As the European Authorised Representative (EAR), act as a liaison between Stryker Legal Manufacturers of medical devices located outside Europe and European Regulatory authorities, in matters related to product regulatory and quality compliance. […]
Serve as Management Representative for the EAR QMS under ISO 13485. Provide strategic direction, oversight and governance for processes related to Stryker's EAR role in close collaboration with Legal Manufacturers, Economic Operators and global stakeholders. […]
Ensure timely and effective MDR verification on behalf of the Economic Operators involved...