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Help us improve access to life-changing therapies that can transform human health

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

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

We are looking for a SENIOR PROJECT MANAGER NPI, QUALIFICATION SERVICES to work with our specialist QUALIFICATION SERVICES team of approximately 50 employees across the world. Do you have an interest for COMMISSIONING/QUALIFICATION and PROJECT MANAGEMENT?

Then we would love to hear from you.

What you'll do

As a result of an increasing demand of commissioning and qualification products we need to streamline our processes for developing new documentation. Advanced communication skills will be critical for success. You will work across team and stakeholders across the globe, but majority is Europe and US based. If you like to work in a dynamic environment where you have the possibility to influence processes and help our customers to meet their regulatory demands you might be the right person for this role. Preferred location is Uppsala, Sweden but other locations may be considered.

  • Planning and securing timelines, goals and resources for qualification documentation that is needed in new product projects

  • When needed identify technical resources from qualification service department

  • Communicate current state to senior management to secure deliverables

  • Develop and maintain processes and ensure smooth daily interactions with other Qualification Services teams as well as the wider business.

  • Responsible for ensuring that the current New Product Introduction (NPI) process for qualification documentation is followed and that future improvements are documented and implemented as appropriate

  • Facilitate team communication and best practice sharing

Who you are

  • Education: Master degree in Science, Engineering or related area or equivalent

  • 10 years’ experience working with 21 CFR Part 11, GAMP 5, Annex 11, GxP and other regulatory standards in Healthcare.

  • 5 years’ experience of working in projects and demonstrated capability of cross-functional and cross-site interactions

  • Ability to drive project plans to completion.

  • Fluent in English, advantage to speak Swedish

  • Excellent communication and team-work skills.

  • Proficiency in PC computer skills and in Microsoft Office Suite products.

  • Willingness to travel.

  • EU or UK work permit.


  • Experience of instrument development

Who we are

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

Our business is growing quickly and we hire across the board. Interview and selection will happen continuously and an opening can be filled before last day of application, 19th February. For questions about the role, please contact hiring manager Anneli Karlsson, anneli.karlsson@cytiva.com.

Want to know more? Experience life at Cytiva on our Careers website (https://jobs.danaher.com/global/en/cytiva) , Instagram channel (https://www.instagram.com/cytiva/) and LinkedIn page (https://www.linkedin.com/company/cytiva/) !

Cytiva is global life sciences leader with over 7000 associates across 40 countries who are dedicated to our mission to advance and accelerate therapeutics. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients.

Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world.

Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here (http://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf) .