In This Role, You Will Have The Opportunity To
- 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.
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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