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Sr. Manager- R&D Quality (Pv-Qa)

15+ years
Not Disclosed
10 April 30, 2025
Job Description
Job Type: Full Time Education: M.Pharm 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

 

Title: Sr. Manager – R&D Quality (PV-QA)
Date Posted: April 25, 2025
Location: Gurgaon – Office
Company: Sun Pharmaceutical Industries Ltd


Job Overview:

Sun Pharma is seeking a Senior Manager in R&D Quality (GPvP QA) for its Pharmacovigilance Quality Assurance team based in Gurgaon. This strategic leadership role focuses on ensuring the implementation of global QA programs, regulatory compliance, auditing, and quality system governance within pharmacovigilance operations and computerized systems.


Department: R&D Quality (GPvP QA)

Designation: Senior Manager
Location: Gurgaon


Key Responsibilities:

  • Implement and maintain a documented QA program compliant with global and regional pharmacovigilance regulations.

  • Lead and conduct audits (Sun Pharma sites, CROs, vendors, affiliates, and partners) to ensure PV quality compliance.

  • Manage the Internal Audit Observation Database (IAOD) and CAPA lifecycle.

  • Harmonize and implement quality systems and SOPs across PV functions.

  • Conduct Quality Review Board (QRB) meetings for PV.

  • Prepare monthly QA performance reports for submission to the R&D Quality Head.

  • Ensure regulatory inspection readiness across all Sun Pharma PV sites and drive CAPA implementation post-inspections.

  • Conduct PV procedural and induction trainings for QA and operations personnel.

  • Oversee and ensure compliance of GxP Computerized Systems at the R&D Gurgaon site.

  • Serve as Process Quality Lead (PQL) for validation of computerized systems.

  • Review and manage system documentation: CSVMPs, system inventory, deviation logs, change controls, and periodic quality activities.

  • Support corporate audits and participate in remediation tracking and risk management for computerized systems.

  • Perform additional responsibilities as assigned by R&D Quality leadership.


Education and Experience:

  • Postgraduate in Pharmacy (M. Pharm) or Pharmacology

  • Approximately 15 years of relevant experience in Pharmacovigilance QA and R&D Quality functions


Technical & Behavioral Competencies:

  • Strong auditing and documentation skills

  • Effective verbal and written communication in English

  • Leadership and people management capabilities

  • Strong cross-functional collaboration and stakeholder liaison skills