Regulatory Affairs Post-Approval Manager (Europe) - DEMO Global Services Center
Demo S.A.Hyderabad, Telangana, India
Posted February 25, 2026
Full Time
About the Company
DEMO S.A. excels in developing and supplying pharmaceuticals, with Greece's largest production facility.
Job Description
We are looking for a Regulatory Affairs Post-Approval Manager to manage variations, life-cycle management, and compliance for authorised products for Europe and global markets.
Requirements
- Master or Bachelor degree in Pharmacy.
- 13+ years in Regulatory Affairs, with at least 9 years focused on EU post-approval activities, including variations and lifecycle management.
- Thorough understanding of European medicinal product regulation and procedures, EMA & CMDh guidance, and EU GMP guidelines.
Benefits
- Competitive salary and benefits
- Continuous specialized training
- Career development