Senior Global Regulatory Affairs Specialist – Med Devices
Listed on 2026-10-07
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Healthcare
Healthcare Compliance
Atri Cure, Inc. is seeking a Senior Regulatory Affairs Specialist to prepare and submit regulatory documentation worldwide, including US 510(k) and PMA supplements, and to support EU, Canada, Australia, Brazil, Japan, and other markets.
You will serve as regulatory lead on new product development and post-market changes, collaborate with FDA and other authorities, and ensure quality documentation across sterilization, biocompatibility, electrical safety.
This posting is for the Senior Global Regulatory Affairs Specialist – Med Devices role at Atri Cure, Inc., based in Mason, OH, United States.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Mason, OH, United States.
This opportunity is part of our work in Bio & Pharmacology & Health, Management & Operations.
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