Lediga jobb som Utvecklingschef i Uppsala

Job description
Are you ready to make an impact in a global, cutting-edge environment? Pharmetheus, a leader in pharmacometrics consultancy, is expanding!
We’re at the forefront of supporting drug development through quantitative analysis and are now building our product development team. Join our dynamic System Development team as a Product Owner, with opportunities to grow into a hybrid Product Owner/Business Analyst role.
About the role
As a Product Owner at Pharmetheus, you'll be at the heart of transforming business needs into actionable product solutions. Your role will involve driving product success by prioritizing product backlogs, managing change requests, and collaborating closely with our QA team to deliver top-notch product documentation.
You won't just be managing a backlog; you'll be the commercial-technical glue of the company—equipping our Sales and Marketing experts with the product insights they need to succeed. You'll also be the bridge between key stakeholders, identifying risks and unlocking new opportunities to fuel our innovation. If you're ready to make a tangible impact in the fast-paced world of drug development, this is your chance to shine!


In this recruitment, Pharmetheus AB is partnering with Randstad. Selection is ongoing, and we encourage you to submit your application as soon as possible. If you have any questions regarding the role or the process, please contact Recruitment Consultant Erik Perborn at [email protected]

Responsibilities
Analyze pharma clients user and business needs and transform them into value-driven product roadmaps and requirements
Prioritize product backlogs and manage change requests
Manage stakeholder relationships, from technical teams, internal and external, to clients, through sales and marketing, and identify risks and opportunities
Collaborate with our QA team, maintain product documentation and translate it to high-level sales enablement material
Contribute to commercial readiness


Qualifications
To fit in this position you have a Bachelor’s degree in Business, Operations Management, or you have worked in a similar role before which is considered equivalent along with several years of experience in Business Analysis or Product Ownership. Your background should include expertise in SaaS and software development, and you have to be fluent in English.
If you bring additional experience from the pharma industry, regulatory environments, or academia, you'll stand out even more. Familiarity with the Atlassian suite (Jira, Confluence) and a certification as a Scrum Product Owner, along with a solid grasp of agile practices, will give you an edge and make you an ideal candidate for our dynamic team.
Required Skills
Bachelor’s degree in Business, Operations Management, or similar
3+ years of experience in Product Ownership, Product Management, with emphasis on Business Analysis, product launches, and GTM cycles
Experience in SaaS and software development
Strategic communicator with commercial insight
Fluent in English

Preferred Skills
Pharma industry, regulatory, or academic experience
Familiarity with Atlassian suite (Jira, Confluence)
Certified Scrum Product Owner and agile practices knowledge


About the company

Randstad
På Randstad vet vi att alla människor har en plats på arbetsmarknaden. Med verksamhet över hela landet och inom alla kompetensområden hjälper vi människor att hitta ett jobb som känns bra, och där de får möjlighet att växa, utvecklas och uppnå sin fulla potential. Med närmare 600 000 anställda i 38 länder är Randstad världsledande inom HR-tjänster, med målsättningen att bli världens främsta och mest uppskattade partner på arbetsmarknaden. Genom att kombinera vår passion för människor med kraften i dagens teknologi hjälper vi människor och företag att uppnå deras fulla potential. Vi kallar det Human Forward. Visa mindre

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

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

Interviews and selections will be conducted continuously, and the position may be filled before the application deadline of May 16th.
We look forward to hearing from you and discussing how you can contribute to our team.
Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Visa mindre

Flygvapnets Utvecklingsenhet Luftstrid (UTV Luft) rekryterar civil chef till Studieavdelningen.
Vill du ha möjligheten att vara med och utveckla Flygvapnets förmågor för framtiden? Studieavdelningen genomför studier inom ramen för Flygvapnets långsiktiga utveckling, genomför experimentverksamhet och bedriver erfarenhetsanalys. Som chef kommer du att spela en nyckelroll i utvecklingen av Flygvapnets framtida förmågor, du kommer att leda ett team bestående av kvalificerad civil och militär personal.

 

Kort om enheten UTV LUFT:

För att vidmakthålla Flygvapnets operativa förmåga kräver flygstridskrafternas insatsförband kontinuerlig utveckling både på kort och lång sikt.

UTV LUFT tillhör Luftstridsskolan (LSS) och genomför Flygvapnets förmågeutveckling vad avser teknik, taktik och metod för samtliga Flygvapnets förband och funktioner.  Verksamheten spänner över såväl materielutveckling som konceptutveckling till förmågeintroduktion vid insatsförbanden.


Sökande avdelning:

LSS UTV LUFT, Studieavdelningen

Studieavdelningen är en del av UTV LUFT. Uppgifterna inom studieavdelningen omfattar konceptutveckling, studier samt övrig långsiktig förmågeutveckling med bl.a. stöd till försvarsmaktens inriktnings- och planeringsprocess, Flygvapnets experimentkontor och erfarenhetsanalys.


Arbetsuppgifter:

Som chef för Studieavdelningen är du underställd chefen för UTV Luft och kommer att leda en grupp om ca 5-10 medarbetare bestående av både civil och militär fast placerad personal samt konsulter.


Ansvarsområden:


• Leda och utveckla avdelningens verksamhet
• Budget- och personalansvar för avdelningen

 

Krav:


• Du har en akademisk examen eller motsvarande på avancerad nivå
• Mycket god förmåga i tal och skrift på svenska och engelska.
• Mycket god analytisk förmåga.
• Erfarenhet av chefskap
• B-körkort


Önskvärda kvalifikationer:


• God förmåga till självständigt arbete, god förmåga att leda verksamhet och att leverera efterfrågade resultat i tid.
• aktuell erfarenhet av studiearbete och/eller operationsanalys
• projektledarutbildning
• erfarenhet från militär utvecklingsverksamhet
• erfarenhet av Concept Development & Evaluation (CD&E)

 

Personliga egenskaper:


• Du har en utvecklad samarbetsförmåga och social förmåga såväl internt som mot externa kontakter.
• God förmåga att anpassa dig till nya roller och omständigheter och att du har ett tvärvetenskapligt synsätt.
• Du har förmågan att bygga och upprätthålla nätverk.
• Du är prestigelös och har förmåga att lära av erfarenheter
• Du kan arbeta och leverera goda resultat i olika tempon
• Goda ledarskaps- och kommunikationsförmågor

Stor vikt kommer att läggas vid personlig lämplighet.

 

Upplysningar om tjänsten kan lämnas av:
Övlt Mattias Hansson, chef UTV Luft, 070-970 67 61

För Information om rekryteringsprocessen kontakta:
HR-generalist Linda Göthberg, 072-388 12 13



Fackliga företrädare:

OFR/O Ärna Tim Björklund, tfn 070-649 65 59
OFR/S & Försvarsförbundet Helena Lemnell tfn 070-836 10 28
SEKO Åsa Karlsson nås via vx 018-19 60 00
SACO nås via vx 018-19 60 00

 

Övrigt:


• Civil befattning
• Anställningsform: Tillsvidareanställning, provanställning om 6 månader tillämpas
• Arbetsort: Uppsala
• Beräknat startdatum/tillträde: Efter överenskommelse, dock tidigast 2025-08-25.
• Tjänsten är placerad i säkerhetsklass varvid säkerhetsprövning kommer att genomföras.

 


Välkommen med din ansökan senast 2025-05-05.

Din ansökan skall innehålla CV samt ett ansökningsbrev. I ansökningsbrevet vill vi att du motiverar varför du är lämpad för denna befattning.

Ansökningar till denna befattning kommer endast tas emot via Försvarsmaktens webbplats.
--------------------------------------------------------
Information om Försvarsmakten och det rekryterande förbandet:

Luftstridsskolan är flygvapnets gemensamma kompetenscentrum för utveckling och utbildning. Luftstridsskolan har fyra flygvapengemensamma skolor och utbildar bland annat framtida piloter inom Försvarsmakten. Luftstridsskolan har verksamhet på sju orter spridda över hela landet och har sitt huvudsäte i Uppsala.

Luftstridsskolan strävar ständigt efter att utveckla hur vi löser ställda uppgifter och vi är alltid beredda att klara nya utmaningar.

I Försvarsmakten finns en stark värdegrund som bygger på öppenhet, resultat och ansvar. Professionell utveckling och personlig hälsa värdesätts och uppmuntras. Det finns goda förutsättningar för intern karriärrörlighet, friskvård samt bra balans mellan arbete och privatliv.

En anställning hos oss innebär placering i säkerhetsklass. Vanligtvis krävs svenskt medborgarskap.
Säkerhetsprövning med registerkontroll kommer att genomföras före anställning enligt 3 kap i säkerhetsskyddslagen. Med anställning följer en skyldighet att krigsplaceras. I anställningen ingår även en skyldighet att tjänstgöra utomlands. Innebörden av detta varierar beroende på typ av befattning.

Till ansökan om anställning ska CV och personligt brev bifogas. Om du går vidare i anställningsprocessen ska alltid vidimerade kopior av betyg och intyg uppvisas.

Samtal från externa rekryteringsföretag och säljare undanbedes. Visa mindre

Är du en driven ledare med erfarenhet från entreprenörskap, akademi eller näringsliv? Har du erfarenhet av att driva ett innovativt företag, affärsutveckling, leda strategiska initiativ, eller kanske forskning och utveckling?
Oavsett bakgrund kan du vara rätt person för rollen som Verksamhetsledare på Life science – ett nav i regionens innovationsekosystem.
Om rollen
Vi söker dig som kan bygga broar mellan olika sektorer, initiera och driva strategiska samarbeten samt skapa konkreta resultat för en hållbar och kunskapsbaserad tillväxt. Här får du möjligheten att använda din erfarenhet i en roll som påverkar framtiden för life science och angränsande discipliner.
Som Verksamhetsledare på Life science leder du ett team på sex projektledare och ansvarar för att initiera och driva projekt som skapar värde och tillväxt inom områden som attraktionskraft, kompetensförsörjning, innovativt företagande, testbäddar och infrastruktur. Hur vi når dit har du stor möjlighet att påverka.
I praktiken kommer du att samverka med företrädare för näringsliv, akademi, myndigheter, regionala aktörer och andra intressenter. Du ser till att såväl projekt som strategier förankras och följs. Förutom personalansvar ingår budgetansvar, inklusive ansvar för finansiering av verksamheten med externa medel. En arbetsdag kan innehålla arbete med strategiformuleringar, skriva projektansökan och att bjuda in tjänsteleverantörer och offentliga aktörer till samtal om framtida möjligheter och utmaningar. Kanske får du klippa ut några namnlappar också.
Du verkar i nära samarbete med övriga kollegor på STUNS. Du är en del av stiftelsens ledning och rapporterar till vd.
Din profilFör att lyckas i rollen behöver du ha en passion för att göra skillnad och förmågan att verka genom andra som en katalysator för förändring och utveckling. Du har kanske erfarenhet av och förståelse för industriellt utvecklingsarbete, affärsutveckling, projektledning, forskningsfinansiering och samverkan inom life science eller angränsande områden.
Vidare krävs att du har en stark nyfikenhet och förmåga att hålla dig uppdaterad om omvärldens utveckling för att kunna hantera och förstå olika intressenters mål och behov. Du ska kunna navigera mellan akademi, näringsliv och offentliga aktörer och omvandla dessa perspektiv till konkreta åtgärder som främjar framgångsrika samarbeten och hållbar tillväxt.
Erfarenhet och förmågor: Gedigen erfarenhet från life science och/eller angränsande discipliner, exempelvis inom forskning och affärsutveckling eller projektledning.
Erfarenhet av att leda och skapa engagemang och samsyn inom och mellan team, samt att stötta och utveckla teamet för att uppnå gemensamma mål.
Förmågan att lyssna, analysera och förstå samspelet mellan akademi, industri och samhälle, och vad som krävs både på kort och lång sikt för att främja utveckling och tillväxt.
Förmåga att skapa förtroende, att bygga nätverk och etablera långsiktiga samarbeten.
Erfarenhet av att arbeta med extern finansiering genom hela processen.
Goda kunskaper i svenska och engelska.
Erfarenhet av att leda komplexa samverkansprojekt.
Ansökan
Är du är rätt person för jobbet, skicka in en ansökan! Känner du dig osäker på om du uppfyller kraven slå en signal så diskuterar vi! Vi är motiverade att hitta en person med ambition och vilja att bidra.
I den här rekryteringen har STUNS valt att samarbeta med SallyQ och vi hänvisar alla dina frågor och funderingar till Sandra Bydell Sveder, Partner & Senior Rekryteringskonsult och du kan nå henne på 076-319 96 88 eller [email protected]. Vi tar emot ansökningar fram till 4 mars 2025.
Om STUNS
STUNS (Stiftelsen för samverkan mellan universiteten i Uppsala, näringsliv och samhälle) är en samverkansplattform som stärker innovationskraften och bidrar till hållbar tillväxt i Uppsala genom samarbete mellan akademi, näringsliv och offentlig sektor. STUNS stiftare är Länsstyrelsen i Uppsala län, Uppsala universitet, SLU, Region Uppsala, Uppsala kommun och Stockholms Handelskammare i Uppsala län.
Genom att förbättra förutsättningarna för långsiktigt värdeskapande innovation och företagande verkar STUNS för full kraft tillsammans. Organisationen har idag drygt 20 medarbetare samt studentmedarbetare. Visa mindre

Overview
Biotage has a world class Research & Development Function, which is located across several different sites, globally. Each R&D site is led by a Research & Development Site Leader, who report to the Chief Scientific Officer. Research & Development Site Leaders make sure that Biotage keeps up to date with competitors and market trends. They aim to provide people with better products while boosting a company’s profits.
In this role, you’ll lead a company’s R&D team and product improvement efforts, from a specific site. From developing workflows, that include developing applications notes to creating new equipment items for consumers, you will be involved in finding ways to enhance current products and developing new ones that match forecasted trends.
It can be a high-pressure job with many targets to hit, where you’ll need a strong knowledge of both science, business and leadership. But as an R&D manager you will be involved with exciting projects and work in all kinds of environments with various people.
You will work closely with the Chief Scientific Officer to establish a working plan to direct R&D resource in appropriate ways to allow the delivery of new products, improvements and corrective measures so that Company objectives are satisfied.
Role and responsibilities:
Daily tasks will vary but could involve:
Ensuring Health and Safety policies and protocols are clearly defined, fit for purpose and implemented effectively
Liaising with Product Management, Marketing, HR, Finance, Production, Operations, Intellectual Property, Product Care, Commercial functions to ensure that all project stakeholders are held accountable and notified of project status
Reporting into the Executive Leadership Team (when required) to give updates on R&D progress
Using creative skills and research knowledge to improve current products
Developing new products in line with industry trends and target market needs
Identifying and reporting any technical issues you find when evaluating products
Overseeing tests and trials and assessing how effective processes and products are
Managing the R&D team and making sure policies and procedures are adhered to
Budgeting and forecasting new research plans and developments
Attending conferences and presenting research topics
Collaborating with market research companies to ensure products will be successful

In addition, strategic responsibilities, you will also have direct line management responsibilities to managers of the following functional Teams, on site in Uppsala:
Project management
Software development
Hardware and architecture
Verification and validation
Innovation and Process Integration

Your primary place of work will be at Biotage R&D Headquarters, in Uppsala, where you will be required to attend, in person, daily. You may also be asked to travel, when required globally.
Person Specification
Experience
Minimum 10 yrs. experience as a Researcher
Master’s Degree or Higher in a related field
Proven track record of successful R&D Projects

Skills & Knowledge
Qualitive and Quantitative Research Mastery
Excellent communication and interpersonal skills.
Strong analytical skills.
High level of problem solving and decision-making abilities.
Ability to manage a team and lead projects.
Ability to analyse and interpret data.
Ability to develop strategies and plans.
This is a highly rewarding and varied role, and we particularly encourage applicants with an extensive background in Research & Development.

