- 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
- Philips (Plymouth, MN)
- **Principal Systems Engineer - Medical Device (Plymouth, MN)** In this role, you will contribute to a breakthrough cardiac ultrasound imaging solution that ... bridge between various functional teams, including R&D, manufacturing, and regulatory affairs, facilitating effective communication and alignment on systems… 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
- Actalent (Minneapolis, MN)
- …complex projects. Additional Skills & Qualifications + Additional certifications in clinical, regulatory , or quality fields. + Experience with venture capital, ... fundraising, and business development processes. + Experience designing or delivering clinical, regulatory , or quality training. + Experience setting up or… more
- Chemours (St. Paul, MN)
- …Engineering, Biological Science, Toxicology or comparable technical field + 5+ years of medical device regulatory compliance experience with respect to raw ... outside lawyers, consultants, industry associations, and local agencies on specific medical regulatory topics. + Coordinate and review customer… 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
- 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)
- … Affairs and Quality / Quality Operations within the FDA regulated Medical Device industry, including 3+ years of experience and a strong track ... Affairs will lead the Philips RespirTech InCourage Vest Therapy Regulatory Affairs and Quality teams in the... teams. + You have extensive experience/knowledge of global medical device regulations, requirements, and standards (ISO… more
- Medtronic (Mounds View, MN)
- …of promotional materials Must Have: Minimum Requirements Bachelors degree with 7+ years of medical device regulatory affairs experience OR An advanced degree ... RST stakeholders for R&D, QA, Operations, functional COEs, regional Regulatory and Quality , and the Medtronic Enterprise...with 5+ years of medical device regulatory affairs experience… more