Regulatory Affairs Specialist, Medical Devices; Onsite
Listed on 2026-10-16
-
Healthcare
Healthcare Compliance, Medical Device Industry, Medical Science Liaison
Medtronic is seeking a Regulatory Affairs Specialist to support regulatory strategy, submissions, and compliance for global medical devices. You will partner with engineering, quality, clinical, and manufacturing teams to ensure registrations and maintain compliance across markets.
The role focuses on preparing submissions (510(k), PMA, EU MDR) and guiding product changes through regulatory processes while collaborating with international teams. Onsite in Minnesota with regular office presence.
We would love to welcome a new Regulatory Affairs Specialist, Medical Devices (Onsite) to our team in Minneapolis, MN, United States.
The Regulatory Affairs Specialist, Medical Devices (Onsite) position in the Legal, Management & Operations field is open for applications.
We have an opening for a Regulatory Affairs Specialist, Medical Devices (Onsite) in Minneapolis, MN, United States within Legal, Management & Operations.
This role, Regulatory Affairs Specialist, Medical Devices (Onsite) at Medtronic, could be your next move.
(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).