Quality Engineer II: Medical Device Quality & Process

A leading medical device company in Sunnyvale seeks a Quality Engineer II to support product development, ensuring compliance with quality standards and regulatory requirements. This role involves collaborating with cross-functional teams, monitoring project progress, and implementing quality processes such as GMP and FDA requirements. The ideal candidate will have a strong understanding of quality engineering principles, experience with statistical analysis, and familiarity with FDA documentation.

Contribute to a dynamic team focused on delivering high-quality medical devices.
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