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Macleods Pharmaceutical Ltd is inviting applications for the role of RMP Reviewer in its Pharmacovigilance – R&D Department based in Andheri, Mumbai.
This is an excellent opportunity for candidates with 1–2 years of experience in Pharmacovigilance, PSUR/PBRER/RMP review, and safety report quality checks.
If you’re looking to advance your PV career with one of India’s leading pharmaceutical companies, this role offers strong learning exposure and career growth.
Key Responsibilities
As an RMP Reviewer, the selected candidate will be responsible for:
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- Performing quality review of PSUR, PBRER, ACO, and RMP for Europe/UK, India, and ROW markets.
- Creating and maintaining PSUR/PBRER/ACO calendars and assigning timelines to team members.
- Tracking all periodic safety reports to ensure timely submission to RA/LRP or relevant authorities.
- Preparing and delivering SOPs and SGDs according to regulatory guidelines.
- Handling regulatory authority queries and preparing accurate, compliant responses.
- Using Microsoft Office tools (Word, PowerPoint) to prepare and organize documents.
Qualifications & Experience
- Education: M.Pharm (Pharmacology)
- Experience: 1–2 years in Pharmacovigilance / Safety Writing / RMP review
- Technical Skills: Microsoft Office (Word, PPT), regulatory documentation
- Note: Freshers are not eligible.
Why Join Macleods Pharma?
- Opportunity to work with a leading global pharmaceutical company
- Exposure to diverse safety regulatory markets (EU/UK, India, ROW)
- Skill development in advanced Pharmacovigilance processes
- Collaborative team environment in R&D – PV department
- Competitive compensation and growth pathways
How to Apply
Eligible candidates may email their updated resume to:
📩 adityab@macleodspharma.com
Subject Line: Applying for RMP Reviewer – (Your Name)
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