Senior Associate Regulatory Affairs (Medical Devices)
Perrigo
Description OverviewWe are excited to be recruiting for an Senior Associate in Regulatory Affairs to be based in either Ghent, Rotterdam, London or Paris. Paris, France or Ghent working on our exciting Medical Device Portfolio.The main responsibilities of the role will be to work on a diverse range of Regulatory Affairs projects to meet business needs and ensure Regulatory Compliance of the company’s products with all relevant legislation around Medical Devices, including the MDD, the challenging new MDR, ISO 13485, ISO 14971 and other harmonized standards.Scope of the Role
Experience Required
Rotterdam, Zuid-Holland
Fri, 23 Aug 2024 22:32:58 GMT
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