Regulatory Affairs Strategist – Medical Devices; Hybrid

Clin Choice is seeking an Associate, Regulatory Affairs for a hybrid role in Cincinnati, OH. The candidate will manage regulatory documents, submissions, and communications across global registrations, ensuring accuracy and timely delivery.

Requirements include a Life Sciences degree and 1 year in medical device regulatory affairs (or 3 years RA/related experience), knowledge of FDA QSR, ISO 13485, EU MDR, and strong documentation skills. Proficiency in Microsoft Office is essential.

This opportunity is for the Regulatory Affairs Strategist – Medical Devices (Hybrid) role at Clin Choice.

Consider building your career as a Regulatory Affairs Strategist – Medical Devices (Hybrid) at Clin Choice.

The Regulatory Affairs Strategist – Medical Devices (Hybrid) position in the Legal, Management & Operations field is open for applications.

We have an opening for a Regulatory Affairs Strategist – Medical Devices (Hybrid) in Cincinnati, OH, United States within Legal, Management & Operations.