The Director, Regulatory Affairs, EU is responsible for leading and executing regional and global regulatory strategies to support drug and device development
Job Summary
The Director, Regulatory Affairs, EU is responsible for leading and executing regional and global regulatory strategies to support drug and device development.
This role ensures compliance with European and international regulations while enabling efficient clinical development and successful project delivery.
We provide opportunities for personal and professional growth in a rewarding environment.
Matching Summary
The Director, Regulatory Affairs, EU is responsible for leading and executing regional and global regulatory strategies to support drug and device development.
Skills & Requirements
Must-have
European and global regulatory strategy
EMA and national authorities
drug and device development
clinical development journey
regulatory documents development
Nice-to-have
collaboration and quality
making a difference in patients' lives
problem-solving skills
Key Requirements
Advanced degree in Life Sciences, Pharmacy, Medicine
Significant experience in regulatory affairs
Strong knowledge of European regulatory requirements