Global Regulatory Affairs Specialist, Medical Devices
Listed on 2026-10-21
-
Healthcare
Healthcare Compliance, Medical Science Liaison
Medtronic is seeking a Regulatory Affairs Specialist based at the Rice Creek East campus in Minnesota, with an onsite model requiring four days per week in the office. You will support regulatory strategy, submissions, approvals, and lifecycle management for global medical devices, partnering with cross-functional teams and international regulators.
The role focuses on preparing US/EU/Canada submissions, maintaining registrations, and ensuring ongoing compliance across product life cycles in
The Global Regulatory Affairs Specialist, Medical Devices position in the Legal, Management & Operations field is open for applications.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the Global Regulatory Affairs Specialist, Medical Devices role at Medtronic plc, based in Fridley, MN, United States.
We are looking to fill the Global Regulatory Affairs Specialist, Medical Devices position at Medtronic plc in Fridley, MN, United States.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).