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

15+ years
Not Disclosed
10 Jan. 31, 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

📌 Sr. Manager- R&D Quality (PV-QA) | Sun Pharmaceutical Industries Ltd - Gurgaon, Office
📍 Location: Gurgaon, India
💼 Company: Sun Pharmaceutical Industries Ltd
🕒 Experience: 15+ years

Role Overview

The Sr. Manager- R&D Quality (PV-QA) will oversee the quality assurance program for Pharmacovigilance (PV) at Sun Pharmaceutical. This position involves auditing, regulatory compliance, CAPA management, system validations, and ensuring alignment with global and regional regulatory requirements in pharmacovigilance operations.

Key Responsibilities

Quality Assurance Implementation: Develop and execute a comprehensive Quality Assurance program in alignment with global regulatory requirements, SOPs, and Sun Pharma policies.
Audit Program Development: Assist in the development of global Pharmacovigilance auditing programs, conduct audits for both Sun Pharma sites and outsourced vendors, CROs, and partners.
Audit Reporting & CAPA Management: Lead audits, report findings, manage CAPA (Corrective and Preventive Actions), and ensure they are effectively addressed and closed.
Harmonization of Quality Systems: Facilitate the consistent implementation of quality systems across Pharmacovigilance operations globally.
Internal Audit Database Management: Maintain and manage the Internal Audit Observation Database (IAOD), sharing audit reports, CAPA reports, and observations globally.
SOP Review & Compliance: Review Pharmacovigilance SOPs for completeness, clarity, and regulatory compliance.
Training & Mentorship: Conduct training on quality assurance procedures for Pharmacovigilance teams and new hires.
Inspection Readiness: Ensure Sun Pharma PV sites are always inspection-ready, including managing Corrective Actions and Preventive Actions (CAPA) for regulatory audits.
Computerized Systems Quality: Ensure compliance of GxP computerized systems at the R&D Gurugram (PVG) site and oversee system validations and quality standards.
Documentation & Risk Management: Oversee the Computerized System Validation Master Plan (CSVMP), manage documentation, and track remediation of system risks/gaps.
Cross-functional Collaboration: Work with various internal teams (e.g., Operations, Audit, R&D Quality) to ensure alignment and adherence to quality standards.
Global Communication: Liaise with internal teams and global regulatory bodies to ensure compliance and readiness for inspections.

Qualifications

🎓 Education:

  • Post Graduate in Pharmacy (M. Pharma) or Pharmacology.

💼 Experience:

  • 15+ years of experience in the Pharmacovigilance and Quality Assurance fields, including auditing, CAPA management, and system validations.

Desired Skills

  • Auditing skills with expertise in Pharmacovigilance.
  • Strong written and verbal English communication skills.
  • People management capabilities to train and supervise cross-functional teams.
  • Experience working with GxP Computerized Systems and ensuring regulatory compliance.
  • Ability to liaise with different teams and manage external vendors, CROs, and partners.

Benefits & Work Conditions

  • Full-time position based in Gurgaon, India.
  • Competitive salary and benefits package.
  • Travel may be required for inspections and audits.

📩 Apply Now