Regulatory Affairs Post-approval Senior Associate-Europe - DEMO Global Services
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
At Demo SA, one of the world’s largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Senior Associate to join our team.
Requirements
- Bachelor or Master Degree in Pharmacy with 6-9 years of experience in Regulatory Affairs / CMC within a Pharmaceutical organization.
- Knowledge of CMC and global regulatory guidelines for Sterile (small & large volume parenteral, aqueous solution, lyophilized product, sterile powder etc) and oral solid/liquid dosage form.
- Strong organization skills, multi-tasking and able to meet deadlines.
- Effective communication and relationship management.
- Ability to work under pressure, resilience.
Benefits
- Competitive salary
- Continuous specialized training
- Career development
- Friendly working environment