Sr Regulatory Affairs Specialist Tracking Code 1864 Job Description Primary Function: Prepare submissions to obtain and maintain approvals for Active Implantable/Class III medical devices. Participate in activities to ensure compliance with worldwide regulatory requirements. Duties and Responsibilities: 1. Generate submissions (i.e. PMA, 510(k), PMA supplements, CE marking applications, product registrations, etc.) to obtain various worldwide approvals to commercially distribute products. Produc...
