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Hiring Regulatory Affairs / Pharmacovigilance Specialist
🏢 Baxter
📍 Ahmedabad
⏳ 2–6 Years
💊 Regulatory Affairs / PV
Baxter is hiring a Regulatory Affairs / Pharmacovigilance Specialist. This role offers exposure to PSUR, PBRER, RMP, Signal Management, and Global Regulatory Submissions.
👉 Career Path: B.Pharm Career Options
📋 Job Overview
- Role: Regulatory Affairs Specialist
- Company: Baxter
- Location: Ahmedabad
- Experience: 2–6 Years
- Qualification: B.Pharm / M.Pharm / PharmD
- Last Date: 23 April 2026
📌 Key Responsibilities
- Prepare PSUR, PBRER, PADER reports
- Handle regulatory submissions
- Work on RMP & signal management
- Maintain XEVMPD database
- Support global compliance activities
💻 Required Skills
- Regulatory Affairs & PV knowledge
- PSUR / PBRER expertise
- EudraVigilance exposure
- Strong documentation skills
💡 Interview Tips
- Understand PSUR & PBRER
- Revise RMP & signal detection
- PV Interview Questions
- PV Quiz Practice
📚 Must Read Resources
💰 Salary & Growth
- ₹6 – ₹12 LPA
- Growth → RA Specialist → Manager
- Salary Guide
📌 Apply before 23 April 2026
📌 Strong PV + RA knowledge required
🚀 Job Application Link
📌 Important Note Before You Apply:
Kindly read the full job description carefully before applying. Ensure your profile aligns with Regulatory Affairs (RA) operations, lifecycle maintenance, preparation and submission of regulatory dossiers, global health authority compliance tracking, and post-approval variations management before proceeding.
Kindly read the full job description carefully before applying. Ensure your profile aligns with Regulatory Affairs (RA) operations, lifecycle maintenance, preparation and submission of regulatory dossiers, global health authority compliance tracking, and post-approval variations management before proceeding.
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