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The Associate MDR/Vigilance Specialist at Medtronic is responsible for documenting and evaluating product feedback and analysis results for Medtronic products. This role involves determining complaint status and regulatory reporting status in accordance with US and OUS regulatory guidelines. The specialist compiles regulatory agency reports for submission and monitors complaint activity to ensure timely review and closure of complaints, contributing to the development of life-restoring therapies and healthcare solutions in the Neuroscience Portfolio group.