Job Description
Roles & Responsibilities:
- Assist the Global PV RP (Pharmacovigilance Responsible Person) in coordinating worldwide PV activities.
- Support in maintaining Pharmacovigilance System Master File (PSMF) and Detailed Description of Pharmacovigilance System (DDPS).
- Process Adverse Drug Reaction (ADR) reports and ensure timely regulatory submissions.
- Prepare and review aggregate reports (PSUR, PBRER, DSUR, PADER, REMS) for compliance.
- Respond to medical inquiries from healthcare professionals (HCPs) and non-HCPs.
- Assist in maintaining and updating the validated safety database per regulatory standards.
Preferred Candidate Profile
- Education: M.Pharm (Pharmacy)
- Experience: 1-5 years in Pharmacovigilance (Drug Safety, ADR Reporting, Aggregate Reports)
- Skills Required:
- Knowledge of global pharmacovigilance regulations (GVP, ICH, FDA, EMA).
- Experience in safety database management (Argus, VigiFlow, etc.).
- Strong documentation & compliance skills.
- Good communication & analytical abilities.
About Torrent Pharmaceuticals
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Torrent Pharmaceuticals is a leading Indian multinational pharmaceutical company known for its strong presence in cardiovascular, CNS, gastrointestinal, and diabetic therapeutic segments. With a global footprint, Torrent is recognized for its innovation, compliance, and patient-centric approach.
🔹 Why Join Torrent Pharma?
- Work in a reputed & growing pharmaceutical firm.
- Global exposure in pharmacovigilance operations.
- Learning & career growth opportunities.
How to Apply?
Interested candidates can share their updated CV at:
📧 Email: vilshashah@torrentpharma.com
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