Company: AbbVie
Location: Maidenhead, United Kingdom
Type: Full-time | Regulatory Affairs
About the Role
AbbVie seeks a Senior Manager of Regulatory Affairs to lead regulatory strategy for medical devices and combination products across the EU and UK markets.
Requirements
- 8+ years in regulatory affairs for medical devices
- EU MDR, IVDR, and UK MDR 2002 expertise
- Clinical research and regulatory submission experience
Apply: View on EuroPharmaJobs