Be part of something altogether life-changing!
This is a consulting assignment until 31/3 2027, with the possibility of extension.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
About the assignment
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics. The Manufacturing Quality Engineer at Cytiva provides technical support to improve product quality, with a focus on data analysis, issue resolution, and continuous improvement. This role is responsible for driving the non-conforming material process and supporting root cause investigations by coordinating with Production Engineers, Quality Specialists, Supplier Quality Engineers, affected project teams, and manufacturing suppliers.
This position is part of the Custom Engineering Manufacturing team and located in Uppsala. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
Who should apply for this job?
Essential qualifications
Ownership of the Deviation handling process • Coordinate and document manufacturing quality issues to ensure clear ownership, effective follow-up, and timely resolution. • Coordinate resources to support problem-solving and rework activities in ongoing production for manufacturing quality-related issues. • Lead analysis of supplier deviations and quality follow