- Medtronic (Plymouth, MN)
- REGULATORY AFFAIRS SPECIALIST -...Affairs Specialist is responsible for worldwide regulatory activities to introduce new products (Class II ... and provide advice on regulatory requirements. The Regulatory Affairs Specialist is responsible...experience. Nice to have: + Experience working with Class II /III medical devices + Experience with regulatory … more
- J&J Family of Companies (St. Paul, MN)
- Senior Regulatory Affairs Specialist -...to obtain FDA clearance or approval of new Class II & III cardiovascular medical devices and improvements to ... Abiomed, part of Johnson & Johnson's MedTech, is recruiting for a Senior Regulatory Affairs Specialist . _Remote work options may be considered on a… more
- Medtronic (Minneapolis, MN)
- Position Description: Sr. Regulatory Affairs Specialist for Medtronic, Inc. Minneapolis, MN. Multiple positions available. Responsible for developing ... or 510(k) submissions for US Class III or Class II medical devices. Work on MDD (Medical Device Directive)...closely related field and 2 years' experience as a Regulatory Affairs Specialist , R&D Engineer… more
- Medtronic (Mounds View, MN)
- PRINCIPAL REGULATORY AFFAIRS SPECIALIST - CARDIAC SURGERY (Hybrid) Cardiac surgery represents end stage treatment in the care continuum for many ... technology and solutions Careers that Change Lives The Principal Regulatory Affairs Specialist is responsible...for worldwide governmental approval to introduce new products (Class II & III) to market, maintain existing products, provide… more
- Abbott (Plymouth, MN)
- …on with their lives. **The Opportunity** Abbott is seeking a passionate, experienced **Senior Regulatory Affairs Specialist ** to join our team on-site in ... Paul, MN. In this role, you will lead the preparation and submission for regulatory approvals and identify and resolve problems. You will provide regulatory … more