Wipro Limited (NYSE: WIT) is a leading global IT, consulting, and business process services company. With a strong presence inย pharmaceutical and life sciences, Wipro delivers innovative solutions inย drug safety, clinical research, and regulatory compliance.
Job Details
- Role:ย Pharmacovigilance Quality Assurance Specialist
- Location:ย Pune (Work From Office)
- Shift:ย General Shift
- Experience:ย 3-6 Years
- Qualification:ย PhD / Pharm D / M.Pharm / B.Pharm / BDS / B.Tech/M.Tech (Life Sciences), M.Sc./B.Sc. (Life Sciences)
Key Skills Required
โ Strong knowledge of GVP (Good Pharmacovigilance Practices)
โ Experience in audits, compliance, and quality management in PV/Drug R&D
โ Candidates with ICSR case processing & QA in GMP/manufacturing may apply
Job Responsibilities
- Maintain trackers & prepare periodic metricsย for stakeholders.
- Ensure complianceย with SOPs for controlled documents.
- Review deviations & CAPAsย (Corrective and Preventive Actions).
- Manage training recordsย (induction, on-job, refresher training).
- Coordinate with internal teamsย for audits & inspections.
- Stay updatedย on regulatory guidelines (EMA, FDA, etc.).
- Support internal auditsย & external inspections.
- Document meeting minutesย and share updates.
Eligibility Criteria
- Education:ย Life Sciences/Pharmacy/Medical Graduates
- Experience:ย 3+ years inย Pharmacovigilance QA / Drug R&D
- Preferred:ย Knowledge ofย GxP (GMP, GLP, GCP)
Why Join Wipro?
โ
Global exposure in pharmaceutical compliance
โ
Stable career growth in a reputed IT & consulting firm
โ
Work-life balance with general shift timings
โ
Competitive salary & benefits
How to Apply?
๐ฉ Send your resume to: varsha.kamalapurkar@wipro.com
๐ Location: Pune (Work From Office)