About the Role

In this role, you will have the opportunity to join our winning team. 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.

Responsibilities

• Manage GSP-related affairs for Cytiva medical devices
• Support the line manager in delivering successful localization projects from a quality perspective in China
• Lead or contribute to post-market QA activities and internal/external audits, with a focus on driving continuous improvements such as timely delivery of CAPAs and maintaining the QMS
• Provide and review Quality Agreements (QAA) for commercial teams and customers in a timely manner
• Communicate with the Global Regulatory Affairs team to support local customers on CCN-related and Hazardous Chemicals issues
• Perform other duties as assigned by the manager

About Danaher

Danaher is a leading global life sciences, biotechnology, and diagnostics innovator, helping to solve many of the world's most important health challenges, ultimately improving quality of life for billions of people today, while setting the foundation for a healthier, more sustainable tomorrow. The Danaher ecosystem is made up of more than 15 businesses united by a shared commitment to innovate for tangible impact.

For more information, visit www.danaher.com.

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