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Hiring Regulatory Affairs & Pharmacovigilance Roles
ProductLife Group
Remote India
3–7 Years
Regulatory + PV
Global Roles
🏢 About ProductLife Group
ProductLife Group (PLG) is a global consulting company specializing in Regulatory Affairs, Pharmacovigilance, and Quality Compliance. It supports pharmaceutical, biotech, and medical device companies worldwide with regulatory submissions, drug safety, and lifecycle management.
1️⃣ RA Officer (Associate Consultant) – JAPAC
- Work on TGA & Medsafe submissions
- Prepare CTD/eCTD dossiers
- Lifecycle management & GMP clearance
- Handle regulatory authority queries
Experience: 3+ Years (Regulatory Affairs)
Best For: Australia/New Zealand Regulatory roles
2️⃣ Regulatory Affairs Specialist – UK/EU
- Manage MAA (UK/EU), variations & renewals
- Handle MHRA & EMA submissions
- Work on eCTD lifecycle management
- Support audits & inspections
Experience: 3–7 Years
Tools: Veeva Vault, LorenZ, Trackwise
3️⃣ Case Specialist – Pharmacovigilance
- ICSR case processing & QC
- MedDRA & WHO Drug coding
- Causality assessment & narrative writing
- Signal detection & regulatory reporting
Experience: 4–5 Years (PV)
Best For: Drug Safety professionals
🎓 Eligibility
- B.Pharm / M.Pharm / PharmD / Life Sciences
- Strong knowledge of Regulatory or PV domain
- Good communication & documentation skills
💰 Salary (Estimated)
- ₹6 LPA – ₹14 LPA
- Depends on experience & role
🚀 Career Growth
- Global Regulatory Affairs roles
- Pharmacovigilance Specialist
- Regulatory Strategy & Consulting
- Drug Safety Scientist
🎯 Interview Tips
- Revise CTD/eCTD structure
- Understand ICSR workflow & MedDRA
- Learn global agencies (EMA, MHRA, TGA)
- Prepare lifecycle management scenarios
📚 Useful Resources:
📌 Note Before You Apply:
Kindly read the role requirements carefully and select the position matching your experience.
Kindly read the role requirements carefully and select the position matching your experience.
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