Senior Regulatory Affairs Lead – Medical Devices
Listed on 2026-10-07
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Healthcare
Healthcare Compliance, Medical Science Liaison
Meridian Bioscience International Limited is seeking a Regulatory Affairs professional to support released products, including MDR investigations, post-market risk assessments, and CE Marking activities. You will liaise with QA, manufacturing, R&D, and customers to coordinate investigations and CAPA actions.
The role requires a Bachelor of Science in a related field and at least four years of regulatory experience in medical devices/pharma.
We have an opening for a Senior Regulatory Affairs Lead – Medical Devices in North Billerica, MA, United States within Bio & Pharmacology & Health, Management & Operations.
Full responsibilities and requirements are described in the listing above.
Learn more about the Senior Regulatory Affairs Lead – Medical Devices role in the description above.
We appreciate your interest in this position.
Join Meridian Bioscience International Limited and contribute to our ongoing work.
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