Navatio Pharma Solutions – Hiring Quality Assurance Pharmacovigilance (PV) Specialist |

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.

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📌 Job Details

• Position: Quality Assurance Pharmacovigilance (PV) Specialist
• Location: Hyderabad, India
• Job Type: Full-Time
• Availability: Immediate Joiners Preferred

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📝 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.

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🔍 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

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🎓 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

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📩 How to Apply

Interested candidates can share their updated CVs at:
📧 hr@navatiopharma.com