ApplicationPlease submit your application no later than 31stof January 2025. The selection process will proceed as applications arrive and may be concluded before the final application date. Visa mindre

About the Role
As an Engineering Manager, you will drive the organization’s goals by empowering and engaging with the technical experts in your team, while supporting the success of a group of experienced software engineers by clearly communicating expectations, initiatives, and objectives.
You will contribute to the evolution of solutions targeting the embedded domain as part of the Engineering division. We are striving for better ways of working as well as advancing the solutions engineering model. You will accomplish this by collaborating with stakeholders across various domains, both technical and organizational. Your responsibilities will include budget preparations, full employment journey, individual coaching, and your teams’ delivery of value to stakeholders while working towards company goals.
In Engineering we work together with development of products that our customers use in their development of embedded systems. We provide customers with IDEs, debuggers, probes for connectivity to hardware devices for programming and debugging, compiles, linkers, static analysis tools, tools for state machine modelling, and plugins for VS Code and Eclipse. Additionally, we provide security solutions to protect our customers’ IP through the lifecycle of their products.
Openings in three Engineering Teams
The restructuring of our engineering department now creates openings for three new Engineering Managers to join IAR! The qualifications we are looking for are similar for all three roles, as the overall responsibility of an Engineering Manager is consistent regardless of which team you lead. The size of each team is in between 10-15 people, and all three managers will work mainly from our Uppsala office.
What differs is the product area you will be part of, as each team focuses on its own specific domain. Together with Product owners, you will be involved in leading the work within your team The technical and strategic focus areas will vary depending on the team you belong to. No matter which team you are part of, there will be a lot of cooperation together with other Engineering Managers as well. Learn more about the teams below!
Debugger devices, Probes and LMS team
This team focuses on developing and maintaining debugger technology on desktop for customer developers as well as for our probes, and adding support for hardware devices. Hardware device support in the debugger is enabling customers to connect to the right hardware in a seamless and efficient manner. This also includes work with VHDL design and software that runs on the hardware probes as well as on a PC. In addition to this, the team is responsible for our license management system, which is a product encompassing both Windows and Linux-based solutions, as well as a cloud service. The team primarily works with C and C++ in both embedded and PC environments, using modern technologies to create high-quality and scalable solutions.

Product Governance team
This international team, with members in both Sweden and Cambridge, is responsible for some of IAR's strategic functions within system architecture, product ownership, project management and product documentation. The team plays a central role in supporting the entire Engineering organization by delivering system level expertise and need to interact across, and beyond, Engineering. When applying for this role, your experience from project management, or work as a product owner in addition to leading people is more important than the technical aspects of embedded components and PC software development (see success factors for the roles below). The team works on developing and maintaining the system architecture for our solutions, while also being responsible for product documentation and system level leadership for Engineering to deliver on their commitments. In the team’s daily work they come across products and solutions developed using technologies such as C, C++, Python, Java, C#, assembler, VHDL, MFC, and Qt.

IDE team
Our IDE team develops and maintains IAR's Embedded Workbench, plugins for VSCode, and Eclipse. These are used by our customers to edit, build, debug, and analyze embedded applications. The team focuses on creating a user-friendly and efficient platform with features such as code editing, language support, and source-code-project management. The IDE team is also responsible for our VisualState product.
The work is carried out using technologies such as C++, Qt, MFC (Microsoft Foundation Classes), Java and Typescript. Their goal is to deliver a stable and smooth user experience that facilitates the development process for our customers.

Qualifications
See all qualifications on our webpage: https://www.iar.com/job-openings/engineering/manager/uppsala Visa mindre

At Galderma we're unique and we embrace difference.

Whether it's the unique breadth of our integrated offering that covers Aesthetics, Consumer, and Prescription products; or our commitment to recognising and rewarding people for the contribution they make - working here isn't like anywhere else.



At Galderma, we actively give our teams reasons to believe in our ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact.



Job Title: QA Product Quality Manager Biologics
Location: Uppsala, Sweden (hybrid)



Job Description

Join Galderma Uppsala as our QA Product Quality Manager - Biologics and lead our quality assurance program to deliver safe, effective products that meet global regulatory standards. As an experienced leader, you'll oversee QA oversight activities, support strategic expansion programs, and build a culture of excellence. You will have an important role in driving compliance, innovation, and efficiency in a GMP environment with a strong focus on aseptic processes. Be part of a dynamic team where your expertise will directly impact operational success and patient outcomes.



* Key Responsibilities
* Lead and enhance QA oversight for biologics manufacturing, ensuring compliance with market regulations and internal standards.
* Strategically support biologics expansion programs, contributing to innovation and operational excellence.
* Drive the investigation and resolution of non-conformities, ensuring QA approval and implementation of corrective actions.
* Play a key role in GMP training, focusing on aseptic competencies and quality culture.
* Manage and develop a team of QA professionals, fostering growth, succession planning, and performance.
* Participate in regulatory inspections, ensuring site compliance and readiness.



Skills & Qualifications

* Master's or Bachelor's degree in a relevant field
* Several years of experience in the life science industry
* Strong knowledge of GMP requirements and quality assurance in aseptic biologics manufacturing processes
* Passionate for developing teams, built on trust and strive for high performance
* In-depth understanding of regulatory requirements and experience with hosting and supporting inspections
* Fluency in English and Swedish, with excellent communication and collaboration skills



What we offer in return
You will be working for an organization that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.



As a new Manager at Galderma, you will participate in our Leadership programs and reflect on how you lead yourself and others. You will also join a local network of managers to discuss, exchange perspectives and get support from peers.



As Galderma's Global Center of Excellence for Aesthetics we have in Uppsala a unique edge as we have on our site the whole product chain from research and development to production and marketing. Here our nearly 600 employees work on our world leading brands such as Restylane, Azzalure and Sculptra.



We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10 minute bike ride from Uppsala Central Station.



Next steps
We welcome your application via our company website CAREERS | Galderma. If you are currently an employee of Galderma, we welcome your application via our internal career site via Workday. Apply as soon as possible though no later than the 13th of January 2025. The selection process is ongoing and the role may be filled prior the last application date.



* If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
* The next step is a virtual conversation with the hiring manager
* The final step is a panel conversation with the extended team



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do. Visa mindre

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

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

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

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

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Who we are and what we do:
At Viedoc, we design engaging software that modernizes clinical research so that necessary treatments can reach the people who need them faster.


We accomplish this by combining technology and a creative design to streamline, automate and simplify conventional processes within clinical research. Simply put, Viedoc makes every aspect of a clinical study a bit smoother, resulting in greater discoveries that make a difference, and has the potential to improve lives.

Real change means challenging the status quo – our driving force since we started almost two decades ago. In everything we do, we work for a healthier world, searching for better, more efficient solutions that answer to the needs of both our users and humanity.

We are proud to foster an inclusive workplace. We believe that diversity of experience, perspectives, and supportive work culture will lead to a better work environment for our employees and, ultimately, a better product.

What you will do and why:

We are seeking a dynamic and experienced Development Manager to join our Uppsala office. This senior role reports directly to the CTO and focuses on people development within our integrated team structure. The Development Manager will oversee developers, testers, and lead developers, ensuring smooth operations, improved ways of working, and enhanced job satisfaction. Your main responsibility is to align the ambitions of our organization with the development and growth of our development teams and team members. You are the person that keeps a close watch on the productivity and mood of our team members, while also translating and aligning our company growth strategy with individual development and growth plans.

Your key responsibilities are to:

Oversee the development and growth of approximately 25-30 direct reports.

Develop and implement strategies to improve individual employee performance and overall employee satisfaction.

Conduct one-on-ones, development talks, and salary conversations.

Act as a liaison between leadership and developers to address challenges and improve communication.

Collaborate with HR and the CTO to set up and manage training and development programs, if need be.


 
As a professional, we would like you to have:

Bachelor’s degree in Computer Science or equivalent experience.

Minimum of five to ten years of experience in the tech industry, preferably with a SaaS product.

Background as a developer or engineer in a software company, with an understanding of C# and .NET environments, and Azure Cloud (preferred but not required).

Strong leadership skills with a facilitating leadership style.

Proven ability to grow and develop individual employees, their satisfaction, retention rate, performance, and overall career development.


 
As a person, we would like you to be:


Empathetic: Understanding and relating to team members' needs and motivations

Communicative: Effective communicator between leadership and team members

Analytical: Assessing team dynamics and organizational needs

Proactive: Initiating solutions to address issues

Supportive: Encouraging and supporting professional growth

Adaptable: Flexible to changing circumstances

Resilient: Handling stress and challenges positively

Trustworthy: Building trust through integrity and transparency


Industry
eClinical, Software, Pharmaceutical, Biotech, Medical Device, Consumer Health

Interested?
If you want to join our incredible team, apply for the job! Do you want to know more? Feel free to reach out to the team member responsible for this role below. Visa mindre

Aurora Innovation?is a leading tech supplier for the healthcare sector, dedicated to increasing access to care services and creating well-functioning work environments for caregivers, using latest technology. Our modern SaaS solution for patient contact management,?Aurora teleQ, bridges the gap between patients and caregivers at a time that suits both, across channels. From our headquarters in Uppsala, local offices in Finland, Holland and Spain and together with our partners, we continuously expand our leadership into new European markets.

The healthcare market is undergoing a rapid transformation, where Aurora Innovation is a leading player in the emerging digital ecosystem. We are now looking for a driven?Head of Development to take the lead for our communications domain of Auroras product teleQ. Your expertise could be the missing piece in our tech puzzle, are you ready to contribute to a healthier world?

We are looking for a Head of Development

We are looking for a driven Head of Development for three small teams with approximately 8 people. Your team consists of talented system developers. You will report to the CTO and be a member of the IT -management team.

Who are you?

In order to thrive in this position, you must not only hold technical understanding, but you most likely also have:

Strategic and technical ability
People management, at least 2 years of experience as a leader
Strong self-management, power of initiative and prioritization skills
Background as a developer, preferably JAVA
Experience from telecom, preferable “voice” or “digital communication platforms”
Excellent communication skills in English and Swedish
A bachelor’s or master’s degree in engineering or other relevant field (or equivalent acquired skills and qualifications)


Aurora Innovation is looking for a coaching leader who can truly motivate their team as well as be a spokesperson in the domain of “Communications”.

To be successful in this role we believe that you are social, strategic and direct in your communications. You will need to be entrepreneurial and identify new ways to succeed and drive growth. It would be excellent if you have previous experience within communications (telecom).

Why this opportunity is a great one:

We are offering you a great opportunity to be a key player in Aurora Innovations growing business and continued geographical expansion
Impact: We are on a global mission to ensure our customers digital transformation to a safer and more tailormade patient journey
 We are an ambitious, competent team who support each other to constantly exceed expectations while having a fun inclusive environment
Competitive Salary and Benefits


If you're an experienced Developer with ambition to lead who's looking to join a scale-up, the timing couldn't be better. Apply right away and we'll get back to you.

Welcome to Aurora Innovation

At Aurora Innovation you will find a culture characterized by the affinity and cooperation of a family business, in combination with a fast growing technology and business environment, where the energy and the eagerness to contribute and to develop are central elements. For more than 20 years we have enabled positive, personalized experiences for people in need of care and well-functioning environments for healthcare professionals. Today we are a growing, healthy company with more than 100 employees and a turnover of approximately 160 MSEK. Our headquarters are located in modern facilities, next to the central station in Uppsala only a train commute away form Stockholm Central Station.

We hope to share our passion with you!

Contact and application

In this recruitment, Aurora Innovation collaborates with Active Search. For more information, please contact Mia Hedberg Recruitment Consultant Tel: +46707273500 or [email protected] Visa mindre

Spillvatten

Vill du vara med och bidra till utvecklingen för framtidens avloppsreningsverk och räds inte komplexiteten i en lagstyrd verksamhet med hög utvecklingstakt? Vill du utveckla ditt ledarskap och göra en betydelsefull insats för samhällsviktig verksamhet i en bransch där hållbarhet är kärnverksamhet? Sök rollen som gruppchef process och utveckling på spillvattenavdelningen.

Om tjänsten
Varje år behandlas cirka 22 miljoner kubikmeter vatten i våra avloppsreningsverk. Spillvattenavdelningen är processansvarig för att omhänderta och rena spillvatten, vilket omfattar att drifta, förvalta och utveckla anläggningar för rening av spillvatten som utgör en del av Uppsala kommuns allmänna VA-anläggning.

Nu söker vi en gruppchef till process och utveckling inom spillvattenavdelningen. Gruppen process och utveckling består av tio medarbetare vars uppdrag är att övervaka och utveckla reningsprocessen, utveckla anläggningsdelar, mätning och provtagning. Gruppen jobbar med att följa upp anläggningarnas status, genomföra projekt och åtgärdsplaner samt delta i arbetet med att utveckla strategier och arbetsprocesser. Även förstudier, tester och försök inom spillvatten, planering av kommande anläggningsdelar samt deltagande i olika samverkans- och forskningsgrupper ingår i gruppens arbete.
Som gruppchef ansvarar du för att samordna, leda och fördela arbetet inom gruppen för att uppnå verksamhetens mål och budget. Arbetsuppgifterna innefattar bl.a.:

• Personal- och arbetsmiljöansvar, inklusive medarbetar- och lönesamtal, samt planering
• Fakturahantering för inköp och löpande kostnader inom gruppen enligt delegation
• Delta som fackmässigt stöd i investeringsprojekt

Du tillhör spillvattens ledningsgrupp och rapporterar till avdelningschef. Du har din arbetsplats på Kungsängsverket, men det finns möjlighet att arbeta på våra andra kontor och till viss del på distans.

