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.
#J-18808-LjbffrSenior Regulatory Affairs Lead in north billerica at Unknown Company
This position is listed as full time and onsite.