Medical Device Regulatory Affairs Specialist
Listed on 2026-10-21
-
Healthcare
Healthcare Compliance, Medical Science Liaison, Medical Device Industry
Actalent is seeking a Regulatory Affairs Specialist to support regulatory compliance, product registrations, and submissions for medical devices in the U.S. and internationally. Based in Kendall, FL, this role offers exposure to QA, R&D, and regulatory teams in a growing medical device organization.
The ideal candidate has strong regulatory knowledge, excellent writing skills, and comfort coordinating with agencies across markets; bilingual English/Spanish is a plus.
We have an opening for a Medical Device Regulatory Affairs Specialist in Miami, FL, United States within Legal, Management & Operations.
Learn more about the Medical Device Regulatory Affairs Specialist role in the description above.
We appreciate your interest in this position.
Join Actalent and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
(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).