Dr. Reddy’s Laboratories Ltd. is a multinational pharmaceutical leader with a presence in 66+ countries. Founded in 1984, the company is committed to accelerating access to affordable and innovative medicines. With 24,000+ employees, Dr. Reddy’s focuses on deep science, sustainability, and corporate governance.
Key Highlights:
✔ Global footprint: R&D centers, manufacturing facilities, and commercial operations worldwide.
✔ Mission: Reach 1.5 billion+ patients by 2030 through innovation and sustainability.
✔ Work Culture: Inclusive, diverse, and driven by “Good Health Can’t Wait”.
Key Responsibilities:
- Update local and core PSMFs (Pharmacovigilance System Master Files).
- Manage SDEA (Safety Data Exchange Agreements) with partners.
- Ensure Eudravigilance database compliance and signal detection.
- Handle Risk Management Plans (RMPs) and CMDh risk notifications.
- Oversee aggregate reports (PSUSAs, PSURs) and regulatory tracking.
- Support audits, inspections, and CAPA (Corrective & Preventive Actions).
- Work with cross-functional global teams and vendors.
Skills & Competencies:
- Bachelor’s/Master’s in Pharmacy (preferred).
- 8+ years in Pharmacovigilance, with 3+ years in core pharma companies.
- Strong knowledge of EUG & ROW regulatory guidelines.
- Proficiency in Microsoft Office (Excel, PowerPoint).
- Excellent communication, multitasking, and organizational skills.
Why Join Dr. Reddy’s?
Benefits & Perks:
✅ Career Growth: Personalized learning & development programs.
✅ Health & Wellness: Medical & life insurance for employees & family.
✅ Work-Life Balance: Maternity/Paternity benefits, relocation support.
✅ Inclusive Culture: Equal opportunity employer with a diverse workforce.
Work Environment:
- Innovative & collaborative culture.
- Focus on sustainability and patient impact.
- Recognized by World Economic Forum for manufacturing excellence.
