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Develop and implement Quality Systems processes to support medical device development, including system-level integration.
Build and grow a high-performance team through recruiting, coaching, engagement, and performance management.
Provide and analyze quality metrics for customer complaints and participate in internal and external audits as a subject matter expert for Systems Quality.
Ensure design control requirements are met, including design verification, validation, specification/procedure development, risk management, and design review.
Lead risk analysis teams and develop risk analysis standards at appropriate points in the product development lifecycle.
Coordinate communications with internal customers to ensure requirements are understood and component/product performance is appropriately managed.
Job ID: 144165197