- Medtronic (Lafayette, CO)
- …in a more connected, compassionate world. **A Day in the Life** The Senior Regulatory Affairs Specialist (Sr. RAS) is responsible for working collaboratively ... EU Medical Device Regulation (MDR). The Sr. RAS translates regulatory requirements into actionable project or product...Minimum Requirements** + Bachelors degree with 4+ years of regulatory affairs experience in the medical device,… more
- Bausch + Lomb (Denver, CO)
- …preferred + Minimum of 8 years in recent experience in strategic pharmacuetical Regulatory Affairs . This position does not work with medical device, cosmetics ... labeling, adpromo areas. Serve as a strategic advisor to project teams, ensuring regulatory compliance, influencing key...and ability to see the business drivers outside of Regulatory Affairs + Ability to take innovative… more
- Sumitomo Pharma (Denver, CO)
- …ensure system validation is maintained. + Work closely with Clinical Operations and Regulatory Affairs to ensure compliance with regulatory requirements. + ... follow us on LinkedIn. The Trial Master File (TMF) Specialist will be responsible for ensuring that SMPA studies...quality concerns and oversee resolution of issues. + Develop project specific TMF plan and structure and update the… more