Torrent Pharmaceuticals Ltd., one of India’s leading pharmaceutical companies and a flagship entity of the Torrent Group, is inviting applications for the position of Executive – Regulatory Affairs (EU Market) at its R&D Centre in Gandhinagar, Gujarat. This opportunity is ideal for regulatory professionals with experience in EU dossier compilation, eCTD submissions, and post-approval variations who are seeking career growth in a globally recognized organization.
If you have hands-on exposure to EU regulatory procedures such as DCP, MRP, and National Phase handling, this role offers an excellent platform to strengthen your regulatory career.
🔍 Job Overview
- Company: Torrent Pharmaceuticals Ltd.
- Position: Executive – Regulatory Affairs (EU Market)
- Department: Regulatory Affairs
- Qualification: M.Pharm / M.Sc
- Experience: 2 to 7 Years
- Location: R&D Centre, Gandhinagar, Gujarat
- Last Date to Apply: 15 February 2026
🧾 Key Responsibilities
- Compilation of EU dossiers (Modules 1, 2, and 3)
- Handling DCP, MRP, and National procedures for EU submissions
- Management of National Phase submissions
- Preparation and submission of Post-Approval Variations to EU agencies
- Experience with eCTD compilation (added advantage)
- Regulatory support for solid oral dosage formulations
🎓 Eligibility Criteria
- M.Pharm or M.Sc in relevant discipline
- 2–7 years of experience in Formulation Regulatory Affairs
- Strong knowledge of EU regulatory guidelines
- Familiarity with electronic submissions (eCTD)
💼 Why Join Torrent Pharma?
- Work with a top-tier Indian pharmaceutical company
- Exposure to global regulatory markets (EU)
- Excellent learning and growth environment
- Competitive compensation and benefits
- Strong R&D and compliance culture
📩 How to Apply
Interested candidates can share their updated CV to:
Subject Line: Application for Executive – Regulatory Affairs (EU Market)