Navitas Life Sciences is a leading global provider of pharmacovigilance, regulatory, and clinical research services. With a strong commitment to quality and compliance, Navitas helps pharmaceutical and biotech companies navigate complex regulatory landscapes. The company is known for its expertise in Pharmacovigilance (PV), GVP compliance, and risk management, ensuring drug safety and patient well-being.
Job Title: QA Auditor (PV) / Sr. QA Auditor (PV)
Location: Bangalore / Chennai
Experience: 3+ years in Pharmacovigilance (PV)
Education: B.Pharm / M.Pharm / BDS / MSc (Life Sciences) or higher
Key Skills & Experience Required:
✔ 3+ years in Pharmacovigilance (PV) with strong knowledge of GVP guidelines
✔ 2+ years in conducting PV audits and managing PV Quality Management Systems (QMS)
✔ Alternative Experience:
- 5+ years in Global PV System management (Pharma/PV service providers)
- 3+ years in GCP/GVP audits
✔ Experience in CAPA Management (Corrective & Preventive Actions)
Job Description & Responsibilities:
- Implement and maintain Pharmacovigilance Quality Systems and compliance metrics.
- Conduct internal and external PV audits (projects, vendors, processes).
- Support customer audits and regulatory inspections (e.g., EMA, FDA).
- Investigate SOP deviations, quality issues, and complaints to determine root causes.
- Develop and track CAPA plans to ensure continuous improvement in PV processes.
- Ensure compliance with ICH-GCP, GVP, and global pharmacovigilance regulations.
Why Join Navitas Life Sciences?
✅ Work with a globally recognized PV and regulatory expert
✅ Opportunities for career growth in pharmacovigilance and compliance
✅ Collaborative work environment with industry-leading professionals
How to Apply?
Interested candidates can share their updated CV to:
📧 recruitment.bangalore@navitaslifesciences.com
