowle... Visa mer
The Regulatory Support Manager will have responsibility 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.


Essential Responsibilities:
As a member of the Customer Regulatory Support team, you will add value to bioprocess products and demonstrate a commitment to customer
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
Lead cross-functional activities when required
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, HWPD, CCN, statements, certificates and other regulatory related documentation for new and existing products
Use existing web based system and expand regulatory supporting information provided on the web



Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


Qualifications/Requirements:
Bachelor of Science degree in Chemistry, Pharmacy or other related field or equivalent knowledge or experience
Strong experience in quality, product management or a related field
Understanding of GMP and knowledge of regulatory requirements in the bioprocess industry
Organized, accurate, target oriented, quality minded and customer oriented
Strong written and verbal communication skills
Flexible and service-minded with the ability to be collaborative
Strong ability to work independently, drive



Desired Characteristics:
Significant experience with biopharmaceutical or cell and gene therapy process development and quality assurance
Expertise in the medical regulatory field
Experience in GE Healthcare product development or production.
Experience leading cross-functional activities
Strong computer skills with prior experience in systems, including Microsoft Office products, Magic, Oracle and Lotus Notes

For more information contact recruiting manager Ondina Åsberg +46 186120535 or [email protected]


Welcome with your application! Visa mindre

Laboratoriespecialist

Vi söker en laboratoriespecialist till Quality Control i Uppsala. Avdelningen Quality Control (QC) arbetar med att kvalitetskontrollera produkter från vår produktion i Uppsala. Huvudsakliga arbetsuppgifter: I rollen som laboratoriespecialist arbetar du främst med att analysera produkter enligt gällande instruktioner och rutiner samt bedöma analysstatus. Du arbetar också med att starta och driva undersökningar vid avvikande analysresultat, utföra kalibrer... Visa mer
Vi söker en laboratoriespecialist till Quality Control i Uppsala.
Avdelningen Quality Control (QC) arbetar med att kvalitetskontrollera produkter från vår produktion i Uppsala.


Huvudsakliga arbetsuppgifter:
I rollen som laboratoriespecialist arbetar du främst med att analysera produkter enligt gällande instruktioner och rutiner samt bedöma analysstatus. Du arbetar också med att starta och driva undersökningar vid avvikande analysresultat, utföra kalibreringar och underhåll av analysinstrument samt uppdatera och godkänna arbetsinstruktioner.


Utföra analyser enligt gällande instruktioner
Avrapportera, kontrollgranska och utföra analysacceptans på produkter och uppdragsanalyser
Starta och driva undersökningar vid avvikande analysresultat och andra avvikelser
Utföra kontroller, kalibreringar och underhåll av analysinstrument
Uppdatera och godkänna arbetsinstruktioner (kontrollmetoder, standardmetoder och kalibreringsmetoder)



Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.


Kvalifikationer:
Lämplig bakgrund är högskoleingenjör/gymnasieingenjör inom Kemi/Analytisk kemi/Biokemi eller liknande.


Vi söker dig som är:
noggrann och strukturerad
flexibel
bra på att samarbeta
positiv samt uppmuntrar och inspirerar andra

Vi vill också att du har förmåga att utföra flera olika arbetsuppgifter parallellt, gillar att arbeta i förändring och att driva förändringsarbete.


Önskvärda egenskaper:
Tidigare erfarenhet av laborativt kvalitetsarbete inom QC-verksamhet, gärna inom kromatografi
Datorvana MS office
Erfarenhet från arbete med Lean
Svenska och engelska i både tal och skrift Visa mindre

DevOps Software Engineer

Dina huvuduppgifter som DevOps Software Engineer på GE Healthcare i Uppsala är att designa, implementera, underhålla och optimera den miljö som används för mjukvaruutveckling, byggnad och distribution. Utvecklingsmiljön är Windows-baserad. Du kommer att ingå i ett team som är huvudnavet för all programutveckling som sker på vår FoU-avdelning. Det betyder att teamarbete är viktigt eftersom utmaningar kommer från alla håll. Du och teamet hjälper varandra at... Visa mer
Dina huvuduppgifter som DevOps Software Engineer på GE Healthcare i Uppsala är att designa, implementera, underhålla och optimera den miljö som används för mjukvaruutveckling, byggnad och distribution. Utvecklingsmiljön är Windows-baserad.
Du kommer att ingå i ett team som är huvudnavet för all programutveckling som sker på vår FoU-avdelning. Det betyder att teamarbete är viktigt eftersom utmaningar kommer från alla håll. Du och teamet hjälper varandra att underhålla och utveckla vår miljö så att utvecklarteamen kan bygga/testa/släppa ny programvara på ett effektivt sätt.


