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Navatio Pharma Solutions is inviting applications for the role of Quality Assurance Pharmacovigilance (PV) Specialist. This is a remarkable opportunity for professionals passionate about patient safety and regulatory excellence to contribute meaningfully in a dynamic and growing organization.
📌 Job Details
- Position: Quality Assurance Pharmacovigilance (PV) Specialist
- Location: Hyderabad, India
- Job Type: Full-Time
- Availability: Immediate Joiners Preferred
📝 Position Summary
The selected candidate will ensure the highest standards in pharmacovigilance services, focusing on compliance, quality management, and regulatory alignment. This role plays a key part in maintaining and improving PV quality systems for both internal teams and external clients.
🔍 Key Responsibilities
- Provide QA oversight across PV activities such as AE reporting, signal detection, and risk management
- Plan and conduct internal/external audits ensuring compliance with GVP and global regulations
- Review safety documents for completeness, accuracy, and compliance
- Monitor adherence to international regulatory frameworks (FDA, EMA, ICH, WHO)
- Lead CAPA implementation for identified quality gaps
- Deliver PV-related QA training to internal teams and clients
- Stay abreast of industry trends and regulatory updates to recommend process enhancements
- Collaborate with cross-functional teams to align quality across PV workflows
- Act as the main QA contact for clients on PV compliance matters
🎓 Eligibility Criteria
- Education: Bachelor’s or Master’s in Life Sciences, Pharmacy, Medicine, or related field
- Experience:
- 3–5 years total experience in Pharmacovigilance
- Minimum 2 years in a QA or audit-focused PV role within pharmaceutical/CRO industry
📩 How to Apply
Interested candidates can share their updated CVs at:
📧 hr@navatiopharma.com
