Senior Regulatory Affairs Lead - Medical Devices (US/EU)

Medtronic is seeking a Senior Regulatory Affairs Specialist in North Haven, Connecticut, to oversee regulatory activities for their product portfolio. The ideal candidate will have a Bachelor's degree and 4+ years of relevant experience in regulatory affairs in the medical device, biotech, or pharmaceutical industries. Responsibilities include preparing regulatory submissions, providing cross-functional regulatory guidance, and maintaining compliance with US and EU regulations. The role offers a competitive salary and comprehensive benefits including health insurance and a 401(k) plan.
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