- Medtronic (Mounds View, MN)
- …Surgical product portfolio achieves initial European Union Medical Device Regulation ( EU MDR ) and UK Conformity Assessed (UKCA). This Program Manager ... of interdependent information to create recommendations for action and program success. + Cultivate a broad understanding of Medtronic's...+ PMP or PgMP certification + Strong knowledge of EU MDR and UKCA regulations + Experience… more
- Philips (Plymouth, MN)
- **R&D Program Manager - Medical Device NPD (Plymouth, MN)** We are seeking a highly motivated and experienced Program Manager with a background in ... professional experience with a minimum of 7 years in program /project management within the medical device, healthcare, or similarly...and regulatory and quality standards (eg, FDA, ISO 13485, EU MDR ). Proficiency with project management tools… more
- Medtronic (Fridley, MN)
- …design and risk management. + Contribute human factors documentation to support FDA and EU MDR regulatory submissions. **Location** : Fridley, MN + _This is an ... human factors engineering activities for the Wearable External Neurostimulator (WENS) program , supporting our Spinal Cord Stimulation (SCS) therapies. In this role,… more
- Medtronic (Minneapolis, MN)
- …+ Knowledge and understanding of Good Clinical Practices, Post Market Surveillance, EU MDR Regulation, Quality Management Systems, Risk Management and other ... interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements… more