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Qa Auditor – Pv

3-5 years
Not Disclosed
10 June 13, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

QA Auditor – PV

Location: India
Work Mode: Not Specified (Assumed On-site or Hybrid)

Job Summary

We are looking for an experienced QA Auditor – PV to join our growing pharmacovigilance team. The ideal candidate will play a key role in ensuring compliance with global PV regulations and maintaining a robust Quality Management System. This position is perfect for professionals with a solid background in GVP audits, PV System Management, and CAPA handling, offering a challenging opportunity to contribute to critical drug safety and quality processes in the pharmaceutical industry.


Key Responsibilities

  • Implement and maintain the Pharmacovigilance (PV) system and quality processes.

  • Develop and monitor quality metrics related to PV activities.

  • Conduct audits of PV projects, systems, processes, and vendors.

  • Support the preparation and hosting of customer audits and PV inspections.

  • Ensure compliance with global PV and GVP guidelines across activities.


Required Skills & Qualifications

  • Minimum 5+ years of experience in Global PV System Management within pharmaceutical companies or PV service providers.

  • At least 3+ years of experience conducting GVP and GCP audits.

  • Strong understanding and application of Good Pharmacovigilance Practices (GVP) guidelines.

  • Proven experience in Corrective and Preventive Actions (CAPA) Management.

  • Minimum 3+ years of PV Quality Management System oversight.

  • Excellent attention to detail and understanding of global regulatory requirements.


Perks & Benefits

  • Competitive salary package (not specified in description).

  • Exposure to global PV systems and audit processes.

  • Opportunity to work with leading pharmaceutical clients and global quality teams.

  • Structured career development in pharmacovigilance and quality auditing.


Company Description

Join a globally recognized organization committed to pharmaceutical quality, drug safety, and regulatory excellence. The company is known for its strong presence in pharmacovigilance and offers a dynamic environment for QA professionals to contribute to meaningful healthcare outcomes.


Work Mode

Not explicitly mentioned (likely On-site or Hybrid based on role nature).


Call-to-Action

Ready to elevate your career in pharmacovigilance quality auditing? Apply now to become a key contributor in ensuring global drug safety and compliance.