🚨 Pharmacovigilance Quality Assurance Specialist
- 🏢 Company: Wipro
- 📍 Location: Pune (Work From Office)
- 🎓 Eligibility: PhD / Pharm D / M.Pharm / B.Pharm / BDS / B.Tech/M.Tech (Life Sciences), M.Sc./B.Sc. (Life Sciences)
- 🧪 Experience: 3-6 Years
- 📝 Job Type: Full-Time | PV Quality Assurance
- 🔎 Verified: ✅ Verified Opportunity
🧬 About Company
Wipro Limited (NYSE: WIT) is a global IT, consulting, and business process services company. With a strong presence in pharmaceutical and life sciences sectors, Wipro delivers cutting-edge solutions in drug safety, regulatory compliance, and clinical development services for global clients.
📄 Job Overview
Job Title: Pharmacovigilance Quality Assurance Specialist
Location: Pune (WFO)
Shift: General Shift
Application Mode: Email Application
🧑💼 Key Responsibilities
- Maintain trackers and prepare periodic metrics for stakeholders.
- Ensure compliance with SOPs for controlled documents.
- Review deviations and implement Corrective and Preventive Actions (CAPAs).
- Maintain training records including induction, on-job, and refresher trainings.
- Coordinate audits and inspections with internal teams.
- Stay up-to-date with global regulatory guidelines (EMA, FDA, etc.).
- Support internal audits and external inspections.
- Document meeting minutes and share with stakeholders.
✅ Required Skills & Qualifications
- Degree in Life Sciences / Pharmacy / Medical stream (B.Pharm, M.Pharm, Pharm D, PhD, BDS, M.Sc.).
- 3+ years of experience in PVQA / Drug R&D.
- Strong understanding of GVP (Good Pharmacovigilance Practices).
- Familiarity with ICSR case processing is an added advantage.
- Knowledge of GxP environments (GMP, GLP, GCP) is preferred.
🎯 Why Join Wipro?
- 🌍 Work with global pharma & biotech clients.
- 📈 Career growth within a trusted IT & consulting leader.
- 🕐 Work-life balance with general shift schedule.
- 💼 Competitive salary, benefits, and learning resources.
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Tags: Wipro PVQA Jobs, Pharmacovigilance Quality Jobs, Pharma Compliance Jobs Pune, Medical QA Jobs, Apply Wipro Pharmacovigilance 2025
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