Kvalifikationer

• Relevant högskoleutbildning inom t.ex. vatten och miljö eller liknande
• Flera års erfarenhet från VA-branschen och särskilt inom spillvattenrening
• Arbetslivserfarenhet av att arbeta med reningsprocess, projektering eller VA-utredningar
• Arbetslivserfarenhet av att leda andra
• Arbetslivserfarenhet av personalansvar är meriterande

Vi lägger stor vikt vid dina personliga egenskaper och vill att du delar våra gemensamma kärnvärden, ”vi är lyhörda, framsynta och nyfikna”, samt tillämpar dem i din yrkesroll. För att trivas i rollen tror vi att du är strukturerad och ansvarstagande med förmåga att själv se vad som behöver göras, samtidigt som du styr verksamheten mot satta mål. Som gruppchef har du många interna och externa kontakter vilket innebär att du bör vara kommunikativ, flexibel och kunna skapa goda relationer och samarbeten.

Kontakt och ansökan
På grund av julledighet kommer vi att påbörja urvalet 2/1 2024, därefter gör löpande urval och intervjuer, så skicka in din ansökan så snart som möjligt, dock senast 2024-01-20. Med hänvisning till GDPR tar vi inte emot ansökningar via mail.

För mer information om tjänsten kontakta
Avdelningschef Anna Yman, tfn 018-727 96 21
HR-partner Cecilia Jansson, tfn 018-726 09 72

Övrig information
En stor del av vår verksamhet klassas som samhällsviktig verksamhet eftersom vi försörjer Sveriges fjärde största stad med dricksvatten. För denna tjänst kommer säkerhetsprövning med registerkontroll att genomföras före anställning. Du ska även vara beredd att krigsplaceras inom ramen för Uppsala Vatten och Avfalls roll i totalförsvaret. Uppsala Vatten tillämpar 6 månaders provanställning.

Om Uppsala Vatten
Välkommen till Uppsala Vatten och Avfall AB. Vårt mål är att aktivt bidra till ett hållbart samhälle. Det gör vi genom att ständigt utveckla nya resurssmarta lösningar och uppmuntra till återvinning och återbruk. Vi ger Uppsala dricksvatten, renar avloppsvatten och tar hand om regnvatten. Vi skapar kretsloppstjänster där vi gör biogas av matavfall, minskar vattenförbrukningen och återanvänder material på bästa sätt. Vi bidrar till ett cirkulärt Uppsala.

Vill du veta mer om Uppsala Vatten? Läs mer på Om oss | uppsalavatten.se (https://www.uppsalavatten.se/om-oss/) Visa mindre

Bio-Works is looking for an organized and customer-focused Development Manager to join the development and specialized production team. The team develops projects that support the pipeline of new products and applications as well as provides technical insights for other parts of the business including sales, purchasing & production.

This role will be a full-time position based in our Uppsala, Sweden site. This role is partly office based and partly laboratory based. You will have the opportunity to bring together your communication and planning skills to find the best solutions for our customers. If you have experience in organic chemistry/synthesis (Chromatography) and an analytical mindset - let’s talk!

Bio-Works Development and Specialized Production team is part of our Products unit, delivering the technology and process capability needed to operate, maintain, and improve the manufacturing operations. The team consists of 4 dedicated associates who are responsible for applied research/engineering development.

How you will thrive and create an impact;

- Successful management of a small team of 3 scientists/engineers and 1 production technician by ensuring delivery of objectives

- Manage personnel, resources, and activities in the section to fulfil short- and long-term organizational goals and priorities.

- Development of agarose-based chromatography resins and other innovative new products including initial viability discussions, development of ligand coupling and QC methods, stability, and batch testing.

- Keep up to date with current analytical methods, as well as identifying possible future trends in separation science.

- Support manufacturing department with process development, technical data, and customer complaint investigation.

- Plan and execute production of specialized products to meet delivery commitments to customers.

QUALIFICATIONS ??????????????????????????

- A degree or equivalent in organic or polymer chemistry or industry related background

- Solid previous working experience within organic chemistry/synthesis (Chromatography resins).

- Strong theoretical and practical experience in areas of developing agarose-based resins is essential.

- Knowledge of analytical methods for characterization of chromatography resins (such as titration, ÄKTA systems, dry content analysis, UV spectroscopy, microscopy etc.) is required.

- Strong project management skills are necessary.

- Business proficiency in English and good knowledge of Swedish.

- Previous working experience in a lab is ideal.

- Leadership experience is desired.

- Administrative work (review technical documentation) experience is a plus.

- Design of experiment experience is advantageous.

- Knowledge of ISO 9001 and/or GMP is meritorious.

At Bio-Works, your drivers and motivation are important. To be successful in this role you need to have excellent communication skills, both verbally and written. You need to be good at building customer relationships and be a team player and collaborator able to work towards both personal and company goals. You also need to show strong leadership qualities, such as authenticity, emotional intelligence and courage.

WHAT WE OFFER ????

In addition to a fun and challenging role, you are offered the opportunity to join a company on an exciting journey towards profitability. You will work with driven and competent colleagues and be part of the extended management team. We offer you flexibility and the opportunity to work from home in combination with on-site work as needed. You will also be able to adjust your working hours so that your personal life can flow smoothly. We have breakfast on Mondays, fika on Fridays and like spending time together over lunches and other activities.

We of course also have good benefits such as 30 days of vacation per year, ATF-hours (shortening of work hours) which we spread out over the year for some extra time off, wellness benefits, occupational pension, insurances (both collective agreement insurances and private insurances) and more.

GOOD TO KNOW ????

Start: According to agreement

Employment form: Permanent, with 6 months probation

Scope: Full time (100%, 40h/week)

Location: Uppsala (Uppsala Business Park)

Bio-Works has a collective agreement according to IKEM.

APPLICATION ????

Last application day is 2023-11-19. We do not accept applications via e-mail. We will process applications continuously which means the vacancy can be filled before the last application date, so please apply as soon as possible. The position requires you to be located in Uppsala or the vicinity. You also need to be a citizen in the EU/EEA/Switzerland region or have the authority to work in Sweden.

ABOUT US ????

Bio-Works enables scientists to achieve their purification goals, from laboratory research to large scale bioprocess production. Our vision is a biotech industry that embraces, develops and builds on new methods and novel ideas. WorkBeads™, Bio-Works’ next-generation, agarose-based products, are used to purify proteins, peptides and other biomolecules, resulting in purer therapies and safer diagnostics. Through collaboration with customers and partners, we develop purification solutions that make important medicines available and accessible to everyone. Visa mindre

Sysmex Astrego is a rapidly growing in vitro diagnostic company with a commercialized diagnostic test to determine the presence of bacteria in patient samples and resistance to various antibiotics. Our mission is to shape the advancement of healthcare. We are committed to grow as a sustainable company, creating social and economic value, and providing a greater sense of security among people and the society in which they live.
The role
Sysmex Astrego is growing and this is a new role reporting directly to Director R&D. Your responsibility is to inspire, lead, shape, and grow the software engineering team, today consisting of 7 members. You will enable the team in their daily work; ensuring that the team has a clear view of where to go, remove obstacles when required, and work closely with several stakeholders to ensure priorities are clear. You will be fully responsible for software development results.
You will support, coach and lead development in respect to agile principles, and ensure that the team’s mission, goals, scope and product domain are understood.
Ensure that teams have a defined and efficient way of working in regards to planning, work and tooling.
Inspire and help the team towards self-management to acquire new knowledge and to constantly improve.
Collaborate with product management and R&D to align product and technical objectives.

We program mostly in Python and C on an embedded Linux platform. We are taking next steps in our internal way of working, and we want to implement test-driven development with Kanban or Scrum as a working method. The development environment is in PyCharm and case management takes place in Jira. We use Git as a repo manager through BitBucket.
Your profile
You are interested in people management and leading teams, as well as helping team members to succeed. At the same time you are driven by continuously improving our way of working.
Bachelor’s or Master's degree in Computer Science or related technical field
Minimum of 3 years experience of leading engineering projects and teams
Minimum of 10 years hands-on software development experience
Previous experience of software development in medical devices or diagnostics
Strong ability to clearly communicate and interact with other departments and stakeholders
Highly structured and thorough in your daily work
Excellent communications skills in Swedish and English
Previous experience of bringing products through FDA approval is meritorious.

We offer
Sysmex Astrego is committed to creating an inclusive workplace that values diversity. We are a non-discriminatory company and give every qualified candidate the opportunity to bring their expertise and valuable contributions to the team.
Among other things we offer you:
competitive compensation package
wellness allowance
work-life balance.

To find out more about working with us: https://careers.sysmex-astrego.se/
Please note that this work is onsite at our office in Uppsala.
About us
Sysmex Astrego AB is a fast-growing and innovative company in medical diagnostics, with a vision to develop diagnostic products to contribute to the global fight against antibiotic resistance. The company’s first product is aimed at primary care for the diagnosis of urinary tract infection with suggestions for appropriate antibiotics. Visa mindre

With a unique legacy in dermatology as well as decades of cutting-edge innovation, Galderma is the leading company solely dedicated to skin and advancing the future of dermatology.

We look for people who focus on getting results, embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all, they must be passionate about doing something meaningful for consumers, patients and the healthcare professionals we serve every day. We aim to empower each employee and to promote their personal growth all the while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy and personal rights of every employee.

At Galderma, we actively give our teams reasons to believe in our ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create unparalleled, direct impact.

At Galderma we're unique and we embrace difference.

Whether it's the unique breadth of our integrated offering that covers Aesthetics, Consumer, and Prescription products; or our commitment to recognising and rewarding people for the contribution they make - working here isn't like anywhere else.

At Galderma, we actively give our teams reasons to believe in our ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact.

Galderma is looking for a Head of Medical Devices Reg Strategy to be based on our Uppsala site.



As Head of Medical Devices Reg Strategy, you will be in a global role responsible for setting strategy and driving the registration and maintenance of Galderma's portfolio of Medical Device in accordance with regulatory requirements and international quality standards. You will head the Medical Devices Regulatory Team of around 20 people, including 3 team leaders and work closely with main stakeholders including Aesthetics Business Unit, Operations, R&D, Medical Affairs and Commercial.



Key Tasks

*

Lead the team working on Regulatory Affairs activities for the Company portfolio of Medical Device products.
*

Create and drive strategies for new marketing applications worldwide.
*

Secure compliance by adequate and timely assessment and implementation of new regulatory requirements worldwide, including assessing the regulatory impact of manufacturing and other improvements/changes to Galderma's processes and where necessary notify authorities.
*

Provide regulatory guidance in general to projects and organization.
*

Guide and drive regulatory assessment of new opportunities (internal R&D candidates of Business Development external opportunities)
*

Represent Global Regulatory Affairs in the Aesthetics Global Business Unit Leadership Team/Steering Committee,
*

Champion Regulatory Device Strategy within Global Regulatory Affairs Leadership Team and with other R&D Leaders.



Skills & Qualifications

*

Industry experience with 10+ years Medical Device Regulatory Affairs needed, Class III experience preferred. Pharma Regulatory a plus
*

Has managed a Regulatory Affairs team
*

Ability to manage other stakeholders such as R&D, Operations and Commercial
*

Has worked with multiple markets and with various Notified Bodies
*

Understanding of the new Medical Device Regulations (MDR)
*

Knowledge of Medical Device Single Audit Program (MDSAP)
*

Entrepreneurial mindset and can-do attitude



What we offer in return



As Galderma's Global Center of Excellence for Aesthetics we have in Uppsala, a unique edge as we have on site the whole product chain from research and development to production. Here, our nearly 450 employees work on our world leading brands such as Restylane and Sculptra.



We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10-minute bike ride from Uppsala Central Station. Visa mindre

Avdelningen för ekonomi och styrning

Region Uppsala ska främja hälsa och förbättra livskvaliteten hos invånarna. Region Uppsala tar fasta på förmåga till förnyelse och tar ansvar för en hållbar utveckling. Region Uppsala arbetar för ett gott liv i en nyskapande kunskapsregion med internationell lyskraft. En nyskapande region, en växande region – en region för alla.

Regionkontoret ska stödja den politiska ledningen och förvaltningarna så att den politiska inriktningen får genomslag i regionens olika verksamheter och Region Uppsala kan axla sin roll, regionalt och nationellt. Regionkontoret utgör regiondirektörens resurser i att bereda ärenden, verkställa beslut och uppdrag, samordna verksamheter internt inom den samlade förvaltningsorganisationen samt samarbeta externt med kommuner och andra viktiga parter.

Vår verksamhet
Region Uppsala har en centraliserad inköps- och upphandlingsenhet som förutom Regionens egna upphandlingar också ansvarar för att på uppdrag från Varuförsörjningsnämnden genomföra upphandlingar och försörja fem regioner med förbrukningsmaterial. De fem regionerna är Uppsala, Västmanland, Sörmland, Örebro och Dalarna. Totalt uppgår inköpen till ca 8 miljarder kronor per år.

Regioninköp och upphandling finns organisatoriskt placerad på Regionkontoret inom Avdelningen för ekonomi och styrning. På enheten arbetar i dag ett fyrtiotal medarbetare fördelat på tre upphandlingsgrupper och en stab.

Region Uppsala har beslutat att införa kategoristyrt arbetssätt och under de kommande åren kommer vi att fokusera på att utveckla vår verksamhet i den riktningen.

Vi söker nu en stabs-och utvecklingschef till vår enhet. Rollen som stabs- och utvecklingschef är ny och har en tydlig inriktning på utveckling av upphandlingsmodeller och metoder för både Regioninköp och upphandling inom Region Uppsala samt Varuförsörjningen.

Ditt uppdrag
Du kommer att ansvara för metodutveckling av upphandlingsmodeller samt för utveckling och utbildning av enhetens samtliga upphandlare avseende tillämpning av lagen om offentlig upphandling, lämpliga upphandlingsmodeller och utvärdering.

I uppdraget ingår att vara ansvarig för framtagning av modeller för uppföljning och ansvarsutkrävande. Du kommer att företräda Region Uppsala samt Varuförsörjningsnämnden vid förhandlingar av olika slag och vid tvister. Du kommer att driva överprövningsprocesser och ser detta som ett viktigt sätt att pröva dina nya modeller och etablera ny praxis.

Du kommer att ha personalansvar för staben som består av ca 10 medarbetare. Staben leder och samordnar den strategiska planeringen och beslutsunderlag till stöd för förvaltnings- och upphandlingschefen. Som stabs- och utvecklingschef ingår du i den gemensamma ledningsgruppen för Regioninköp och upphandling samt Varuförsörjningen.

En viktig del av ditt chefsuppdrag är att skapa samhörighet i gruppen och samsyn kring uppdrag och mål. Som chef inom Region Uppsala förväntas du vara coachande, utöva ett situationsanpassat ledarskap och verka för en hälsofrämjande arbetsplats där medarbetarna trivs och utvecklas.

Dina kvalifikationer
Du har en jur.kand/juristexamen, med tidigare erfarenhet från ledande roll. Du har lång erfarenhet av utveckling av upphandling, utvärderingsmodeller och fördelningsnycklar. Du har domstolserfarenhet och vana att driva avtalsrättsliga och entreprenadtvister i domstol.

