Senior Regulatory Affairs Specialist - Onsite
Medtronic · Irvine, CA
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Role summary
This senior regulatory affairs specialist role supports compliance and lifecycle management for a portfolio of neurovascular medical devices at Medtronic's Irvine facility. The position involves preparing FDA submissions, managing EU MDR documentation, assessing product changes for regulatory impact, and collaborating across engineering, quality, and clinical teams. Requires a bachelor's degree in science or engineering with 4+ years of medical device regulatory experience, or an advanced degree with 2+ years in the field.
Privacy & handoff
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