Main Accountabilities Coordinate product certification activities for all APTIV CS product lines. Act as the main interface for certification and regulatory compliance topics towards customers, authorities, and certification bodies. Coordinate certification requirements with Engineering, Quality, Manufacturing,
Overview In this role you will support CE marking for IVD devices by managing schemes, delivering expert technical reviews, and guiding QMS and regulatory activities. You’ll mentor healthcare personnel and collaborate with the commercial team to enable compliant,
Overview As Technical Specialist & Scheme Manager, you will support the certification of active medical devices for the European market. You will review technical and clinical documentation, manage certification activities, and provide regulatory guidance across CE marking schemes.