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