My client is a growing medical device company looking for a Regulatory Affairs Manager to join their QA/RA team based in southern part of Sweden.
Responsibilities: Development of the regulatory / filing strategy for the licensing of medical Devices in the EU and globally Development of the technical strategy & technical content for the licensing of medical Devices Collate and analyse regulatory intelligence and developing technical and regulatory positions Lead Regulatory Agency and/or Notified Body interactions in EU and/or other continents Lead and manage a team
BA/BS in Scientific discipline or equivalent work experience RAC certification desired
Working knowledge of Medical Device Regulations (international a plus) interpersonal, written, oral, communication, organizational and planning skills, Previous managerial experience
For more information please contact Noemie Oliva on +44 1293 776644 or email me at:-email@example.com