About this role
Principal Regulatory Affairs Specialist - EMEA (Cluster Partner) at CooperVision. Location: Southampton or Gorinchem or Gothenburg. Role: reviewing documents, maintaining files, coaching staff Requirements: 6+ years medical device regulatory experience with MDD/MDR knowledge, technical writing, regulatory submissions, ISO 13485 understanding, and strong communication and IT skills. Category: Legal and Compliance Seniority: Senior Level Tools: Microsoft Word, Microsoft Excel, Microsoft Outlook, Agile Project Management system Commitment: Full Time Workplace: Onsite Languages: English