Baxter Hiring Specialist Regulatory Affairs (Pharmacovigilance) – Ahmedabad
Global Pharma Career Opportunity
Baxter is hiring a Specialist – Regulatory Affairs (Pharmacovigilance) for its Ahmedabad location. This role offers an excellent opportunity to work on global safety reporting, regulatory submissions, and pharmacovigilance activities.
About Baxter
Baxter is a leading global healthcare company focused on improving patient outcomes through innovative medicines, medical devices, and healthcare solutions. With a presence worldwide, Baxter is known for quality, compliance, and patient safety.
Job Details
- Company: Baxter
- Position: Specialist, Regulatory Affairs
- Department: Regulatory Affairs & Pharmacovigilance
- Experience: 3–5 Years
- Qualification:
B.Pharm / M.Pharm / Pharm.D / M.Sc Life Sciences - Location: Ahmedabad, Gujarat
- Job Type: Full-Time
- Job ID: JR-204717
- Application Deadline: 30 June 2026
Role Overview
You will support global pharmacovigilance and regulatory affairs operations, focusing on safety reporting, risk management, and compliance activities.
Key Skills Required
- Regulatory Affairs & Pharmacovigilance
- PSUR, PBRER, PADER reporting
- Risk Management Plans (RMP)
- Signal Detection & Management
- CCDS / CCSI documentation
- XEVMPD database management
- Drug safety compliance
- Global regulatory submissions
Key Responsibilities
Aggregate Safety Reporting
- Prepare and review PSUR, PBRER, and PADER reports
- Support Aggregate Safety Governance activities
- Ensure timely submission of safety reports
Risk Management Plan (RMP)
- Develop and maintain RMP documents
- Coordinate with global teams
- Ensure compliance with submission timelines
Signal Management
- Identify and evaluate safety signals
- Update CCDS and CCSI documents
- Support label updates
Regulatory Activities
- Handle CO/NCO submissions
- Maintain XEVMPD database
- Monitor EV code approvals
- Support global regulatory compliance
Salary Expectations
₹8 LPA – ₹15 LPA (Approx.)
Depends on experience and internal company structure
Benefits & Perks
- Work with a global healthcare leader
- Exposure to international pharmacovigilance systems
- Career growth in regulatory affairs
- Advanced training & development programs
- Collaborative global work culture
- Opportunity to work on patient safety initiatives
How to Apply
Apply directly through the official Baxter careers page:
https://www.baxter.com/careers
Search for “Specialist Regulatory Affairs – Ahmedabad (JR-204717)”
Why Join Baxter?
- Global exposure in pharmacovigilance
- Work on critical drug safety programs
- Strong long-term career growth
- Opportunity to contribute to life-saving innovations
FAQs
Q1. Who can apply?
Candidates with 3–5 years of experience in Regulatory Affairs / Pharmacovigilance.
Q2. What qualifications are required?
B.Pharm, M.Pharm, Pharm.D, or Life Sciences degrees.
Q3. What is the job location?
Ahmedabad, Gujarat.
Q4. What skills are important?
Safety reporting, RMP, signal management, and regulatory compliance.
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