Du har lång erfarenhet av att utbilda och utveckla upphandlare avseende tillämpning av lagen om offentlig upphandling samt gällande upphandlingsmodeller.

Du har B-körkort samt goda kunskaper i svenska, både muntligt och skriftligt.

Din kompetens
Du är en trygg och erfaren ledare, med god förmåga att skapa delaktighet och engagemang samt skapa förutsättningar för att effektivt nå gemensamma mål. Du har intresse av att utveckla både verksamheten och medarbetarna, du trivs när du ser dina medarbetare växa.

Du är nytänkande och kreativ och utmanar gärna nuvarande och etablerade metoder och upphandlingsmodeller för att finna helt nya vägar för att nå framgångsrik upphandling. Du har specialistkunskap inom lagen om offentlig upphandling och underhåller kontinuerligt din kunskap samt är en kunskapsresurs för andra.

Stor vikt läggs vid personliga egenskaper.

Vi erbjuder
Tillsvidareanställning på heltid, med tillträde enligt överenskommelse.

Inom Region Uppsala har alla chefer och ledare en viktig roll. Genom dig som chef kan medarbetare växa och bidra till ännu bättre service för medborgarna. Vi vill ge våra ledare rätt förutsättningar att lyckas i sin roll. Därför erbjuder vi bland annat flera ledarutbildningar för våra chefer.

Vårt moderna kontor ligger mitt i centrala Uppsala, i direkt anslutning till Uppsala resecentrum.

Som arbetsgivare vill vi skapa förutsättningar för att våra medarbetare ska ha det bra, så att man kan känna sig trygg och ha kvalitet i livet utanför jobbet. Förutom att vi har ett av Sveriges bästa kollektivavtal erbjuder vi subventionerade UL-biljetter och ett förmånligt friskvårdsbidrag. Vi erbjuder också våra medarbetare en flexibel arbetsplats, med möjlighet att arbeta delvis på distans utifrån överenskommelse.

Hos oss får du förmåner som gör skillnad, läs om förmånerna här (https://regionuppsala.se/jobba-hos-oss/bli-var-nya-kollega/formaner/).

Vill du veta mer?
Kontakta upphandlingschef Jonas Arvidsson, 018-617 59 45, vid frågor om tjänsten och HR-partner Towe Jansson Wahlnäs, 018-617 49 91 vid frågor om rekryteringsprocessen.

Fackliga representanter: Vision - Christianne Simson, 018-611 32 51. SACO - Leif Sandberg, 0706-741088. Övriga fackförbund nås via Region Uppsalas växel 018-611 00 00.

Vill du jobba med oss?
Välkommen med din ansökan via länken nedan.

Region Uppsala värdesätter de kvaliteter som jämn könsfördelning och mångfald tillför verksamheten. Vi ser därför gärna sökande av alla kön och med olika födelsebakgrund, funktionalitet och livserfarenhet.

Denna rekrytering sker helt genom Region Uppsalas försorg. Vi undanber oss därför telefonsamtal från rekryteringsföretag och annonsförsäljare. Visa mindre

Sjukhusadministrationen

Vi är Akademiska sjukhuset – ett av Sveriges ledande universitetssjukhus. Förutom rollen som länssjukhus är vi leverantör av högspecialiserad vård och betjänar två miljoner människor i Mellansverige. Hos oss pågår det något hela tiden – ett nytt liv ser dagens ljus, en mormor opereras, en kollega hyllas som livets hjälte. Vi tror att ärlighet varar längst och det är ingen hemlighet att vi behöver bli fler. Som kollega till oss får du vara med om mycket. Hårda prövningar men också fantastiska händelser, stark gemenskap och stöttning från kollegor och medmänniskor. För att se delar ur vår verklighet, besök vår fotoutställning på akademiskafotoutstallning.se.

Välkommen med din ansökan och bli en del av oss.

Vår verksamhet
Enheten för digital utveckling inom Akademiska sjukhusets sjukhusadministration ansvarar för nedbrytning av regionens och sjukhusets strategier i en sammanhållen arkitektur, gör analyser, bidrar till styrning av utveckling och balanserar taktiska och strategiska initiativ i ett helhetsperspektiv. Nu söker vi dig som vill ansvara för det spännande arbetet med att leda och styra Akademiska sjukhusets fortsatta digitalisering.

Ditt uppdrag
Du kommer att arbeta nära sjukhusledning och beslutsfattare över hela verksamheten för att hjälpa organisationen att möta nya omvärldskrav, bidra till strategiska förflyttningar samt säkerställa att verksamheten utvecklas i enlighet med våra strategier och mål. Du leder och samordnar arbetet i nära samarbete med dina medarbetare på enheten för digital utveckling och andra enheter inom sjukhusadministrationen. Som chef för enheten leder, fördelar och utvecklar du arbetet inom enheten. Där ingår budgetansvar och personalansvar för enhetens medarbetare.

Avgörande för att lyckas i rollen är att du driver utvecklingen inom området och etablerar ett strukturerat processbaserat arbetssätt för utveckling på hela sjukhuset. Du kommer att stödja projekt och andra initiativ att lyfta blicken från aktuell leverans till ett helhetsperspektiv för att nå sjukhusets mål. Digitala funktioner och system har en central roll i sjukvårdens fortsatta verksamhetsutveckling. Du kommer att ha en viktig roll från det inspirerande arbetet med vision, strategi och målbild till det komplexa arbetet med införandet av nya system och tekniker.

Dina kvalifikationer
Vi söker dig som har högskole-/universitetsexamen inom relevant område och gärna akademisk kompetens på magister-/masternivå. Du har en gedigen bakgrund inom IT-området och erfarenhet av att leda utvecklings-och förändringsarbeten. Du har erfarenhet av att driva digital utveckling och förändringsarbete i såväl stora eller komplexa organisationer som i offentlig verksamhet. Vidare har du god förmåga att leda och driva grupper samt prioritera aktiviteter utifrån given målbild.

Din kompetens
Du besitter en pedagogisk förmåga att presentera och förklara beroende på vem eller vilka som är mottagare. Du är lösningsorienterad i ditt förhållningssätt och har en god förmåga att kommunicera och entusiasmera för nya idéer och utveckling. Du har ett genuint intresse för kvalitets- och förbättringsarbete och stimuleras av att arbeta tillsammans med andra. Du är strukturerad och har en förmåga att prioritera och samtidigt se helheten.

Vi erbjuder
Tjänsten är en tillsvidaretjänst på heltid med tillträde enligt överenskommelse. Hos oss får du förmåner som gör skillnad, läs om förmånerna här (https://regionuppsala.se/jobba-hos-oss/bli-var-nya-kollega/formaner/).

Vill du veta mer?
Frida Antesson, administrativ direktör, 018-611 57 45
Hans Natvig, enterprise architect, 018-617 03 39
Fackliga företrädare nås via växeln 018-611 00 00

Vill du jobba med oss?
Välkommen med din ansökan via länken nedan.

Region Uppsala värdesätter de kvaliteter som jämn könsfördelning och mångfald tillför verksamheten. Vi ser därför gärna sökande av alla kön och med olika födelsebakgrund, funktionalitet och livserfarenhet.

Denna rekrytering sker helt genom Region Uppsalas försorg. Vi undanber oss därför telefonsamtal från rekryteringsföretag och annonsförsäljare. Visa mindre

About this role:
The Director of Operations is accountable for the operational performance of the business; delivering the financial plan; shaping and executing company strategy as well as developing the team and the site to meet future growth plans. Furthermore, the role will provide people leadership and act as Company Representative to internal and external stakeholders.
The site operations include both delivery of customer projects based on our cutting-edge product portfolio and the development of new technologies as well as manufacturing of satellites and products and its supporting processes.
The Director will continue to grow the highly skilled team currently consisting of 30 persons with various engineering competencies to further deliver a revenue growth that last year exceeded 40%.
Responsibilities will include:
· Provide leadership of the site including load and capacity and organisational structure
· Accountable for all operational performance metrics (safety, quality, cost, people and delivery)
· Deliver the financial plan
· Company representative to external stakeholders and customers
· Setting strategic direction for the site
Skills Required:
· Financial and commercial acumen
· KPI Setting, delivery and management
· Ability to motivate the team and achieves goals through the work of others
· Professionalism and strong work ethic
· People Leadership skills
· Experience in product and production systems for space or other industrial applications
· Ability to interact with key internal and external stakeholders in country and globally
Why AAC Clyde Space
· A unique opportunity to become a part of shaping and growing one of the world leading companies in the fast-growing space industry
· Join, lead and develop a very highly skilled team of colleagues
· We are working on a daily basis to ensure that space technology works to the benefit of the Earth and space environment
This position is available to fill immediately, so applicants are encouraged to reply promptly with CV and covering letter.
As part of our recruitment process, we collect and process personal data relating to job applicants. We are committed to being transparent about how we collect and use this data, please click here to see our job applicant privacy notice.
For further information please contact Peter Ternebring, Recruiter, +46 70 639 88 89.
About AAC Clyde Space
AAC Clyde Space, a leading New Space company, specialises in small satellite technologies and services that enable businesses, governments, and educational organisations to access high-quality, timely data from space. This data has a vast range of applications, from weather forecasting to precision farming to environmental monitoring, and is essential to improving our quality of life on Earth.
Our growing capabilities bring together three divisions:
· Space Data as a Service – delivering data from space directly to customers
· Space missions – turnkey solutions that empower customers to streamline their space missions
· Space products and components – a full range of off-the-shelf and tailor-made subsystems, components, and sensors
AAC Clyde Space aims to become a world leader in commercial small satellites and services from space, applying advances in its technology to tackle global challenges and improve our life on Earth.
Some of our clients include Horizon Technologies, Orbcomm, NSLComm, OHB Sweden, Intuitive Machines, Orbital Micro Systems, the United States Airforce Academy, Swedish National Space Agency, UK Space Agency, European Space Agency and NASA.
AAC Clyde Space’s main operations are located in Sweden, the United Kingdom, the Netherlands, the USA and South Africa, with partner networks in Japan and South Korea. Visa mindre

Medborgarskolan är en ideell organisation som skapar mötesplatser för dig som söker kunskap, utveckling och upplevelser. Vår verksamhet inspirerar till lustfyllt och livslångt lärande. Våra kärnvärden är individen i centrum, utveckling i samverkan, ömsesidig respekt och kunskapens egenvärde.

Medborgarskolan består av förbundskansliet, som är placerat i Uppsala, och åtta regioner. På förbundskansliet finns cirka 30 medarbetare.


Medborgarskolan strävar efter att alltid uppfylla och helst överträffa våra kunders och övriga intressenters förväntningar. Ett led i det arbetet är att vidareutveckla vårt systematiska kvalitetsarbete. Arbetet i kvalitetsfunktionen bedrivs i nära samarbete med regionerna.

Om tjänsten
Som kvalitets- och utvecklingschef leder du en grupp med fyra medarbetare och har personal- och budgetansvar. Du har ett coachande förhållningssätt och frigör potentialen hos dina medarbetare genom att skapa en arbetsmiljö med engagemang och motivation. Du drivs av utveckling och gillar förändring som möjliggör ny potential såväl för medarbetare som organisation. Du är en del av förbundskansliets ledningsgrupp.

I dina arbetsuppgifter ingår också att leda Medborgarskolans strategiska kvalitetsutveckling, vilket bland annat innebär att ansvara för utvecklingen av kvalitetsarbetet inom folkbildningsverksamheten och ansvara för och ge stöd åt arbetet med villkorad uppföljning av densamma. Vidare samordnar du nationella grupper, ger stöd åt och utvecklar utbildningar inom etik och kvalitetsområdet samt ansvarar för upprättande av rutiner inom kvalitetsledningssystemet.

Vi söker dig som är kommunikativ och genuint intresserad av att arbeta proaktivt, prestigelöst och i nära dialog med verksamheten. Du är drivande och självgående i ditt uppdrag och för att kunna driva arbetet framåt behöver du också vara målfokuserad och ha förmågan att både leda och inspirera andra. Du behöver kunna lyfta blicken och ha ett helhetsperspektiv över verksamheten. Som person är du strukturerad och noggrann.

Kvalifikationer
Du har för tjänsten relevant högskoleutbildning eller motsvarande som arbetsgivaren bedömer relevant, gärna också utbildning inom projektledning samt ledarskapsutbildning. Du har några års erfarenhet av att både projektleda och också operativt arbeta med verksamhetsutveckling kopplat till kvalitet inklusive villkors- och regelefterlevnad. Det är också meriterande om du har några års erfarenhet från arbete inom studieförbund eller annan idéburen verksamhet. Erfarenhet av verksamhet med offentlig finansiering samt av att ansöka om projektmedel är också ett plus. Du har en mycket god förmåga att uttrycka dig på svenska såväl i tal som i skrift.

Tjänsten är en 100 % tillsvidaretjänst med sex månaders provanställning och är placerad vid förbundskansliet i Uppsala. Medborgarskolan är en arbetsplats som värdesätter mångfald, vi välkomnar därför sökanden med olika bakgrund.

Om du har några frågor är du välkommen att höra av dig till Ann-Sofie Olding, förbundschef 018-569502 eller Marie Nyborg, HR 018-569539.

Välkommen med din ansökan senast 2022-03-27. Visa mindre

Be part of something altogether life-changing
Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.
We are now looking for a Section Manager – Project Management Manufacturing for the large-scale chemical & biological batch manufacturing. You will be a critical part of our Process & Digital Support team of 60 employees supporting the entire manufacturing at the Uppsala site. Do you have a passion for project execution and people development? Then we would love to hear from you.
What you’ll do
Be the direct manager for our team of excellent and experienced project leaders within manufacturing.
Develop and execute the strategy & operational plan for the section, including budget responsibility.
Coach and support individual project leaders in their continued personal development and refined project execution skills.
Secure project leaders for new product introductions, production development projects as well as digital manufacturing projects in accordance with business needs.
Review project progressions and ensure critical project milestones deliveries from a business and global supply chain perspective.
Ensure project to project lessons learnt and continuous improvements.

Who you are
Master’s degree in Chemical/Biotechnology/IT-engineering or equivalent relevant field.
Minimum 10 years of experience from Life Sciences industry.
Excellent skills at leading and developing people and teams.
Previous experience from project management.
Previous experience from a people leader position.
In order to succeed in this position, you need to be highly motivated, result-oriented, creative and with a strong collaborative attitude, focusing on both internal and external customer needs and the bigger picture.
Swedish and English both required as working languages

Our business is growing quickly and we hire across the board. Interview and selection will happen continuously. We look forward to hearing from you!
When you join us, you’ll also be joining Danaher’s global organization, where 69,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.
If you’ve ever wondered what’s within you, there’s no better time to find out. Visa mindre

Does software development of image processing and analysis tools catch your eye? How about working in an innovative company within the global Life Science sector where your work contributes to improving drug development of the future?

