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Torrent Pharmaceuticals is seeking a skilled Executive – Biopharmaceutics (Clinical Research) to join its dynamic R&D team in Gandhinagar. The role focuses on clinical research operations, regulatory compliance, and study documentation for biopharmaceutical products.
Key Responsibilities:
- Conduct feasibility assessments and evaluate new products.
- Perform literature reviews and design BA/BE (Bioavailability/Bioequivalence) studies.
- Monitor BE studies and ensure protocol adherence.
- Prepare and review regulatory submission documents (BENOC, Import License Applications).
- Maintain study documentation for clinical and non-clinical overviews.
- Review BE study protocols, reports, and Informed Consent Forms (ICF).
- Draft medical/scientific write-ups for dossiers.
- Coordinate adverse event reporting and safety updates for regulatory agencies.
2. About Torrent Pharmaceuticals
Torrent Pharma is a leading Indian multinational pharmaceutical company with a strong presence in R&D, manufacturing, and marketing of high-quality formulations. Known for its innovation in cardiovascular, CNS, and diabetic therapeutics, Torrent’s Gandhinagar R&D centre is a hub for cutting-edge clinical research.
3. Eligibility Criteria
- Education: M.Pharm in Pharmacology (mandatory).
- Experience: 2–5 years in clinical research, BA/BE studies, or regulatory submissions.
- Skills:
- Proficiency in regulatory guidelines (CDSCO, ICH-GCP).
- Strong documentation and analytical skills.
- Experience in study monitoring and dossier preparation.
4. How to Apply
Interested candidates meeting the criteria can email their updated CV to:
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- Megha Maheshwari: meghamaheshwari@torrentpharma.com
- Vilsha Shah: vilshashah@torrentpharma.com
Subject Line: “Application for Executive – Biopharmaceutics (Ref: Pharmabharat.com)”
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