Piramal Pharma Limited is a leading global pharmaceutical company committed to delivering high-quality, innovative healthcare solutions. With a strong presence in over 100 countries, Piramal Pharma focuses on critical care, consumer healthcare, and complex generics. The company is known for its robust pharmacovigilance system, ensuring drug safety and regulatory compliance.
📍 Location: Mumbai, India
📅 Experience Required: 2-4 years Freshers may apply
🎓 Qualification: B.Pharm / M.Pharm
Detailed Job Description
Key Responsibilities:
✔ End-to-End Case Management:
- Handling ICSR (Individual Case Safety Report) processing, including case receipt, follow-up, database entry, and submission to regulatory authorities.
- Literature screening for safety data.
- Authoring aggregate reports like PADERs, PBRERs, and PSURs.
✔ Regulatory Compliance & Reporting:
- Reconciliation of ICSRs and mailbox management.
- Preparing compliance reports for QPPV (Qualified Person for Pharmacovigilance).
- Assisting in audits and inspections.
✔ Stakeholder Coordination:
- Collaborating with internal teams (Quality, Regulatory Affairs, Supply Chain) and external vendors.
- Responding to regulatory queries on drug safety.
Eligibility Criteria
✅ Education: B.Pharm / M.Pharm (Freshers may apply but 2-4 years preferred).
✅ Experience:
- Minimum 1 year in ICSR processing & literature screening.
- Experience in PADERs, PBRERs drafting is a plus.
✅ Skills Required: - Strong knowledge of pharmacovigilance regulations (GVP, ICH-GCP).
- Proficiency in Microsoft Office (Word, Excel, PowerPoint).
- Excellent communication & multitasking abilities.
Benefits & Work Culture
✨ Competitive salary (Disclosed during hiring process).
✨ Career growth in a globally recognized pharma company.
✨ Work-life balance with structured shifts.
✨ Learning opportunities in drug safety & regulatory compliance.
How to Apply?
