- Medtronic (Minneapolis, MN)
- … support for Class I, II and Class III medical devices. The Sr Principal Regulatory Affairs Specialist is responsible for activities to launching new ... the diagnosis and treatment of atrial fibrillation. The Sr Principal Regulatory Affairs Specialist will...of relevant experience + Or minimum 5 years of medical device regulatory affairs experience with Master's… more
- Philips (Plymouth, MN)
- The Principal Regulatory Affairs Specialist will play a critical role in preparing comprehensive regulatory strategies for complex new devices and post ... + You've acquired a minimum of 7 years' experience in FDA regulated Medical Device Regulatory Affairs , with proven expertise in US FDA 510K, China NMPA, and EU… more
- Teleflex (Maple Grove, MN)
- Regulatory Affairs Specialist **Date:** Sep 14, 2024 **Location:** Maple Grove, MN, US **Company:** Teleflex **Expected Travel** : Up to 10% **Requisition ID** ... that make a difference in patients' lives. **Position Summary** The Regulatory Affairs Specialist will develop strategies, submissions, and regulatory reviews of… more
- Edwards Lifesciences (St. Paul, MN)
- …to pioneering technologies for patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and ... and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to… more