Huvudsakliga arbetsuppgifter:
Vår avdelning utvecklar programvara som används av universitet och läkemedelsföretag för upptäckt och utveckling av biologiska läkemedel för att bekämpa sjukdomar som cancer och diabetes.
Eftersom vår övergång till molnbaserade lösningar pågår kommer du att spela en viktig roll i denna övergång och ha möjlighet att påverka inriktning och slutresultat.


Arbetsuppgifter kommer i huvudsak bestå av:
Drift, support och optimering av CI-miljön
Cloud infrastruktur: automatisering, konfiguration och övervakning
CI/CD: som en del av teamet utveckla och underhålla automatiska byggen, test och driftsättningar

Sista ansökningsdag: 10 januari 2020.
För frågor, kontakta rekryterande chef Johan Tschöp: tel. +46 (0)18 612 00 69 eller [email protected]


Vänligen notera att denna roll kommer att ligga inom ramen för den föreslagna övergången av GE Biopharma till Danaher och kommer att övergå till Danaher när denna transaktion slutförs.
Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.
 
Kvalifikationer:
Utmärkta kunskaper i svenska och engelska, både tal ock skrift
Examen i datavetenskap eller liknande
Några års erfarenhet från professionell programvaruutveckling (C # .NET och GIT)
Erfarenhet från DevOps-position
Erfarenhet och kunskap i att arbeta i en smidig utvecklingsmiljö
Arbetstillstånd för EU



Önskvärda egenskaper:
Erfarenhet från att arbeta med Azure DevOps.
Intresse och erfarenhet från att utveckla och underhålla automatiska bygg- och smoketester.
Erfarenhet från automatiserad GUI-testning.
Att få saker att fungera smidigt, men samtidigt inse att verkligheten är allt annat än smidig hela tiden.
Att vara serviceinriktad och lösningsorienterad kommer definitivt att hjälpa till att utmärka sig i denna roll Visa mindre

Mekanikingenjör

Arbete som Mekanikingenjör sker inom Kemisk Tillverkning i Uppsala, avdelning QC på sektion QC Material Supply. Sektionen består av 17 personer varav 2 personer arbetar på mekaniklabbet (där denna tjänst ingår). Sektionen har två huvudsakliga syften: att kvalitetskontrollera och fatta beslut om status för inköpt material (kemiska råvaror och komponenter) att ansvara för sajtens råvaruförråd som hanterar in- och utleveranser av inköpt material Huvudsakli... Visa mer
Arbete som Mekanikingenjör sker inom Kemisk Tillverkning i Uppsala, avdelning QC på sektion QC Material Supply. Sektionen består av 17 personer varav 2 personer arbetar på mekaniklabbet (där denna tjänst ingår). Sektionen har två huvudsakliga syften:
att kvalitetskontrollera och fatta beslut om status för inköpt material (kemiska råvaror och komponenter)
att ansvara för sajtens råvaruförråd som hanterar in- och utleveranser av inköpt material



Huvudsakliga arbetsuppgifter:
Som Mekanikingenjör arbetar du främst med ankomstkontroll av mekanikmaterial och fattar/verkställer status på dessa. I tjänsten ingår även att arbeta med avvikelsehantering, grundorsaksutredningar och ständiga förbättringar m a p kvalitet, förenkling och EHS. Som Mekanikingenjör fungerar du även som back up till sektionens Product Quality Engineer för inköpt mekanikmaterial. I rollen ingår även att fungera som resurs inom QC-avdelningen inom områden där den egna kompetensen är god.
Ankomstkontroll av inköpt mekanikmaterial, kontrollgranskning av kollegors mätresultat och fatta beslut/verkställa beslut om status
Självständigt driva arbete kring avvikelsehantering, genomföra grundorsaksanalyser och implementera åtgärder
Arbeta systematiskt med förbättringsarbete inom kvalitet, förenkling och EHS (arbetsmiljö)
Fungera som ersättare för sektionens Product Quality Engineer (PQE) för mekanikmaterial vid dennes frånvaro



