Wipro Limited (NYSE: WIT) is a leading global IT, consulting, and business process services company. With a strong presence in pharmaceutical and life sciences, Wipro delivers innovative solutions in drug safety, clinical research, and regulatory compliance.
Job Details
- Role: Pharmacovigilance Quality Assurance Specialist
- Location: Pune (Work From Office)
- Shift: General Shift
- Experience: 3-6 Years
- Qualification: PhD / Pharm D / M.Pharm / B.Pharm / BDS / B.Tech/M.Tech (Life Sciences), M.Sc./B.Sc. (Life Sciences)
Key Skills Required
✔ Strong knowledge of GVP (Good Pharmacovigilance Practices)
✔ Experience in audits, compliance, and quality management in PV/Drug R&D
✔ Candidates with ICSR case processing & QA in GMP/manufacturing may apply
Job Responsibilities
- Maintain trackers & prepare periodic metrics for stakeholders.
- Ensure compliance with SOPs for controlled documents.
- Review deviations & CAPAs (Corrective and Preventive Actions).
- Manage training records (induction, on-job, refresher training).
- Coordinate with internal teams for audits & inspections.
- Stay updated on regulatory guidelines (EMA, FDA, etc.).
- Support internal audits & external inspections.
- Document meeting minutes and share updates.
Eligibility Criteria
- Education: Life Sciences/Pharmacy/Medical Graduates
- Experience: 3+ years in Pharmacovigilance QA / Drug R&D
- Preferred: Knowledge of GxP (GMP, GLP, GCP)
Why Join Wipro?
✅ Global exposure in pharmaceutical compliance
✅ Stable career growth in a reputed IT & consulting firm
✅ Work-life balance with general shift timings
✅ Competitive salary & benefits
How to Apply?
📩 Send your resume to: varsha.kamalapurkar@wipro.com
📍 Location: Pune (Work From Office)
