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Qa Pharmacovigilance Executive – Drug Safety & Pv Quality Assurance

Sun Pharma
Sun Pharma
2+ years
Not Disclosed
Gurgaon, India
2 May 11, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill

QA Pharmacovigilance Executive – Drug Safety & PV Quality Assurance

Company: Sun Pharmaceutical Industries Ltd
Location: Gurgaon, Haryana, India
Work Mode: Office-Based
Department: R&D – Quality – Pharmacovigilance QA
Job Grade: Executive


About the Opportunity

Sun Pharmaceutical Industries Ltd is hiring a QA Pharmacovigilance Executive for its Pharmacovigilance Quality Assurance division in Gurgaon. This role is ideal for professionals with experience in Pharmacovigilance Quality Assurance (PVQA), Drug Safety Audits, Signal Management, PSUR activities, and Regulatory Compliance.

The selected candidate will support global pharmacovigilance quality systems, audit programs, CAPA management, SOP compliance, and vendor quality oversight while collaborating with cross-functional global teams.

This opportunity is best suited for candidates with approximately 2 years of experience in Pharmacovigilance Quality Assurance, PSUR, or Signal Management.


Key Responsibilities

Pharmacovigilance Quality Assurance Activities

  • Assist in developing and maintaining the global Pharmacovigilance auditing program
  • Conduct and report audits as a Lead Auditor or Co-Auditor for:
    • CROs
    • Service Providers
    • Vendors
    • Affiliates and Business Partners
  • Support audits for Sun Pharma sites associated with Pharmacovigilance operations
  • Ensure compliance with established quality systems and global pharmacovigilance standards

Audit & CAPA Management

  • Manage the Internal Audit Observation Database (IAOD)
  • Share audit reports, CAPA reports, and global observations with regional PV teams
  • Ensure CAPAs are properly addressed, tracked, and closed within timelines
  • Review and close deviations raised at global and regional levels
  • Monitor effectiveness of corrective and preventive actions

SOP & Documentation Management

  • Review Pharmacovigilance SOPs for:
    • Clarity
    • Completeness
    • Regulatory compliance
  • Prepare and update departmental SOPs
  • Maintain quality documentation and records in line with regulatory standards
  • Support Learning Management System (LMS) activities and training record management

Regulatory & Compliance Support

  • Assist operations teams during:
    • Corporate audits
    • External inspections
    • Regulatory assessments
  • Collaborate with cross-functional departments to maintain pharmacovigilance quality standards
  • Participate in global quality initiatives and action tracking activities
  • Support R&D Quality System activities assigned by management

Educational Qualification

Candidates should possess any of the following qualifications:

  • M.Pharm (Master of Pharmacy)
    OR
  • BDS (Bachelor of Dental Surgery)

Required Experience

  • Around 2 years of experience in:
    • Pharmacovigilance Quality Assurance (PVQA)
    • PSUR Management
    • Signal Management
    • Drug Safety Compliance
    • Regulatory Quality Systems

Suitable For

  • Experienced Pharmacovigilance professionals
  • Candidates with exposure to PV audits and quality systems
  • Professionals seeking growth in global drug safety quality operations