Medical Device - Regulatory Affairs Director
Descrizione dell'offerta
Medical Device – Regulatory Affairs Director
Responsibilities
- Line management of 10 Regulatory Line Managers
- Establish and implement regulatory strategies ensuring new and existing products comply with the latest global requirements
- Train the team on EMEA / FDA requirements
Qualifications
- Minimum 8 years in regulatory affairs in the medical device industry
- Minimum 4 years as Regulatory Affairs Manager / Director
- Experience with EMEA / FDA regulatory requirements
- Minimum 4–5 years of line management experience
- Availability to work 4 days in the office
Seniority level
- Director
Employment type
- Full‑time
Job function
- Legal
Industry
- Industrial Machinery Manufacturing