At Antaros Medical, we value competence and development as well as ideas and creativity. We are now looking for our next experienced Software Developer to join our development team in Malmö.

As a Software Developer, you will join a team of software developers and specialists in image processing and image analysis. You will be responsible for designing and developing tools for management, processing and analysis of medical MR and PET images acquired in clinical trials. You will also be member of cross-functional project teams in clinical trials, coordinating software development solutions in the project.

In addition, your work role will include software development support to specialists with rapid prototyping and implementation of method development in advanced image analysis.

Your main responsibilities will be:

- Development, maintenance and documentation of validated software for medical image management, processing, and analysis.

- Collaborate with cross-functional clinical trial teams to understand software needs and design and implement high quality solutions to problems.

- Continuous improvement of team processes and tools.

Who are we looking for?

We believe that you have been working with professional software development, preferably with medical images in a GxP or medical device setting, for at least 4 years. You are keen on working both independently as well as in teams, communicate well verbally and in writing and thrives in a fast-paced and dynamic environment. You can design and develop advanced yet simple solutions to complex problems in collaboration with other team members that fulfils industry standard quality requirements.

Requirements:

- 4+ years’ experience of professional software development

- B.Sc. degree in relevant field

- Python

- Experience in medical image processing

In addition, we perceive professional knowledge of DICOM, Matlab, C++, Deep learning and/or AWS, to be of advantage in the work role. Experience of GxP or medical device development is also meriting.

Are you interested?

Great to hear! Please submit your application via this link along with your CV included, no later than February 10th, 2022

For more information about the position, please contact Carl Sjöberg, Manager Software Development, [email protected] +46 73 050 04 69

The recruitment is for a permanent employment.

We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical.

About Antaros Medical

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We are specialised in cardiorenal & metabolic diseases and oncology.

We combine ground-breaking imaging with profound experience in drug development and a deep knowledge in disease mechanisms. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST. Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. Visa mindre

Are you interested in image analysis in clinical trials? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this catches your interest, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

To deliver on our commitments, we are looking for people with both broad and deep experience in clinical drug development as well as project management.

As a Clinical Trial Coordinator, you will be responsible for coordination in and administration of our clinical trials. The position will be located in our office in Uppsala.

Main responsibilities:

- Provide general administrative support and assistance to the internal project team, primarily the Project Manager.
- Support the internal project team with ongoing conduct of studies including coordination of administrative tasks during the study process
- Contribute to applications & submissions by handling clinical-regulatory documents
- Assist in contact with clinical sites for specific requests (e.g., enrollment updates, missing documentation, meeting arrangements).
- Attend project team meetings and generate meeting minutes.
- Set up, organize, and maintain clinical study documentation in the trial master file
- Quality control of and archival of the TMF after final study
- Collaboration with third-party archive vendor


Requirements:

- Experience from working with clinical trials and according to ICH-GCP
- Level of education that supports skills and capabilities of the position and ensures successful conduct of responsibilities
- Collaboration skills in order to engage with people and clients
- Proven administrative skills
- Excellent knowledge of spoken and written Swedish and English


More information

For more information about the position, please contact Neha Mehta , +46 76-111-0659, or [email protected].

Please submit your application via this link with a short personal letter and your CV included, no later than February 10th 2022. We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical.

About Antaros Medical
At Antaros Medical, we are specialised in cardiometabolic diseases (including NAFLD/NASH and chronic kidney disease) and oncology. We have established ourselves as a strategic development partner to the pharmaceutical industry, where we combine ground-breaking imaging with profound experience in drug development and deep knowledge in disease mechanisms. Our projects cover clinical trials in all stages of drug development, and we work both with small biotech companies as well as global big pharma companies. We currently have around 90 employees working at our offices in Mölndal and Uppsala. Visa mindre

Trygghet, brottsförebyggande och säkerhet

Trygghet, brottsförebyggande och säkerhet söker en utvecklingsledare välfärdsbrott. Bidragsfusk och olika brott mot välfärdssystemen kostar årligen samhället stora summor. Uppsala kommun arbetar därför aktivt mot välfärdsbrott i nära samverkan med polisen och flera statliga myndigheter och tar nu ett ytterligare steg för att stärka arbetet.

Vill du ha ett omväxlande och meningsfullt arbete där du har möjlighet att bidra till att skapa ett tryggt och säkert samhälle? Då är jobbet inom Uppsala kommun något för dig. Vi vågar tänka stort, visa handlingskraft och med tillit låta nya idéer växa till hållbara lösningar.

Hos oss kommer du tillsammans med engagerade kollegor ges utvecklingsmöjligheter, samtidigt som ditt arbete bidrar till att öka tryggheten och minska brottsligheten inom kommunen och i tydliga och långsiktiga samarbeten mellan myndigheter. Enheten tar också fram beslutsunderlag, lägesbilder, rapporter, styrdokument, orsaksanalyser och utredningar inom trygghets- och säkerhetsområdet, samt verkar kunskapshöjande och stödjande för kommunens olika verksamheter genom, workshops, riskanalyser och vägledning. Enheten för trygghet, brottsförebyggande och säkerhet ansvarar även för personsäkerhet för kommunanställda och förtroendevalda samt ansvarar för kamerabevakning och ordningsvakter.

Läs mer om vår verksamhet här: Uppsala kommun (https://www.uppsala.se/)

Ditt uppdrag
Att arbeta som utvecklingsledare på enheten Trygghet, brottsförebyggande och säkerhet innebär i första hand att ansvara för det kommunövergripande arbetet kring välfärdsbrott genom att kartlägga, starta, utveckla samt samordna olika insatser och aktiviteter. Dessutom kommer du att ta nya initiativ, driva frågor framåt och presentera åtgärder, förslag och analyser inom området, samt omvärldsbevaka både internt och externt. Du kommer också aktivt att medverka och driva frågor inom enhetens övriga områden gällande trygghet, brottsförebyggande och säkerhetsarbete. Uppdraget omfattar både operativt och verksamhetsnära arbete samt strategisk planering.

Din bakgrund
Vi vänder oss till dig som har gedigen erfarenhet och bredd av såväl strategiskt arbete, som utredningsarbete mot ekonomisk och/eller organiserad brottslighet. Du har akademisk/högskoleutbildning och/eller annan utbildning som arbetsgivaren bedömer vara relevant för tjänsten. Alternativt annan utbildning i kombination med erfarenhet som arbetsgivaren bedömer relevant för tjänsten.
Du har även erfarenhet av att leda och samordna i komplexa uppdrag. Arbetet kräver även goda muntliga och skriftliga kunskaper i svenska, goda kunskaper i Office-paketet samt goda kunskaper i engelska. Det är meriterande om du har erfarenhet av arbete inom statlig myndighet eller kommun och arbete som utvecklingsledare eller har utbildning inom ledarskap.

Du har förmåga till helhetssyn och att se frågor i ett större perspektiv. Vidare är du kommunikativ och du har lätt för att lyssna och anpassa ditt sätt att kommunicera. Vi ser även att du är kreativ och ofta kommer med idéer och nya angreppssätt i arbetsrelaterade frågor. Sist men inte minst är du bra på att skapa, underhålla och utveckla arbetsmässiga relationer.

Upplysningar
I Uppsala kommun värnar vi om varandras hälsa och arbetsmiljö. Vi förväntar oss därför att du är vaccinerad mot Covid-19.

Har du frågor om tjänsten eller rekryteringsprocessen, kontakta:
Sofia Westring, enhetschef, 018-727 64 15

Fackliga företrädare:
Akavia, Jonny Eliasson, 018-727 22 12
Akademikerförbundet SSR, Maria Persson, 018-727 24 24


Har du frågor gällande registrering av din ansökan, kontakta enheten för kompetensförsörjning: 018-727 23 02.

Tjänsten är placerad i säkerhetsklass och säkerhetsprövning med registerkontroll kommer därför att genomföras före anställning.

I din ansökan ska du ange medborgarskap. Om du inte är medborgare i Sverige, EU, EES eller Schweiz måste du också kunna styrka att du har ett giltigt arbetstillstånd eller är undantagen från skyldigheten att ha arbetstillstånd. Anställning kan ske först efter kontroll av arbetstillstånd, vilket krävs enligt utlänningsförordningen.

Om vår organisation
Välkommen till kommunledningskontoret. Här jobbar du tillsammans med medarbetare på staber för kommunikation, HR, IT, ekonomi och fastighet samt avdelningarna kvalitet och planering, hållbarhet, trygghet, säkerhet och beredskap, kansli samt enheten för omvärld och ledningsstöd. På kommunledningskontoret ligger även organisationerna för näringsliv och destination samt gemensam service. Kommunledningskontoret är länken mellan våra förtroendevaldas beslut och kommunens alla verksamheter. Vårt uppdrag är bland annat att samordna och driva övergripande frågor inom demokrati, samhälls- och näringslivsutveckling samt ekologisk och social hållbarhet.

Mer information om vår organisation hittar du på uppsala.se (https://www.uppsala.se)
Vi undanber oss erbjudanden om annonserings- och rekryteringshjälp.

Dina personuppgifter kommer att användas för att administrera din ansökan inom Uppsala kommun. Visa mindre

Fresenius Kabi är ett globalt, marknadsledande företag specialiserat på klinisk nutrition, infusionsterapi och medicinsk teknik.

Fresenius Kabi står för framsteg och kvalitet i utvecklingen av innovativa produkter och tjänster för terapi och vård av kroniskt och svårt sjuka människor - på och utanför sjukhus. Våra produkter och tjänster räddar och skyddar liv samt bidrar till att förbättra människors livskvalitet.

Under mottot ”Caring for life” sätter Fresenius Kabi människan i centrum, som patient, kund och medarbetare.


Avdelningen Technology Transfer ett litet och viktigt team bestående av drivna och ambitiösa projektledare där du är med och driver utvecklingsprojekt från idé till industrialisering tillsammans med tredje part eller globala team inom Fresenius. Avdelningen ingår i Technical Operations där du kommer att tillhöra och verka i ledningsgruppen. Du tillsammans med din avdelning har en nyckelroll i den långsiktiga produktportföljen och har direktpåverkan på Fresenius Kabis framtid.

Arbetsuppgifter

Ge projektledare inom din avdelning och från andra delar av verksamheten rätt förutsättningar att följa projektprocesserna.
Mäta, visualisera och kontinuerligt förbättra projektprocesserna.
Regelbundet följa upp projektstatus och status för projektportföljen från idé till genomfört projekt.
Att leda och utveckla avdelningens arbete.
Om dig

Vi tror att du är ingenjör med lång erfarenhet av projektledning och projektportföljstyrning. Du har arbetat i chefspositioner tidigare och älskar att vara ledare. Erfarenhet av GMP är meriterande. Du talar och skriver flytande svenska och engelska.

För att bli framgångsrik som chef för Technology Transfer är du en person med ett tydligt ledarskap, starkt engagemang, driv och resultatfokus. Du är inte rädd för att fatta beslut och vill ständigt arbeta med utveckling. Du brinner för lagarbete, projektarbete och ser det som en utmaning att ta fram det bästa hos dina medarbetare.  Förtroende får du genom en öppen och ärlig dialog. Om du dessutom är analytisk och samarbetar väl över avdelningsgränserna så är du rätt person för tjänsten.

Om tjänsten

Tjänsten är en visstidsanställning i prövosyfte som efter 6 månader övergår i tillsvidareanställning efter överenskommelse. Tillträde omgående. Placeringsort är Uppsala.

Om oss

Vi är ett växande företag med cirka 1100 anställda i Sverige, och över 37 000 anställda världen över. Vi är stolta över våra produkter och det genomsyrar hela företaget. I våra medarbetarundersökningar lyfts kollegorna, utvecklingsmöjligheterna och den familjära stämningen upp som några av de bästa sakerna med att arbeta på Fresenius Kabi.

Att vara en del i Fresenius Kabi är synonymt med att vara en del i en miljö med framtidsutsikter. Vi tror på vår personal och är passionerad i vår utveckling av alla våra medarbetare. Vår världsomfattande utsträckning innebär att där finns en stor variation av vägar att välja som ett led i din framtida utveckling.

Kontakt

Vill du veta mer om tjänsten är du välkommen att kontakta Aram Yildiz 018–644 250. Fackliga kontaktpersoner är Frank Glackin för Unionen, 018–644 773 och Linda Holm för SACO, 018–644 195.

Välkommen med din ansökan via länken nedan, urval och rekrytering kan komma att ske löpande. Vi tar inte emot ansökningar via e-mail eller post Visa mindre

Are you interested in medical images and image analysis? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A company, where you would contribute and be a part of a collaborative team? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We have currently around 90 employees working at our offices in Sweden in Mölndal and Uppsala, as well as a newly established subsidiary in the US, and we are continuously growing and developing. As a part of our growth journey, we are looking for our next analytical and detail-focused Image Analyst to join our Corelab Team in Uppsala.

As an Image Analyst, you will be responsible for delivering high quality measurements and analyses of the imaging scans from MR and PET investigations, which is a core output from our company. You will work in a team that together analyses and delivers data for the clinical study. Your responsibility also includes quality control of such images and communication with imaging centres on image quality. The job environment is highly focused on research and technical development, and requires collaboration within the internal project team as well as with national and international clients and imaging centres.

Your main responsibilities will be:

- Quality control of the imaging scans and related documentation from the MR and PET investigations in the clinical trials
- Segmentation and analysis of the imaging scans from the MR and PET investigations including documentation
- Compiling results from image analysis and report back to clients according to agreed timelines
- Development, maintenance, and archiving of study documentation


Who are we looking for?

We emphasise personal suitability, and believe that you are a structured and thorough person with attention to details, who strives in an environment where high demands are placed on quality. We further believe that you are a service-oriented person who enjoys collaborating with others, as well as working individually.

We are happy to see that you have an interest in images, image analysis, technology and medicine.

Desired qualifications and skills:

- At least high school grade or equivalent, preferably in natural science. We perceive it as an advantage if you have university- or relevant higher education as biomedical scientist or similar.
- Demonstrated computer proficiency (programming skills are meritorious)
- Good knowledge of spoken and written Swedish and English


Understanding of and/or experience from working with clinical trials is considered an an advantage, including knowledge of ICH-GCP. We further perceive it as beneficial if you have skills and interest in programming.

Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than January 31, 2022. Interviews can take place during the advertisement period.

For more information about the position, please contact Anna Ringheim Cadete, Corelab Manager, at +46 73 233 00 03 or [email protected].

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/) Visa mindre

Does software development of image processing and analysis tools catch your eye? How about working in an innovative company within the global Life Science sector where your work contributes to improving drug development of the future?

At Antaros Medical, we value competence and development as well as ideas and creativity. We are now looking for our next experienced Software Developer to join our development team in Malmö.

