Global Medical Device Usability & Regulatory Lead
Listed on 2026-10-07
-
Healthcare
Healthcare Management, Healthcare Compliance
Sentec, a Swiss-American medical device company focusing on respiratory care, seeks a Usability and Regulatory Affairs Specialist to ensure products are safe, effective, and compliant globally. You will lead human factors activities and support regulatory submissions with engineering, clinical, and quality teams.
You will plan usability studies, maintain documentation, and drive risk mitigation. You will monitor FDA/EU requirements for continuous compliance and may travel up to five times per
We invite applications for the Global Medical Device Usability & Regulatory Lead position located in Lincoln, RI, United States.
This role is for the Global Medical Device Usability & Regulatory Lead role at Sentec.
We are seeking a motivated Global Medical Device Usability & Regulatory Lead to join Sentec in Lincoln, RI, United States.
Consider building your career as a Global Medical Device Usability & Regulatory Lead at Sentec.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).