Global Regulatory Affairs Specialist - Medical Devices
Medtronic
Medtronic in Minnesota seeks a Regulatory Affairs Specialist in the Access and Instruments unit to support regulatory strategy, prepare submissions, and ensure compliance across global markets. You will partner with product teams, manage change effects, support audits, and stay current with EU MDR and ISO standards while advancing patient‑centric medical technologies. Join a collaborative team that navigates complex regulatory requirements and drives regulatory excellence throughout the product #J-18808-Ljbffr
Vacancy posted 2 days ago
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