- Medtronic (Mounds View, MN)
- …Bachelor's degree in a technical discipline + Minimum 2 years of medical device , engineering, quality or regulatory experience with Bachelor's degree + ... Or 0 years of medical device regulatory experience with...13485, and other global regulatory requirements and quality standards Supporting device submissions + Strong… 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 managing ... experience with a minimum of 7 years in program/project management within the medical device , healthcare, or similarly regulated industry, with proven experience… more
- Abbott (Maple Grove, MN)
- …managing projects related to harmonized regulatory activities in the Abbott's medical device division. As an individual contributor, the function of a ... medical products, nutritionals). 2-3 years of experience in regulatory preferred but may consider quality assurance,...- Regulatory Review + EU and US medical device compliance + Project management skills… more
- Abbott (Maple Grove, MN)
- …managing projects related to harmonized regulatory activities in the Abbott's medical device division. As an individual contributor, the function of a ... (eg, medical products, nutritionals). 2-5 years of experience in regulatory preferred but may consider quality assurance, research and development/support,… more
- Abbott (Plymouth, MN)
- …of international regulatory affiliates. + Compile, prepare, review and submit medical device submissions to regulatory agencies + Interfaces directly ... scientific affairs function. **Preferred** **Qualifications** + 4+ years of related regulatory submission experience from medical device , pharmaceutical,… more
- Medtronic (Mounds View, MN)
- …profile._ + Bachelor's degree required with a minimum of 2 years of experience in regulatory affairs in the medical device industry Or + Advanced degree ... Device Directive (MDD), Medical Device Regulation (MDR), and/or other global regulatory requirements and quality standards. + Effective negotiation… more
- Abbott (St. Paul, MN)
- …submissions. + Must be familiar with relevant regulatory requirements for medical devices including Quality Systems standards and clinical investigations. + ... necessary detail. + Maintains ongoing surveillance and analysis of all pertinent medical device regulations to ensure submission requirements worldwide are… more
- Abbott (St. Paul, MN)
- …for diversity, working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more ... disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives… more
- Philips (Plymouth, MN)
- …of 8+ years' Regulatory Affairs experience within FDA regulated Medical Device /HealthTech product environments. Experience with Software as Medical ... reviewed with the RA management. + Driving improvement in regulatory aspects of the Quality Management System...Technical Documentation, 510(k), De Novo, PMA, and registrations of medical devices globally. + You're able to work in… more
- Abbott (Plymouth, MN)
- …years' experience in a regulated industry (eg, medical products, nutritionals). Regulatory area is preferred but may consider quality assurance, research and ... to various international affiliates. + Maintains pertinent domestic and international medical device regulations to ensure submission requirements world-wide are… more