Medtronic plc is seeking a Senior Regulatory Affairs Specialist to lead worldwide product registrations. The role focuses on preparing submissions to the FDA, EU MDR, and other global agencies, and collaborating with cross-functional teams to resolve regulatory issues and maintain licenses. You will interact with regulators, support post-market activities, and contribute to the global regulatory strategy for high-risk medical devices, leveraging your experience to ensure timely market approvals. #J-18808-Ljbffr