As a Software Developer, you will join a team of software developers and specialists in image processing and image analysis. You will be responsible for designing and developing tools for management, processing and analysis of medical MR and PET images acquired in clinical trials. You will also be member of cross-functional project teams in clinical trials, coordinating software development solutions in the project.

In addition, your work role will include software development support to specialists with rapid prototyping and implementation of method development in advanced image analysis.

Your main responsibilities will be:

- Development, maintenance and documentation of validated software for medical image management, processing, and analysis.

- Collaborate with cross-functional clinical trial teams to understand software needs and design and implement high quality solutions to problems.

- Continuous improvement of team processes and tools.

Who are we looking for?

We believe that you have been working with professional software development, preferably with medical images in a GxP or medical device setting, for at least 4 years. You are keen on working both independently as well as in teams, communicate well verbally and in writing and thrives in a fast-paced and dynamic environment. You can design and develop advanced yet simple solutions to complex problems in collaboration with other team members that fulfils industry standard quality requirements.

Requirements:

- 4+ years’ experience of professional software development

- B.Sc. degree in relevant field

- Python

- Experience in medical image processing

In addition, we perceive professional knowledge of DICOM, Matlab, C++, Deep learning and/or AWS, to be of advantage in the work role. Experience of GxP or medical device development is also meriting.

Are you interested?

Great to hear! Please submit your application via this link along with your CV included, no later than January 10th, 2022

For more information about the position, please contact Carl Sjöberg, Manager Software Development, [email protected] +46 73 050 04 69

The recruitment is for a permanent employment.

We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical.

About Antaros Medical

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We are specialised in cardiorenal & metabolic diseases and oncology.

We combine ground-breaking imaging with profound experience in drug development and a deep knowledge in disease mechanisms. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST. Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. Visa mindre

Does software development of image processing and analysis tools catch your eye? How about working in an innovative company within the global Life Science sector where your work contributes to improving drug development of the future?

At Antaros Medical, we value competence and development as well as ideas and creativity. We are now looking for our next experienced Software Developer to join our development team in Uppsala.

As a Software Developer, you will join a team of software developers and specialists in image processing and image analysis. You will be responsible for designing and developing tools for management, processing and analysis of medical MR and PET images acquired in clinical trials. You will also be member of cross-functional project teams in clinical trials, coordinating software development solutions in the project.

In addition, your work role will include software development support to specialists with rapid prototyping and implementation of method development in advanced image analysis.

Your main responsibilities will be:

- Development, maintenance and documentation of validated software for medical image management, processing, and analysis.

- Collaborate with cross-functional clinical trial teams to understand software needs and design and implement high quality solutions to problems.

- Continuous improvement of team processes and tools.

Who are we looking for?

We believe that you have been working with professional software development, preferably with medical images in a GxP or medical device setting, for at least 4 years. You are keen on working both independently as well as in teams, communicate well verbally and in writing and thrives in a fast-paced and dynamic environment. You can design and develop advanced yet simple solutions to complex problems in collaboration with other team members that fulfils industry standard quality requirements.

Requirements:

- 4+ years’ experience of professional software development

- B.Sc. degree in relevant field

- Python

- Experience in medical image processing

In addition, we perceive professional knowledge of DICOM, Matlab, C++, Deep learning and/or AWS, to be of advantage in the work role. Experience of GxP or medical device development is also meriting.

Are you interested?

Great to hear! Please submit your application via this link along with your CV included, no later than November 30, 2021.

For more information about the position, please contact Carl Sjöberg, Manager Software Development, [email protected] +46 73 050 04 69

The recruitment is for a permanent employment.

We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical.

About Antaros Medical

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We are specialised in cardiorenal & metabolic diseases and oncology.

We combine ground-breaking imaging with profound experience in drug development and a deep knowledge in disease mechanisms. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST. Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. Visa mindre

Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

We value competence and development as well as ideas and creativity. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 90 employees working at our offices in Sweden in Mölndal and Uppsala, as well as a newly established subsidiary in the US, and we are continuously growing and developing.

As a part of our growth journey, we are looking for our next Clinical Project Manager with experience in clinical drug development. You will ideally join our office in Mölndal or Uppsala in Sweden, with flexibility to partly work home-based. The position could possibly be placed internationally home-based in the US or Europe.

As a Clinical Project Manager at Antaros Medical, you will be overall responsible and accountable for project management of the imaging part in clinical trials, from initiation to end of assigned projects. Your responsibility includes to ensure the projects are delivered accordingly with timelines, to the agreed budget, with high quality, and per internal and client’s SOPs, ICH/GCP and other regulation.

Your main responsibilities will be:

- Manage multiple projects ranging in size and complexity, from single to multicenter studies
- Act as a primary contact to the client to ensure smooth operations and communication
- Manage the internal trial team to ensure the right input at the right time from different skills within the company
- Present project information at internal and external meetings
- Risk management responsibility and lessons learned for assigned projects
- Manage the project financials in collaboration with the Finance Department and financial follow-up for assigned projects


Who are we looking for?

We believe that you have demonstrated collaboration skills as well as a team-oriented approach to engage with colleagues and clients. You have the flexibility and the ability to handle multiple tasks and projects to meet deadlines while delivering high-quality work in a dynamic environment.

As a person, we further believe that you are outgoing and enthusiastic, a natural communicator, and can adapt your approach depending on the situation. You work as a team player and apply communicative and interactive skills on different levels within the organization and with external parties and customers.

Requirements:

- University degree in Life Science
- At least 3 years’ experience from working with clinical trials from start to end of projects
- Experience within project management of clinical trials is meritorious
- Strong understanding of ICH-GCP and other relevant regulations and guidelines in relation to clinical trials
- Understanding of the full drug development process
- Excellent written and verbal communication skills in English


Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than November 30th, 2021.

For more information about the position, please contact Neha Mehta, +46 76 111 06 59, or [email protected].

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/) Visa mindre

Are you interested in medical images and image analysis? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A company, where you would contribute and be a part of a collaborative team? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We have currently around 90 employees working at our offices in Sweden in Mölndal and Uppsala, as well as a newly established subsidiary in the US, and we are continuously growing and developing. As a part of our growth journey, we are looking for our next analytical and detail-focused Image Analyst to join our Corelab Team in Uppsala.

As an Image Analyst, you will be responsible for delivering high quality measurements and analyses of the imaging scans from MR and PET investigations, which is a core output from our company. You will work in a team that together analyses and delivers data for the clinical study. Your responsibility also includes quality control of such images and communication with imaging centres on image quality. The job environment is highly focused on research and technical development, and requires collaboration within the internal project team as well as with national and international clients and imaging centres.

Your main responsibilities will be:

- Quality control of the imaging scans and related documentation from the MR and PET investigations in the clinical trials
- Segmentation and analysis of the imaging scans from the MR and PET investigations including documentation
- Compiling results from image analysis and report back to clients according to agreed timelines
- Development, maintenance, and archiving of study documentation


Who are we looking for?

We emphasise personal suitability, and believe that you are a structured and thorough person with attention to details, who strives in an environment where high demands are placed on quality. We further believe that you are a service-oriented person who enjoys collaborating with others, as well as working individually.

We are happy to see that you have an interest in images, image analysis, technology and medicine.

Desired qualifications and skills:

- At least high school grade or equivalent, preferably in natural science. We perceive it as an advantage if you have university- or relevant higher education as biomedical scientist or similar.
- Demonstrated computer proficiency (programming skills are meritorious)
- Good knowledge of spoken and written Swedish and English


Understanding of and/or experience from working with clinical trials is considered an an advantage, including knowledge of ICH-GCP. We further perceive it as beneficial if you have skills and interest in programming.

Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than October 31, 2021. Interviews can take place during the advertisement period.

For more information about the position, please contact Anna Ringheim Cadete, Corelab Manager, at +46 73 233 00 03 or [email protected].

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/) Visa mindre

Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

We value competence and development as well as ideas and creativity. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 90 employees working at our offices in Sweden in Mölndal and Uppsala, as well as a newly established subsidiary in the US, and we are continuously growing and developing.

As a part of our growth journey, we are looking for our next Clinical Project Manager with experience in clinical drug development. You will ideally join our office in Mölndal or Uppsala in Sweden, with flexibility to partly work home-based. The position could possibly be placed internationally home-based in the US or Europe.

As a Clinical Project Manager at Antaros Medical, you will be overall responsible and accountable for project management of the imaging part in clinical trials, from initiation to end of assigned projects. Your responsibility includes to ensure the projects are delivered accordingly with timelines, to the agreed budget, with high quality, and per internal and client’s SOPs, ICH/GCP and other regulation.

Your main responsibilities will be:

- Manage multiple projects ranging in size and complexity, from single to multicenter studies
- Act as a primary contact to the client to ensure smooth operations and communication
- Manage the internal trial team to ensure the right input at the right time from different skills within the company
- Present project information at internal and external meetings
- Risk management responsibility and lessons learned for assigned projects
- Manage the project financials in collaboration with the Finance Department and financial follow-up for assigned projects


Who are we looking for?

We believe that you have demonstrated collaboration skills as well as a team-oriented approach to engage with colleagues and clients. You have the flexibility and the ability to handle multiple tasks and projects to meet deadlines while delivering high-quality work in a dynamic environment.

As a person, we further believe that you are outgoing and enthusiastic, a natural communicator, and can adapt your approach depending on the situation. You work as a team player and apply communicative and interactive skills on different levels within the organization and with external parties and customers.

Requirements:

- University degree in Life Science
- At least 3 years’ experience from working with clinical trials from start to end of projects
- Experience within project management of clinical trials is meritorious
- Strong understanding of ICH-GCP and other relevant regulations and guidelines in relation to clinical trials
- Understanding of the full drug development process
- Excellent written and verbal communication skills in Swedish and English


Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than 31st October, 2021.

For more information about the position, please contact Neha Mehta, +46 76 111 06 59, or [email protected].

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/) Visa mindre

Does software development of image processing and analysis tools catch your eye? How about working in an innovative company within the global Life Science sector where your work contributes to improving drug development of the future? Are you a person who enjoys a dynamic environment and to be part of a growing team with software developers and specialists? If it ticks your boxes, you should continue reading.

At Antaros Medical, we value competence and development as well as ideas and creativity. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 80 employees working at our offices in Sweden in Mölndal and Uppsala, as well as in the US, and we are continuously growing. As a part of our growth journey, we are looking for our next experienced Software Developer for implementation and validation of software used in clinical trials, to join our Uppsala office.

As a Software Developer, you will join a growing team of software developers and specialists in image processing and image analysis. You will further be part of cross-functional project teams in clinical trials, coordinating software development solutions in the project. This includes working with many different roles in the company such as project management and internal end-users of software. You will be responsible for software development of tools for managing and analysing medical images acquired in clinical trials, consisting of MR and PET images.

You will further support with verification and validation of developed as well as acquired software, including requirement management and test protocol creation.

In addition, your work role will include support in method development and medical image processing.

Your main responsibilities will be:

- Development of software tools for medical image management, processing, and analysis.
- Validation of software for analysis of medical imaging data.
- Maintenance and internal support for developed software.


Additional responsibilities could include:

- System owner of applicable computerised systems.

Who are we looking for?

We believe that you have been working with professional software development, preferably with medical images, and including verification and validation, for at least 4 years. You are keen on working both independently as well as in teams with software development of image management and image processing systems.

As a person, you have a logic mindset and analytic ability to solve and conclude issues of different character. You are creative by thinking outside the box and approaching a problem from different angles. We further believe that you have demonstrated collaborative and communicative skills to engage with colleagues and clients, including colleagues with other backgrounds than software development. You have the flexibility and ability to meet deadlines while being thorough and delivering high quality work in a dynamic environment.

Requirements:

- 4+ years’ experience of professional software development, including verification and validation
- B.Sc. degree in relevant field
- Proficiency in Python


It is meritorious if you have previous work experience of GCP/GAMP, as well as software development within a regulated industry, such as medical device development or clinical trials, including experience from medical images of MR and PET. It is further perceived as beneficial if you have studied computer science, engineering physics, applied systems science, and/or software development. Longer experience with software development is meriting.

In addition, we perceive professional knowledge of Matlab, C++, AWS, and requirement management to be of advantage in the work role.

Are you interested?

Great to hear! Please submit your application via this link with a short personal letter (in English) and your CV included, no later than 31st October 2021.

For more information about the position, please contact Carl Sjöberg, Director Image Processing and Software Development, [email protected] +46 73 050 04 69

The recruitment is for a permanent employment.

We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical.

About Antaros Medical

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We are specialised in cardiorenal & metabolic diseases and oncology.

We combine ground-breaking imaging with profound experience in drug development and a deep knowledge in disease mechanisms. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST. Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. Visa mindre

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 team leader till ett av våra hårdvaruteam. Du kommer leda ett team med ingenjörer inom elektronik, mekanik, embedded, optik och testning. Tillsammans utvecklar ni nästa generations system för läkemedel och vaccinframställning. Är du intresserad av att leda andra och samtidigt hjälpa till att designa och förbättra produkter? Då vill vi höra ifrån dig.
Arbetsuppgifter
Leda och koordinera arbetsuppgifter i ett team med ca 10 ingenjörer inom mekanik, elektronik, optik, embedded och testning.
Säkerställa att designen på våra produkter möter våra projektmål för en effektiv överföring till produktion och service.
Stötta teamet i design av våra system. Bidra med kunskap gällande design, lösningar, komponenter, verktyg, metoder och utredningar..
Designa produkter som innehåller robotar, pumpar, ventiler, detektorer och mycket mer.
Utveckla våra agila arbetssätt tillsammans med våra team och andra team leads

Vem är du?
Minst högskoleingenjör med 5 års relevant arbetslivserfarenhet
Stort eget driv och tekniskt intresse med vilja att utvecklas
Erfarenhet av att arbeta med design från utvecklingsfas till produktion, gärna i en agil miljö
Flytande i svenska och engelska, såväl tal som skrift.



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.
Urval och intervjuer sker löpande och sista ansökningsdag är 8e Augusti. För frågor kontakta gärna Thomas Arctaedius, [email protected].
Vill du veta mer? Spana in vår Careers webbsida (https://jobs.danaher.com/global/en/cytiva) , Instagram-kanal (https://www.instagram.com/cytiva/) och LinkedIn-sida (https://www.linkedin.com/company/cytiva/) !
Cytiva är en 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. Visa mindre

About Galderma

Galderma, the world's largest independent global dermatology company, was created in 1981 and is now present in over 100 countries with an extensive product portfolio to treat a range of dermatological conditions. The company partners with health care practitioners around the world to meet the skin health needs of people throughout their lifetime. Galderma is a leader in research and development of scientifically defined and medically proven innovative solutions for the skin. For more information, please visit www.galderma.com.

Job description / Arbetsbeskrivning

The Regulatory Affairs Department at Galderma Uppsala is responsible for all Regulatory aspects of Galderma's aesthetic business at Global level. This includes new product registrations, line extensions and Life Cycle Management of the portfolio of products for both Pharmaceuticals and Medical Device. We manage a broad portfolio of products across almost 90 markets and are expanding our scope with several new innovation projects in our pipeline.

