Quality Assurance Engineer (m/f/d) (Frankfurt)

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 Quality Assurance Engineer (m/f/d) for Cytiva is responsible for maintaining and improving the Quality Management System by ensuring Cytiva, Customer, and Regulatory requirements are being met through project execution and delivery of product.

This position reports to the Site Quality Manager and is part of the Custom Engineering Quality Assurance department located in Dreieich and will be an on-site role.

What you will do:

• Own and execute the product release process for Custom Engineering Dreieich products, ensuring compliance with QMS, regulatory, and customer requirements.

• Own, maintain, and harmonize Custom Engineering SOPs within the global QMS. Coordinate cross‑functional reviews, change control activities, and related training to ensure global implementation and compliance.

• Manage customer complaints, including timely assessment, documentation, response, and trend analysis.

• Manage Deviations and CAPAs in QMS, ensuring effective root cause analysis, implementation of corrective actions, and timely closure.

Who you are:

• Bachelor’s degree in engineering or science discipline.

• Minimum 2-3 years of experience in Quality role, preferably in the Life Sciences industry.

• Good knowledge of using MS Office tools such as MS Excel to perform analytics and data management.

• High attention to detail, good coordination skills, and ability to work cross‑functionally with global QA & Engineering teams.

• Ability to communicate effectively in both German and English (written and spoken).

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

• Knowledge and awareness of the methods and techniques of Quality Control in the manufacturing industry.

• Technical knowledge of systems/devices used in the biopharma field.

• ISO 9001.

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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.

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