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Job description
Meridian Bioscience Inc. is seeking a Regulatory Affairs professional to support released products, manage MDR investigations, post market risk assessments, and maintain technical files for CE marking.
The role liaises with QA, manufacturing, R&D, and customers to coordinate complaint investigations and CAPAs. Responsibilities include updating technical files for FDA and EU submissions, evaluating regulatory impact of design changes, and guiding labeling activities to ensure compliance.
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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.