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.
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