Dr. Reddy’s Laboratories is a global pharmaceutical leader committed to accelerating access to affordable and innovative medicines. Founded in 1984, the company now operates in 66 countries with 24,000+ employees, focusing on deep science, sustainability, and patient-centric healthcare.
With R&D centers, manufacturing facilities, and a strong commercial presence, Dr. Reddy’s aims to serve 1.5 billion+ patients by 2030. The company fosters an inclusive, diverse, and equal-opportunity workplace, ensuring a progressive and purpose-driven culture.
🔗 Official Website: www.drreddys.com
Job Description
Key Responsibilities:
✅ Signal Management: Conduct signal detection, review alerts, and ensure timely assessments.
✅ Aggregate Reports & RMPs: Prepare PSURs, PBRERs, DSURs, PADERs, and Risk Management Plans (RMPs).
✅ Regulatory & Clinical Support: Provide safety inputs for clinical study protocols, CRFs, SAPs, and labeling documents.
✅ Benefit-Risk Evaluation: Assist PV physicians in risk assessment and mitigation strategies.
✅ Regulatory Queries: Handle responses to health authority queries and ensure compliance.
✅ Process Improvement: Contribute to SOP updates, CAPA implementation, and digital transformation in PV.
Desired Skills & Qualifications:
✔ Education: M.Pharm (Pharmacology) or equivalent.
✔ Experience: 3-7 years in Pharmacovigilance & Medical Writing.
✔ Technical Skills: Strong knowledge of FDA, EU PV regulations, MS Office, and safety databases.
✔ Soft Skills: Excellent report writing, data analysis, teamwork, and time management.
Why Join Dr. Reddy’s?
- 🌍 Global Impact: Work on life-saving medicines for patients worldwide.
- 📈 Career Growth: Personalized learning & development programs.
- 💼 Employee Benefits:
- Medical & life insurance for family
- Maternity & paternity support
- Relocation assistance
- 🏦 Inclusive Culture: Equal opportunity employer with a focus on diversity.
🔗 Explore Careers: Dr. Reddy’s Careers
How to Apply?