We are now expanding our Medical Device Regulatory Team in Uppsala and looking for a Senior Regulatory Affairs Manager to take on a roll within the team.

Job responsibilities / Ditt uppdrag

About the role
As Senior Regulatory Affairs Manager you will represent Regulatory Affairs as Regulatory Lead in key development and life cycle management projects. You will be responsible for co-ordination and dossier compilation. The role also includes managing Life Cycle Management activities including variations, renewals, labelling changes etc.

Your responsibilities would include:

* Act as Global Regulatory lead within multi-functional project teams, provide support and influence decision-making in order to enable project delivery within defined targets.

* Analyze regulatory requirements and develop regulatory strategies world-wide, including active communication with local Regulatory Authorities and Galderma affiliates.

* Deliver high quality regulatory documentation for all activities either Development projects or Life Cycle Management Projects.

* Represent Regulatory Affairs in internal and external audits.
* Geographical Expansion of the portfolio

* License maintenance
* Surveillance of regulatory requirements - at Global level

Minimum requirements/ Är du den vi söker?

About you

* You hold a university degree in a life science area such as Pharmaceutical Science or similar.
* You also have several years' experience of Regulatory Affairs within the Pharmaceutical or Medical Device industry, or from an Authority (Health authority, Notified Body or similar) perspective.
* You have experience of compiling and reviewing documents/reports according to Global regulatory guidelines.
* You are open-minded and willing to adapt to changes and enjoy working with others in a collaborative way, also across several cultures
* You are self-driven, flexible, methodical, with the ability to structure work and manage multiple requests while maintaining timelines
* You possess good communication skills and fluency in Swedish and English, both verbal and written. Strong writing, reading and reviewing skills are necessary.



Other important information/ Frågor och ansökan

What we offer in return
As Galderma's Global Center of Excellence for Aesthetics we have in Uppsala a unique edge as we have on our site the whole product chain from research and development to production and marketing. Here our nearly 450 employees work on our world leading brands such as Restylane, Azzalure and Sculptra.

We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10 minute bike ride from Uppsala Central Station.



Your application
We welcome your application (CV and letter) via our company website

https://www.galderma.com/job-search or by clicking "Apply Now" below.

Apply as soon as possible though no later than 13th April. The selection process is ongoing.



Should you have questions about this opportunity you are welcome to contact

Sinéad Breen, Global Head of Regulatory Affairs at +46 768981230 Visa mindre

About the role

Bio-Works is looking to strengthen its Quality Assurance team with a director-level role tasked with defining and promoting a quality mindset across the entire company. The QA Director is responsible for managing all QA functions, working with cross-departmental leadership to deliver high-quality products on schedule.

Responsibilities

- Assures quality products and processes by establishing and enforcing quality standards and testing materials and products per ISO 9001:2015.
- Develop the QA function according to Bio-Works' strategic plan
- Act independently of Bio-Works management in handling QMS resources and activities
- Create product quality documentation system by writing and updating quality assurance procedures.
- Maintain product quality by enforcing quality assurance policies and procedures and government requirements.
- Collaborate with other members of management to develop new product and engineering designs and manufacturing and training methods.
- Prepare product and process quality reports by collecting, analyzing, and summarizing information and trends.
- Complete quality assurance operational requirements by scheduling and assigning employees and following up on work results.
- Develop a quality assurance staff by recruiting, selecting, orienting, and training employees.
- Manage quality assurance staff job results by coaching, counseling, and disciplining employees.
- Ensure quality by planning, monitoring, and appraising job results.
- Maintain professional and technical knowledge by attending educational workshops, reviewing professional publications, establishing personal networks, and participating in professional societies.
- Achieve financial objectives by preparing the quality assurance budget, scheduling expenditures, analyzing variances, and initiating corrective actions.
- Contribute to team effort by accomplishing related results as needed.


Requirements (skills)

- BA or BS in appropriate discipline
- Five to 10 years’ experience as QA manager or director in ISO 9001:2015 company
- Working knowledge of quality system requirements
- Experience with MS Word, Excel, Project Management and Analytics software
- Strong communication, negotiation, and management skills.
- Business fluency in English and Swedish are required.
- Experience with LEAN / KANBAN / Six Sigma is a plus.


Requirements (personality)

- Strong leadership skills both in terms of self-leadership and leading teams
- A proactive risk-based attitude focused on identifying problems and solutions.
- A collaborative mindset
- A precise and analytic mindset to identify and focus on issues and risks.




Do you have a question?

For any questions, you are warmly welcomed to contact Jonathan Royce at [email protected]. Visa mindre

Fresenius Kabi har en global forsknings- och utvecklingsorganisation som ansvarar för produktutveckling och strategisk marknadsföring inom företagets olika verksamhetsområden. I Sverige finns enheten för Forskning och Utveckling inom Parenteral nutrition, (PN), som är lokaliserad i anslutning till produktionsanläggningen i Uppsala. Verksamheten omfattar farmaceutisk och analytisk utveckling och dokumentation av nya PN produkter, och arbetet bedrivs i projektform tillsammans med strategisk marknad, preklinisk och klinisk utveckling, som är lokaliserad till Tyskland, och registreringsavdelningen, som också finns i Uppsala. En mycket viktig del är samverkan med produktionsenheterna, såväl i Uppsala som på andra platser, för uppskalning och tillverkning under utvecklingsprocessens gång.

Fresenius Kabi i Uppsala söker en Manager Technical Development & Maintenance för att leda en nyligen skapad supportgrupp med ansvarsområdet teknisk utveckling och underhåll inom avdelningen Innovation & Development (I&D) Center Sweden. I&D Center Sweden utvecklar nya resp förbättrar befintliga produkter inom parenteral nutrition. Avdelningen består av fyra grupper som sammanlagt omfattar ett trettiotal medarbetare. Utvecklingsarbete bedrivs i projektform samt följer GMP regler och andra myndighetskrav. Som Manager Technical Development & Maintenance leder du en grupp om tre medarbetare som ansvarar för förebyggande underhåll av befintlig utrustning, inköp av ny utrustning, underhåll av lokaler och hantering av stabilitetsstudier. Även dataintegritetsfunktionen ligger inom gruppens ansvar. Därutöver arbetar gruppen med teknisk utvärdering av nya tekniker (tillverkning/mät/analys). Du rapporterar till Vice President I&DC; Sweden och ingår i avdelningens ledningsgrupp.

 

Arbetsuppgifter inom tjänsten:

Leda gruppen Technical Development & Maintenance och planlägga gruppens arbete.
Sätta mål för gruppen och dess medarbetare utifrån avdelningens övergripande mål och följa upp på gruppens KPI:er.
Inspirera, motivera och kompetensutveckla gruppens medarbetare.
Planera och följa upp budgeten för gruppens ansvarsområde samt för avdelningens capex projekt.
Deltaga i avdelningens ledningsgrupp.
Ansvara för att arbetsmiljölagar och GMP regler följs.
Planera, utföra och avrapportera underhållsaktiviteter för avdelningens utrustning, instrument och datoriserade system.
Underhålla avdelningens instrumentregister.
Delta i kvalitetsarbetet inom funktionen.
Upprätta och granska styrande och redovisande kvalitetsdokument inom ansvarsområdet.
Genomföra utvärdering och inköp av utrustning.
Initiera och deltaga i avdelningens förbättringsarbete.
 

Kvalifikationer:

Vi söker dig med akademisk utbildning inom kemi/kemiteknik, farmaci eller motsvarande. Du har minst fem års erfarenhet från läkemedelsindustrin eller annan relevant industri och är förtrogen med GMP-regelverk. Vi ser gärna att du har en viss ledarskapserfarenhet, t ex som linjechef eller projektledare. Kunskap inom dataintegritet/datoriserade system är en merit. Du måste ha goda kunskaper i både svenska och engelska i både tal och skrift.

 

Personliga egenskaper och kompetenser som vi värderar är:

Mycket god kommunikations- och samarbetsförmåga, då tjänsten kräver samverkan och samarbeten med andra grupper både i Sverige men även internationellt.
God planerings- och problemlösningsförmåga samt stort intresse av tekniska frågeställningar.
Du är kvalitetsmedveten, resultatorienterad, sätter ambitiösa mål och levererar i tid.
Som chef är du en förebild och motiverar dina medarbetare. Du är entusiastisk och positiv även i tuffa situationer.
Du söker nya perspektiv och idéer för att stimulera innovation och förändring.
Prioriteringsförmåga.
 

Uppdragsgivare: Fresenius Kabi

Ort: Uppsala

Omfattning: Heltid tillsvidare. Anställningen inleds med 6 månaders tidsbegränsad visstidsanställning (motsvarande provanställning).

Sista ansökningsdag: 31 mars 2021. OBS, utvärdering och intervjuer sker löpande. Tjänsten kan därför bli tillsatt innan sista ansökningsdatum.

 

För information: För frågor, kontakta ansvarig chef Britta Siekmann 018-644 389. För oss är det viktigt att all kompetens på arbetsmarknaden tillvaratas. Vi välkomnar alla sökande och eftersträvar mångfald. Fackliga kontaktpersoner är Frank Glackin för Unionen, 018-644 773 och Linda Holm för SACO, 018-644 195. Visa mindre

Om företaget

Rolba Svenska AB i Hedesunda grundades 1962, verksamheten omfattar alla steg från idé till leverans av färdig produkt. Företaget omsätter ca: 190 mkr och är idag 55st anställda. Vår personal kännetecknas av bred kompetens med ett personligt engagemang. Våra marknadsandelar ökar stadigt i Sverige, Finland, Norge, Danmark samt England och vi är en ledande tillverkare av högkvalitativ utrustning för slamsugning, högtrycksspolning monterade på lastbilschassier. Vår kundkrets finns inom företag och kommuner. Läs mer på www.rolba.se

Dina arbetsuppgifter

Vi söker en konstruktionschef

Rolba har en stor produktionsanläggning i Hedesunda som idag är hjärtat av verksamheten med ett huvudkontor där ledning, produktutveckling och produktion finns under samma tak. Rolba ansvarar för hela operativa Supply Chain, från R&D till After Sales. Rolba präglas av ett intensivt och mångsidigt förbättringsarbete för att säkra företagets strävan till fortsatt tillväxt och att etablera sig som en marknadsledande koncern. Kvalitet, Service och Effektivitet är några av våra viktigaste framgångsfaktorer.

Konstruktionsavdelningen utgör en viktig komponent i vår framgång. Avdelningen ansvarar för att koncernen har en konkurrenskraftig produktportfölj samt driver ett antal stora och små projekt på en relativt högteknisk nivå. Vårt team arbetar ständigt för att säkerställa att tillverkningsprocessen når de kort- och långsiktiga mål vad det gäller kostnadseffektivitet, produktivitet, leveransprecision och kvalitet.

Arbetsuppgifter

Att arbeta hos oss innebär att arbeta i ett högt tempo i en kreativ och spännande miljö, ofta med flera parallella uppdrag. Tillsammans med duktiga medarbetare kommer du att direkt påverka våra produkter och företagets förmåga att nå sina mål. Du kommer till en flexibel organisation där du har stora möjligheter att påverka ditt arbete. Som konstruktionschef i på Rolba ingår du i företagets ledningsgrupp.

Om du dessutom vill få utlopp för din kreativitet och ”triggas” av att se ditt avdelningsarbete utvecklas från tanke till färdig produkt kommer du att trivas hos oss. Utveckling, Modularisering, Design samt löpande ritningsarbete är vanliga uppgifter på avdelningen där du blir en viktig del i att leda och fördela arbetet på bästa sätt för att nå uppsatta mål för avdelningen och företaget. I tjänsten ingår också fullt personalansvar för din avdelning bestående av 5 personer med kompetens inom hydraulik, el, 3D CAD, mekanisk konstruktion samt högtycksspolning och vakuumteknik.

Din profil

Vi söker dig som har ett genuint intresse av ledarskap!

För att lyckas i din roll är du en person som har viljan att ta ett stort ansvar. Du trivs med att leda och driva ditt team mot uppsatta mål och har stort fokus på att uppnå resultat. Att samarbeta med olika avdelningar är en självklarhet för dig och du finner stor glädje i att engagera och entusiasmera dina kollegor.

Din kompetens är också viktigt för oss.
För att bli framgångsrik i din roll som konstruktionschef på Rolba ser vi att du har erfarenhet eller utbildning inom arbetsledning, personalansvar och projektledning samt besitter en god teknisk förståelse. Vi ser det som meriterande om du har erfarenhet av att jobba nära kunder, besitter ett genuint teknikintresse och har praktiskt erfarenhet av tillverkning. Har du dessutom erfarenhet från fordonsindustrin, design och konstruktion, är utbildad Högskole- eller civilingenjör inom maskinkonstruktion eller motsvarande är det mycket meriterande.

Ansökan

I den här rekryteringen samarbetar vi med Clockwork Rekrytering & bemanning. För mer information om tjänsten är du varmt välkommen att kontakta rekryteringskonsult Poria Shademani på tel. 0733512720 [email protected]. Vi arbetar med rekryteringsprocessen löpande, så ansök så snart som möjligt via www.clockworkpersonal.se Visa mindre

IAR Systems is a knowledge-intensive and value-driven truly global company at the top of our industry. We have been providing world-leading software for building embedded applications for more than 35 years, and today over 150,000 developers are using our software. We supply the tools and services that make embedded systems development fast, efficient, and reliable, enabling our customers worldwide to deliver better products to their markets faster.
About the role
As an Engineering Manager at IAR Systems, you will support the success of a team of 10-20 skilled and experienced software engineers, where you communicate expectations, initiatives, and goals. You will be part of the engineering management team and actively contribute to the continuous development of the department. In this role, you will also have close contact and collaborate with stake holders across various domains, such as project leaders and product managers.
You will be responsible for budgeting, and managing employees through the full employee journey of hiring, mentoring, performance and salary reviews, and exits. You will be responsible for your team’s outcomes, and for coaching your team to continuously deliver value to the stake holders and working towards the company’s goals.
You will report to the Director of Engineering and will be located in Uppsala.
Your qualifications and experience
You have some previous management experience with the know-how and ability to do what is needed to plan and uphold project plans, and deliver accordingly. As a manager of experienced engineers, a solid background in software engineering is a must so that you’re able to challenge and coach your team members in a collaborative, delivery-focused environment. Experience to advocate and advance modern software engineering practices is a prerequisite for the role. You are fluent in Swedish and English in both writing and speaking.
Communication is your most important tool. You will build and inspire your team by enabling a creative and challenging atmosphere. To be successful in this role, we believe you will bring a positive attitude, have the ability to deliver and receive constructive feedback, and gain the trust of your team.
Your application will receive extra credit if you have experience with DevOps, Cloud platforms, and Linux. In addition, it is a bonus if you have domain knowledge in any of the areas of microprocessor architecture, embedded systems, hardware-oriented development, or software development tools, such as compilers, debuggers, IDE, etc.
What are we offering?
You will be part of a multi-cultural and global business in a fast growing industry, an organization where every co-worker’s individual role is very important in the big picture. We are welcoming, open to new ideas, and take pride in our achievements. We offer you the opportunity to work in a curious, knowledge-sharing environment with a strong team spirit, where we will support you to grow both professionally and as an individual. We are problem-solvers and take on new challenges with excitement and energy. This is why we place great emphasis on your personal qualities and their alignment with our values.
Are you the person we are looking for? Please send us your application with cover letter and resume/CV today, and indicate “Engineering Manager” in the subject line. Selection and interviews will take place on a continuous basis and the post may be filled before the closing date, so please apply as soon as possible.
Questions? If you have any questions, please turn to Susanne Dahlén, Director of Engineering, at [email protected]
Applications are to be sent to [email protected] Visa mindre

Galderma is the world's largest independent global dermatology company.  Our Global Center of Excellence for Aesthetics is located in Uppsala, Sweden. Our Global Project Management department manages product development projects for medical device and pharmaceutical products within the Aesthetics area.

