QA Batch Release Officer

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 QA Batch Release Officer for Cytiva is mainly responsible for the batch record review and final product release and certification. Another part of the job is related to the maintenance and guiding of non-conformance/rework actions and the support of other routine Quality Assurance tasks.

This position is part of the Quality Assurance department located in Medemblik, the Netherlands, and will be on-site. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.

In this role, you will have the opportunity to:

• Review batch documentation records to ensure goods are being released in compliance with the current specifications and internal procedures in a timely and thorough manner
• Certify finished goods for release to customer
• Review customer facing documents to assure GMP compliance

The essential requirements of the job include:

• Junior Bachelor’s degree/MBO in a scientific field, preferable in Life Sciences (bio, biomedical, chemical, pharma) or similar through experience
• 1-3 years of experience in a quality and/or production environment
• Team player with speak up mentality, good communication skills and attention to detail

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

• GMP Requirements, including Good Documentation Practices
• Non-Conformance process / QMS (e.g. ISO 9001)

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.