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Job description
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.
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Worksite address
north billerica, MA, 01862, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.