 

About the role

As Senior Project Manager, will you provide day-to-day project management to global drug/medical device development project teams in the Aesthetics Global Business Unit. In close collaboration with other functions within the company, you will drive the Aesthetics innovation pipeline progression to ensure timely supply of quality products to our customers and contribute to Galderma’s short- and long-term growth.

 

As Senior Project Manager, you will:
* Manage global cross-functional teams of professionals responsible for product development from early stage until launch
* Be accountable for project objectives, deliverables, timeline and budget
* Manage project decision making
* Be responsible for developing and communicating strategies, goals and long-term vision for projects
* Implement and organize actions to improve team motivation and shared understanding
* Ensure and facilitate cross-functional collaboration
* Assess project risks with the project team, propose and follow-up mitigation and contingency plans 
* Ensure appropriate reporting of project progression inside and outside the team
* Issue the project core documentation

 

About you

We believe that you have a university degree within science, engineering or business. You have at least 5 years of experience as project manager, with specific experience from the pharmaceutical industry including clinical development. You are used to working in an international environment.

 

We think that you have the following skills and competences:
* Excellent skills in project management tools and practices
* Excellent communication skills, both oral and written communication
* Good team leadership skills
* Good financial knowledge
* An analytical and strategic mindset
* Experience in change management

We also believe that you are courageous, ambitious and goal-oriented. You know how to influence others and you have integrity and an open mind.

What we offer in return

As Galderma’s Global Center of Excellence for Aesthetics, we have in Uppsala a unique edge as we have on our site the whole product chain from development to production and marketing. Here our nearly 450 employees work on our world leading brands such as Restylane, Azzalure and Sculptra.

We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10 minute bike ride from Uppsala Central Station.

Your application

We welcome your application (resume and cover letter) via our company website www.galderma.com/job-search. You will be able to create a personal account and upload your application documents. Apply as soon as possible though no later than January 10, 2020. The selection process is ongoing.

Should you have questions about this opportunity you are welcome to contact Malin Johansson, Global Head of Project Management, on +46 73 387 1498.

We look forward to receiving your application!

About Galderma

Galderma, the world's largest independent global dermatology company, was created in 1981 and is now present in over 100 countries with an extensive product portfolio to treat a range of dermatological conditions. The company partners with health care practitioners around the world to meet the skin health needs of people throughout their lifetime. Galderma is a leader in research and development of scientifically defined and medically proven innovative solutions for the skin. For more information, please visit www.galderma.com. Visa mindre

Vill du arbeta på ett företag i framkant med modern teknologi? Bolaget driver samarbeten med stora dynamiska globala bolag samt levererar till kunder över hela världen. De globala bolagen är bl a verksamma inom diagnostik, halvledarindustri och avancerade optiska mätningar.

Huvudkontor samt anläggning för utveckling och produktion finns i Upplands län.





Om uppdraget

Denna roll är en kombinerad roll som ledare för avdelningen Design Engineering och samtidig Senior projektledare för ett eller flera av våra absolut viktigaste produkt- och industrialiseringsprojekt.

Bolaget har som plan att expandera och som en del av detta kommer utvecklingsavdelningen att bestå av två olika delar, en innovation/R&D del och en del som ansvarar för utveckling, färdigställande av produkter samt att driva kundanpassade projekt.

Tjänsten vi erbjuder är i ett teknikområde som innehåller ett stort mått av nytänkande och där det inte alltid finns färdiga lösningar för uppgifterna. Här har du en unik möjlighet att själv kunna ta fram idéer kring koncept och att initialt själv vara med i det praktiska framtagandet av produkter. Vi arbetar i en spännande internationell miljö där resor förekommer. Vår strävan är att alltid vara den som snabbast levererar en fungerande lösning till kunden.

Är du den vi söker?

Vi söker dig med en Civilingenjörsexamen, gärna inom maskin, material eller teknisk fysik. Du har god kunskap och förståelse inom elektronik och mjukvara, gedigen erfarenhet av produktutveckling samt projektledning. Vi ser att du har erfarenhet av att implementera utvecklings- och projektlednings-processer. Du har erfarenhet av att etablera en effektiv organisation som både kan driva egna produktprojekt, kundanpassade projekt samt stödja Innovation/R&D avdelningen med vissa utvecklingsresurser.

Vi söker dig som har erfarenhet kring att arbeta med globala bolag. Du har någon form av internationell erfarenhet, helst via arbete mot internationella kunder men gärna även genom arbete i andra länder alternativt i en internationell organisation. Det är meriterande med erfarenhet kring både utveckling av högvolymkomponenter och sub-system, gärna inom olika applikationsområden. Du har gärna någon typ av entreprenörserfarenhet, antingen genom arbete i en startup eller genom deltagande i etablering av ny verksamhet.

Personliga egenskaper

Dina drivkrafter och egenskaper innebär att du kan implementera en kultur med kundfokus, snabbhet, flexibilitet och öppenhet, en organisation där medarbetarna mår bra och är beredda att delegera ansvar men också är beredda att ta ansvar. Du tycker det är viktigt att ha roligt på jobbet i kombination med att du levererar ett stort värde.

Låter det intressant?

Låter detta intressant är du välkommen att kontakta Amanda Norstedt, [email protected], tel. 070-236 36 99 för mer information om tjänsten. Visa mindre

Do you want to be part of the largest independent company focused on dermatology? Do you want to be a key driver for the Galderma Aesthetic Global Medical Affairs Strategy? Then this can be the role for you!
The Global Medical Affairs department in Uppsala, Sweden, is responsible for providing specialist medical and scientific support to Healthcare Professionals (HCPs) and Galderma staff. We are directly involved in the strategic discussions and decision-making regarding new data generation, publications and other forums for sharing of information about our aesthetic products or best practices. Our work is focused on four areas: medical education and training, publications, clinical studies (Phase IV and IITs), pipeline and global medical affairs strategy.

About the role

As Head of Global Medical and Scientific Experts, you will lead the medical and scientific strategy of the Medical Affairs department for the aesthetics business unit (GBU). Reporting to the Global Head of Medical Affairs, you will be the manager for a team of three Medical Science Advisors. In addition and as a senior resource, you will provide medical insight and support of the Aesthetics GBU activities, both internal and external. The role is located in Uppsala, Sweden and can require about 25% of travel.

As Head of Global Medical and Scientific Experts, your main responsibilities will include:

 
* serving as the key medical resource and lead for the Medical Science Advisors, members of the Phase IV clinical team, and the study strategy and publication team
* serving as the lead for management of Investigator Initiated Studies (IISs)
* liaising closely cross functionally to ensure strong strategic support
* performing review and presentation of clinical data to support publications, claims and other medical affairs activities
* reviewing promotional material
* key Medical Affairs interface with the Safety, Regulatory, Clinical Development and Quality teams
* managing resources and priorities for your team

 

About you

* You have a PhD or MD with a strong preclinical background
* You are fluent in English (written and oral)
* Minimum of 7 years in a global pharmaceutical and/or medical device company in Medical Affairs and Clinical Development
* Demonstrated experience working cross-functionally and building alignment among stakeholders
* Demonstrated experience and working knowledge of international regulations and GCP of medical device and/ or pharmaceuticals
* Demonstrated experience in developing protocols, and conducting phase IV studies; experience in Medical Affairs study strategy
* Demonstrated experience in critically reviewing and analyzing scientific data, and have demonstrated ability to outline and write scientific papers and compile regulatory and technical documents
* Prior leadership experience of guiding teams is preferred

What we offer

As Galderma’s Global Center of Excellence for Aesthetics, we have in Uppsala a unique edge as we have on our site the whole product chain from early development to production and marketing. Here our 450 employees work on our world leading brands such as Restylane®, Azzalure® and Sculptra®.

We are offering you the opportunity to work in a fast growing and international environment, where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala, only a 10-minute bike ride from Uppsala central station.

 

Your application

We welcome your application in English (CV and letter) via our company website www.galderma.com/job-search. Apply as soon as possible though no later than January 15, 2020. The selection process is ongoing. We look forward to reading your application!

Should you have questions about this opportunity you are welcome to contact the HR department on [email protected]

We wish to inform you that Galderma can conduct pre-employment security checks for specific positions or activities. This security screening is performed by an external supplier after approval from applicants.

About Galderma

Galderma, the world's largest independent global dermatology company, was created in 1981 and is now present in over 100 countries with an extensive product portfolio to treat a range of dermatological conditions. The company partners with health care practitioners around the world to meet the skin health needs of people throughout their lifetime. Galderma is a leader in research and development of scientifically defined and medically proven innovative solutions for the skin. For more information, please visit www.galderma.com. Visa mindre

Kvalitetschef
Are you interested in making an impact in the area of radiation therapy and help new products reach the market? Do you want to help patients around the world to get more efficient radiation therapy? C-RAD is looking for their next Director with assignments within quality control, quality assurance and regulatory affairs.



C-RAD works within the field of radiation therapy and are trying to improve among other things real time monitoring of radiation therapy.



Job description

You will implement and maintain Quality Systems for C-Rad global quality and regulatory systems in compliance with US Food and Drug Administration, ICH and international requirements, and will lead the strategic and operational aspects of C-Rad’s quality and regulatory program. You are responsible for the Quality Control and Quality Assurance functions and ensure compliance to corporate policies, US FDA, other applicable federal/state agency and international requirements, as appropriate. You also lead the preparation and submission of regulatory documents in the US and other countries for approval at various stages of the submission process. You will be the contact point towards the FDA, EU and other regulatory agencies.



Other common tasks will be:

- Conducting internal and external audits.

- Manage supplier quality and contract manufacturing quality.

- You will be the global quality representative within the company.

- Provide regulatory training and foster a corporate commitment to quality.



Qualifications

For this role we see a person who has worked within the field of medical or biological devices. You probably have an bachelor’s degree in engineering, science or other relevant field. Have you also had experience with the FDA and been the lead auditor then this job will suit you. In this role we give you the opportunity to work in a wide range of tasks from implementing a quality system to training the employees and assure quality compliance. As a person we see this employee as an:



- Collaborative person that puts the companies goals first.

- Ability to engage colleagues and keep a positive attitude

- Listen attentively to colleagues and other collaboration partners.



There will be travels less than 20 % of the time. It is important for us to see that all of the competencies in the market. We welcome all candidates.



Application: Please apply before 2019-04-24. In this recruitment selection will take place continuously. Please send in your application today!



Contact information: In this recruitment C-RAD has decided to collaborate with Dfind Science & Engineering. Please contact Jenny Davidsson [email protected] for any questions concerning this position. Visa mindre

Do you want to be part of a business that contributes to human health and well-being? Do you want to work as a Business Development & Alliance Manager in a global organization that is in an expansive phase? Then this can be the role for you!

 

The Business Development Department in Uppsala is responsible for driving and executing business development and alliance activities for our Aesthetic global unit.

 

About the role
Reporting to the Global Head of Business Development, you will focus on managing existing strategic alliances and execute business development activities according to the company priorities and strategic plan.

 

As Business Development & Alliance Manager you will:
* Be the key point of contact for our strategic partners throughout the world
* Manage all aspects of alliances (business reviews, communication, coordination of resources, definition of governance, organization of meetings etc.)
* Manage licensing-in and licensing-out of products, technologies and related materials.
* Manage due diligence processes in coordination with other key departments
* Develop financial models together with finance partner
* Prepare all documents linked to relevant projects (business plan, presentation, secret note etc.)
* Identify and explore new business models and business opportunities to grow our business
* Research market conditions and developments including attendance of key congresses & meetings

 

To be successful in this role you will need to understand and effectively engage a wide range of internal and external functional areas including Legal, Finance, Development, Medical and Regulatory Affairs, Marketing and Project Management.

You are able to travel up to 30% including internationally.

 

About you

We believe that you have the following background:
* University degree in business administration or science.
* +15 years of experience gained in  management roles:
- Commercial positions with international exposure
- Business Development and/or Alliance Management
* Solid experience in and understanding of the pharmaceutical/device industry (aesthetics field preferred)

 

We also believe that you bring the following skills and competences:
* Very good business acumen and financial & negotiation skills
* Advanced Project management skills: you can work both on a strategic level and manage specific operations in a complex context
* Strong collaboration skills across functions and cultures and ability to manage stakeholders
* An analytical and strategic mindset
* Understand customer focus and brand focus
* Strong verbal and written communication and presentation skills in English

 

What we offer in return
As Galderma’s Global Center of Excellence for Aesthetics we have in Uppsala a unique edge as we have on our site the whole product chain from research and development to production and marketing. Here our nearly 450 employees work on our world leading brands such as Restylane, Azzalure and Sculptra.

 

We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10 minute bike ride from Uppsala Central Station.

 

Your application
We welcome your application (CV and letter in English) via our company website https://www.nestleskinhealth.com/job-search. Apply as soon as possible though no later than April 10, 2019. The selection process is ongoing.

Should you have questions about this opportunity you are welcome to contact Daniel de Boer, Global Head of Business Development, on [email protected].

 

We inform candidates that the company may perform a background control as part of the final recruitment step.

 

About the company
Galderma is a global leader in medical solutions for the skin, hair and nails, wholly-owned by Nestlé Skin Health, a subsidiary of Nestlé. The company has been developing its extensive range of medically-proven solutions since its creation in 1981. It exclusively partners with healthcare professionals to target a variety of dermatological conditions and skin needs.

Headquartered in Lausanne, Switzerland, Galderma has more than 5,500 employees and 35 affiliates around the world. Its products are distributed in over 100 countries. Its development centers and manufacturing facilities are dedicated to providing a wide range of innovative and science-based medical solutions to meet the highest standards of safety and efficacy. Visa mindre