Dr. Reddy’s Laboratories: Hiring Experienced Pharmacovigilance (PV) & Drug Safety Professionals

Dr. Reddy’s Laboratories Ltd.—a leading multinational pharmaceutical enterprise with global footprints across US, Europe, and Emerging Markets—is actively hiring experienced Pharmacovigilance (PV) & Drug Safety professionals for its Global Safety & Regulatory Operations unit.

Key Job Details

• Company Name: Dr. Reddy’s Laboratories Ltd.
• Designation: Safety Analyst / Drug Safety Associate / Senior Specialist – Pharmacovigilance
• Target Experience: 2 to 6 Years in Individual Case Safety Report (ICSR) Processing / Aggregate Safety Reporting
• Educational Qualification: B.Pharm / M.Pharm / Pharm.D / MBBS / BDS / M.Sc (Life Sciences)
• Job Location: Hyderabad (Telangana) / Remote (Hybrid)
• Employment Type: Full-Time, Permanent

Detailed Department Breakdown & Scope of Work

1. ICSR Case Processing & Medical Assessment

• End-to-end processing of Individual Case Safety Reports (ICSRs) from clinical trials (spontaneous, solicited) and post-marketing sources using industry-standard safety databases (Argus Safety / ARISg).
• Performing MedDRA coding of adverse event terms, medical history, and suspect drugs; drafting comprehensive narrative writing for serious and non-serious cases.
• Evaluation of causality, unexpectedness, and expectedness against Reference Safety Information (RSI), USPI, SmPC, and Investigator's Brochure (IB).

2. Aggregate Safety Reporting & Signal Management

• Assisting in authoring and medical review of aggregate safety documents including DSUR (Development Safety Update Reports), PSUR/PBRER (Periodic Safety Update Reports), and PADER.
• Performing signal detection, risk management plan (RMP) reviews, and adverse event surveillance across global health authority platforms (USFDA, EMA, MHRA, CDSCO).
• Handling safety query responses and supporting regulatory inspections and internal PV audits.

Selection & Interview Process

1. Profile Shortlisting: Technical screening based on hands-on Argus Safety usage, MedDRA coding proficiency, and ICSR workflow understanding.
2. Technical Interview: In-depth evaluation covering ICH-E2D guidelines, GVP modules, narrative framing, causality assessment models, and SAE handling timelines.
3. HR & Line Management Review: Notice period review, hybrid work arrangement discussions, and compensation alignment.

📋 Checklist of Documents Required

• Updated Resume / CV (2 Copies)
• Academic Marksheets & Degree Certificates (B.Pharm / M.Pharm / Pharm.D / Life Sciences)
• Current Employer Appointment Letter & Recent Increment Letter
• Last 3 Months' Pay Slips & Bank Statements
• Government Photo ID Proof (Aadhaar Card and PAN Card)

📩 Direct E-mail Application Channel

Qualified Pharmacovigilance professionals can submit their updated CV directly to the Dr. Reddy’s Global Safety Talent Acquisition Desk:

• 📧 Direct HR Email: pv.careers@drreddys.com
• 📌 Subject Line Format: Application for PV - [ICSR/Aggregate Reporting] - [Years of Exp] - [Current Location] - [Your Name]
  • Example: Application for PV Specialist - ICSR Argus - 4 Years - Hyderabad - Sumanth Rao