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READ MORERegulatory Affairs
The Regulatory Affairs Division at M3 specialises in providing expert recruitment services within the Regulatory Affairs, QA and Drug Safety/Pharmacovigilance specialities. This specialist team of five consultants supports clients within the Pharmaceutical, Biotech, Clinical Research and Medical Device industries, recruiting candidates on a Contract, Permanent and Retained basis throughout Europe and beyond.
We recruit for a wide range of positions including:
- Regulatory ExecutiveAssociate/Officer/Specialist
- Regulatory Consultant/Contractor
- Senior Regulatory Affairs Executive/Officer/Associate
- Regulatory Affairs Manager
- Senior Regulatory Affairs Manager
- Associate Director Regulatory Affairs
- Director Regulatory Affairs
- Senior Director Regulatory Affairs
- Vice President Regulatory Affairs
- Drug Safety/Pharmacovigilance Associate/Officer/Executive/Scientist
- Drug Safety/Pharmacovigilance Contractor/Consultant
- Drug Safety/Pharmacovigilance Manager
- Associate Director/AD Drug Safety/Pharmacovigilance
- Director/Head of Drug Safety/Pharmacovigilance
- Vice President Drug Safety/Pharmacovigilance
- QA Associate/Officer/Executive
- QA Auditor
- QA Manager
- QA Contractor/Consultant
- QA Director
We have a very wide geographic scope and have recruited in the following Countries: UK, Irelan, Spain, Portugal, France, Belgium, The Netherlands, Poland, Germany, Italy, Switzerland, Austria, Greece, Malta, Finland, Bulgaria, Hungary, Lithuania, Latvia, Estonia, Belarus, Ukraine, Serbia and Montenegro, Croatia, Slovenia, Bosnia and Herzegovina, Macedonia, Romania, Czech Republic, Slovakia, Denmark, Sweden and Norway.
If you have needs for any of the staff above or any other roles within Regulatory Affairs then please contact our Head of Regulatory Recruitment, Neal Panting on +44 1483 228190 or neal.panting@m3pharma.com