Kvalifikationer:
Högskoleexamen eller motsvarande inom relevant teknikområde (mekanik, maskin) eller annan lämplig utbildning kombinerad med erfarenhet från bioteknisk eller läkemedelsindustri
Erfarenhet av kvalitetskontroll och beslutsfattande av status m a p komponenter inom bioteknisk/läkemedelsindustri
Erfarenhet av mekanisk uppmätning och olika mättekniker
Erfarenhet av att självständigt driva arbete med avvikelsehantering och grundorsaksanalyser samt implementering av korrigerande åtgärder
Erfarenhet av systematiskt förbättringsarbete, t ex gnm LEAN
God förmåga att uttrycka sig i tal och skrift på svenska och engelska, men behärskar också teknisk terminologi på båda språken
Då mekaniklabbet endast består av två personer lägger vi stor vikt vid personlig lämplighet utöver de rena kvalifikationskraven



Önskvärda egenskaper:
God samarbetsförmåga
Resultat- och målinriktad
Ansvarstagande
Noggrann
Initiativrik
God problemlösningsförmåga
Orädd att arbeta i olika datasystem
Intresse för att jobba med mekanik & instrument Visa mindre

Sektionschef inom storskalig kemiproduktion

Vi söker dig som vill leda en sektion inom storskalig kemiproduktion med ansvar för tillverkning av kromatografimedia. Som sektionschef har du ett ansvar för produktion, personal och produktkvalitet. Huvudsakliga arbetsuppgifter: Det är ett omväxlande arbete där du förutom att ha personalansvar för sektionens 20 medarbetare även arbetar med förbättringsarbete, processvårdsaktiviteter, initiera och driva underhållsarbete samt ta emot och skala upp nya pro... Visa mer
Vi söker dig som vill leda en sektion inom storskalig kemiproduktion med ansvar för tillverkning av kromatografimedia. Som sektionschef har du ett ansvar för produktion, personal och produktkvalitet.


Huvudsakliga arbetsuppgifter:
Det är ett omväxlande arbete där du förutom att ha personalansvar för sektionens 20 medarbetare även arbetar med förbättringsarbete, processvårdsaktiviteter, initiera och driva underhållsarbete samt ta emot och skala upp nya produkter. Du förväntas ha ett nära samarbete med andra funktioner och ingår även i avdelningens ledningsgrupp.
Sektionen tillhör avdelningen Produktion 1 som är en av avdelningarna inom Chemical Production Uppsala (CPU) som består av totalt ca 400 anställda.
Leda en sektion inom storskalig kemiproduktion med ansvar för tillverkning av Sephadex basmatriser och slutprodukt.
Förutom reguljär tillverkning ingår i ansvaret att initiera processvårdsaktiviteter, driva change-control ärenden, initiera och driva underhållsarbete, ansvara för ständiga förbättringar, ta emot och skala upp nya produkter, ekonomisk uppföljning samt att initiera och driva business case för investeringar
Som sektionschef jobbar du i nära samarbete med planeringsfunktionen, QC, QA, produktchefer och konstruktionsansvariga. Vidare har du mycket kontakter med underhållsavdelningen, projekt-avdelningen och produktionens driftavdelningar
I ansvaret ingår att förevisa verksamheten för kunder samt besvara frågor i samband med revisioner
Du ingår i avdelningens ledningsgrupp och du har arbetsmiljö-, personal- och budgetansvar för sektionen.



Vänligen notera att denna roll kommer att ligga inom ramen för den föreslagna övergången av GE Biopharma till Danaher och kommer att övergå till Danaher när denna transaktion slutförs.
Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction.
 
Kvalifikationer:
Högskolekompetens (kemiteknik eller motsvarande) med lång arbetslivserfarenhet inom området
Erfarenhet av att leda och utveckla team
Goda ledaregenskaper såsom beslutsamhet, drivande och förmåga att entusiasmera
Utmärkt skriftlig och verbal kommunikationsförmåga på alla nivåer
Erfarenhet av ekonomisk uppföljning
Förmåga att bedriva ständigt förbättringsarbete
Ledarerfarenhet från produktion/tillverkning
Erfarenhet av projektledning och LEAN
Kunskap om kemiska processer och utrustning



För mer information rörande tjänsten, vänligen kontakta Jonas Kärvin (Rekryterande Chef) Visa mindre