Offer summary
Qualifications:
Degree in Life Science, higher degree preferred, 7-10 years of Pharma work experience, Minimum 5 years in regulatory affairs for medical devices and drug/device combinations, Experience with global submissions and life-cycle management.
Key responsabilities:
- Contribute to dossier content and regulatory strategy development
- Prepare and manage regulatory documentation
- Lead continuous improvement and strategic thinking efforts
- Participate in office duties matching global team hours