- Medtronic (Los Angeles, CA)
- …7+ years of experience in Quality and/or Regulatory, including direct experience in MDR / vigilance systems implementation. OR Advanced degree with 5+ years of ... Understand current and upcoming Medical Device Reporting (MDRs) and EU Vigilance Reporting requirements by regulatory bodies and ensure adequate implementation or… more
- Caldera Medical (Westlake Village, CA)
- Sr. Regulatory Affairs Specialist 100% ONSITE in Westlake Village, California Sponsorship is not available for this role Caldera Medical's Mission - To Improve the ... Hiring Manager: In your role as a Sr. Regulatory specialist , you will develop and implement medical device regulatory...documentation for medical device approvals in compliance with EU MDR , MDSAP, NMPA, TGA, ANVISA, ANMAT, and other relevant… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …Life at Olympus (https://www.olympusamerica.com/careers) . **Job Description** As a Medical Safety Specialist II (MSSII) you will have an integral role in the ... knowledge and experience working with: + Various regulations (HIPPA, EU- MDR , FDA 21 CFR Part 803, 806, 820) +...+ Minimum of 2 years Medical Safety, risk management Vigilance or other Medical Device Experience (Medical Device preferred… more