- Kelly Services (Bridgewater, NJ)
- ** EU - Medical Device Regulation (MDR) Specialist** Kelly(R) Science & Clinical is seeking an ** EU -MDR Specialist** for our client in Bridgewater, NJ. ... 2026 Pay is $57-61 an hour **Responsibilities:** + Contribute to the implementation of EU - Medical Device Regulation (MDR) and global regulation … more
- Integra LifeSciences (Princeton, NJ)
- …regulations, ISO 13485, the Canadian Medical Device Regulations (CMDR), the EU Medical Device Regulation , Japanese Pharmaceutical Affairs Law, ... + Demonstrated knowledge of FDA regulations, ISO 13485, CMDR, Medical Device Directive Regulation (93/42EEC),...standards. + Experience with direct contact with FDA and EU Notified Bodies. + Knowledge of process design and… more
- Integra LifeSciences (Princeton, NJ)
- …regulations, ISO 13485, the Canadian Medical Device Regulations (CMDR), the EU Medical Device Regulation , Japanese Pharmaceutical Affairs Law, ... + Demonstrated knowledge of FDA regulations, ISO 13485, CMDR, Medical Device Directive Regulation (93/42EEC),...standards. + Experience with direct contact with FDA and EU Notified Bodies. + Knowledge of process design and… more
- Terumo Medical Corporation (Somerset, NJ)
- …14971, ISO 11607, ISO 11135/ EN550, ISO 11137/ EN552 and the amended Medical Device Directive). + Assist with third party/regulatory audits (Customer, Notified ... 8, 2024 Req ID: 3503 Location: Somerset, NJ, US Company: Terumo Medical Corporation Department: Quality Systems & Compliance **Job Summary** The Quality Compliance… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …coverage, formulary and other patient access activities, clinical trials, continuing medical education activities, medical device reporting, quality ... 10 - 20 years' experience in healthcare law and regulation , preferably with medical devices. + Other...etc.): Position is remote, with expected travel to Japan, EU and China approximately 5 -15%. **Preferred:** + Must… more