Manufacturing Quality Engineer

Be part of something altogether life-changing!

Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.

Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.

The Manufacturing Quality Engineer for Cytiva is responsible to provide technical support to improve product quality.  This position will focus on product quality through data analysis and issue resolution.  This person will be responsible for driving the non-conforming material process and root cause investigation through coordination with Contract Manufacturing Program Managers, Lifecycle Management Team, Quality Specialists and Supplier Quality Engineers.

This position is part of the Standard and Custom Operations Team (SCO) located in Uppsala and will be an onsite role. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.

What you will do:

• Ownership of the Deviation handling process

• Lead analysis of supplier non-conformance data and maintenance of records in Enovia defect management system

• Lead analysis of supplier deviations and quality follow up with suppliers

• Interface with Supplier Quality and Global Sourcing on supplier related defects

• Conduct root cause analysis on product quality issues, identify trends, and collaborate with SQEs, Lifecycle Management Team and Global Sourcing for resolution, send improvements suggestions to CCB.

• Responsibility of non-conforming material inventory

• Support Case Management

Who you are:

• Technical knowledge of manufacturing processes

• Quality focus

• Strong communication skills, verbal and written

• Experience from production or design of work of products for the Biopharmaceutical industry

• Bachelor Degree in Mechanical Engineering or equivalent.

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

• Quality management, CAPA

• ISO9001:2015

Application
We review applications on an ongoing basis and encourage you to submit yours as soon as possible.
 

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

Danaher

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.