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 and Regulatory Support Manager for Cytiva is responsible for supporting the Business and Customers in a global environment by providing quality documents and regulatory support in response to customers' requests for quality, regulatory and technical-related information as it pertains to Bioprocess single use and filtration products.

This position is part of the Regulatory Support Team located in Krakow, Poland and will be onsite. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.

What you’ll do:

Support the Business and Customers in a global environment by providing quality documents and regulatory support in response to customers' requests for quality, regulatory and technical-related information as it pertains to Bioprocess filtration products.

Identify and lead cross functional activities, including creating/updating internal and external documentation to align with industry developments and enhanced customer expectations. Function as the regulatory support expert and discussion partner to R&D, QA, Product Management and other functions, and facilitate risk-based decisions.

Prepare, update and review regulatory support documentation, certificates and other regulatory related documentation for new and existing products.

Respond efficiently and promptly to customers' regulatory based questions and requests, which will include investigations, preparations and delivery of statements and documentation, use of internal and external databases.

Who you are:

Bachelor of Science degree in Biochemistry/Chemistry or related field.

Five or more years of experience in GMP, quality, product management or a related field.

Understanding of quality and regulatory requirements in the Bioprocess industry.

Driven with experience leading cross-functional activities across global teams.

Strong written and verbal communication skills, fluent in English.

It would be a plus if you also possess previous experience/knowledge of

Biopharmaceutical/Bioprocess single use/filtration products and techniques.

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.

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