Torrent Hiring Regulatory Affairs Executive
- Company Overview
- Job Role & Responsibilities
- Executive – Regulatory Affairs (EU Market)
- Key Responsibilities
- Eligibility / Qualifications
- Educational Qualification
- Relevant Experience
- Relevant Courses
- Location & Salary
- Application Process
- Why Join Torrent Pharma Regulatory Affairs?
- Frequently Asked Questions (FAQs)
M.Pharm/M.Sc Regulatory Affairs Executive – EU | Gandhinagar
Hiring M.Pharm/M.Sc candidates for Regulatory Affairs Executive (EU Market) role in Gandhinagar. 2–7 years experience required.
Torrent Pharmaceuticals is inviting experienced regulatory professionals to join its high-impact Regulatory Affairs team at the R&D Centre in Gandhinagar, Gujarat. This opportunity is ideal for candidates with strong exposure to EU regulatory submissions who want to work with a globally respected pharmaceutical organization known for scientific rigor, compliance excellence, and international market leadership.
Company Overview
Torrent Pharmaceuticals Ltd. is one of India’s leading multinational pharmaceutical companies with a strong presence across regulated and emerging markets. Known for its robust R&D capabilities, Torrent has consistently delivered high-quality formulations across cardiovascular, CNS, gastro-intestinal, diabetology, oncology, and women’s healthcare segments. The company’s R&D Centre at Gandhinagar plays a critical role in global regulatory strategy, dossier development, and lifecycle management for Europe and other regulated markets.
By joining Torrent Pharma’s Regulatory Affairs function, professionals become part of a compliance-driven environment that directly supports patient access to safe, effective, and affordable medicines across international markets.
Job Role & Responsibilities
Executive – Regulatory Affairs (EU Market)
The selected candidate will be responsible for end-to-end regulatory activities related to European markets, with a strong focus on solid oral dosage formulations.
Key Responsibilities
- Preparation, review, and submission of EU regulatory dossiers for solid oral dosage forms
- Compilation of CTD and eCTD dossiers with strong hands-on exposure to Modules 1, 2, and 3
- Handling EU regulatory procedures including DCP, MRP, and National submissions
- Management of national phase submissions for EU procedures
- Preparation and submission of post-approval variations, renewals, and lifecycle management dossiers
- Coordination with internal stakeholders such as R&D, QA, and manufacturing teams
- Response to regulatory queries and deficiency letters from EU agencies
- Ensuring compliance with current EU regulatory guidelines and timelines
This role directly contributes to Torrent Pharma’s ability to launch and maintain products in highly regulated European markets.
Eligibility / Qualifications
Educational Qualification
- M.Pharm, M.Sc
Relevant Experience
- 2 to 7 years of hands-on experience in Regulatory Affairs
- Mandatory exposure to EU market regulatory submissions
- Strong experience in formulation regulatory affairs for solid oral dosage forms
- Practical knowledge of EU procedures: DCP, MRP, and National
- Experience in eCTD compilation is an added advantage
Relevant Courses
M.Pharm (Pharmaceutics, Pharmaceutical Regulatory Affairs, Quality Assurance), M.Sc (Pharmaceutical Sciences, Chemistry, Life Sciences)
Location & Salary
- Job Location: R&D Centre, Gandhinagar, Gujarat
- Salary: Competitive and commensurate with experience (as per industry standards)
Application Process
Interested and eligible candidates can apply by sharing their updated resume via email:
Candidates are advised to mention “Executive – Regulatory Affairs (EU Market)” in the subject line for faster shortlisting.
Why Join Torrent Pharma Regulatory Affairs?
- Work on regulated EU markets with real ownership of dossiers
- Exposure to global regulatory strategy and lifecycle management
- Strong compliance culture aligned with EMA and EU authority expectations
- Career growth within a scientifically driven, globally respected organization
Frequently Asked Questions (FAQs)
Q1. Is EU market experience mandatory for this role?
Yes. Candidates must have hands-on experience with EU regulatory procedures such as DCP, MRP, or National submissions.
Q2. Are freshers eligible for this position?
No. This role is strictly for experienced professionals with 2–7 years of regulatory affairs experience.
Q3. Is eCTD experience mandatory?
eCTD experience is preferred but not mandatory. Strong CTD dossier experience is essential.
Q4. What dosage forms does this role focus on?
The role primarily focuses on solid oral dosage forms.
Q5. Where is the job location?
The position is based at Torrent Pharma’s R&D Centre in Gandhinagar, Gujarat.
| Company | Torrent Pharmaceuticals Ltd. |
|---|---|
| Vacancies | Executive – Regulatory Affairs (EU Market) |
| Required Education | M.Pharm, M.Sc |
| Experience | 2–7 Years (EU Regulatory Affairs) |
To apply for this job email your details to nitinsingh@torrentpharma.com
