Executive Job at Torrent Pharma – Regulatory Affairs EU Market
An excellent Executive Job opportunity is now open with Torrent Pharma Careers for Regulatory Affairs professionals targeting the EU market. This Executive Job at Torrent Pharma Careers is based at the R&D Centre in Gandhinagar, Gujarat, and is ideal for candidates with experience in solid oral dosage formulation, regulatory affairs, and EU dossier handling.
- Job Position: R&D Centre – Gandhinagar (Gujarat)
- Location: Gandhinagar, Gujarat
About the Company
Torrent Pharma is a leading Indian pharmaceutical company with a strong global footprint across regulated and emerging markets. Executive Job opportunities at Torrent Pharma Careers provide professionals exposure to international regulatory environments, innovation-driven R&D, and high-quality compliance standards across global markets.
Job Description
This Executive Job at Torrent Pharma Careers is for the position of Executive – Regulatory Affairs (EU Market) at the R&D Centre in Gandhinagar, Gujarat. The role involves handling EU regulatory dossiers, national phase submissions, post-approval variations, and regulatory procedures such as DCP, MRP, and National. This Executive Job focuses on the formulation of regulatory activities for solid oral dosage forms for the EU market.
Key Responsibilities
- Job profile and exposure for the EU Market
- Formulation Regulatory experience of Solid oral Dosage form
- EU dossier compilation especially for Modules 1, 2 & 3
- Seasoned experience in handling various EU procedures like DCP, MRP,and National
- National phase handling for EU procedures
- Post approval variation compilation and filing to various EU agencies
- Experience of eCTD compilation would be an added advantage
Qualifications
- M.Pharm / M.Sc
- Relevant experience: 02 to 07 Years
Why Join This Company?
Choosing an Executive Job means becoming part of a globally respected pharmaceutical organization with strong expertise in regulated markets like the EU. Torrent Pharma offers a professional environment where regulatory professionals gain hands-on exposure to international dossiers, EU procedures (DCP, MRP, National), and post-approval variations.
