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Sr Pv Compliance Professional Qppv Off.

Novo Nordisk
3-5 years
INR 12 LPA – 22 LPA
Bangalore, India
1 June 10, 2026
Job Description
Job Type: Education: M.Pharm/B.Pharm or M.Sc. Skills: Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management

PV Compliance Senior Professional – QPPV Office

Company: Novo Nordisk Global Business Services (GBS)
Department: QPPV Office & PV Excellence, Global Patient Safety (GPS)
Location: Bangalore, Karnataka, India
Employment Type: Full-Time


About the Role

Novo Nordisk is looking for a highly motivated PV Compliance Senior Professional to join the QPPV Office & PV Excellence Team within Global Patient Safety.

This role supports pharmacovigilance compliance, quality management systems, PSMF maintenance, audit and inspection readiness, compliance reporting, and QPPV Office activities. The successful candidate will work closely with global stakeholders, ensuring compliance with international pharmacovigilance regulations and maintaining high-quality safety governance processes.

The position offers an excellent opportunity for professionals seeking to build expertise in global pharmacovigilance compliance, regulatory inspections, and quality excellence within a leading multinational pharmaceutical organization.


Key Responsibilities

QPPV Office Support

  • Provide operational and administrative support to the QPPV Office.

  • Coordinate and support QPPV Oversight Meetings.

  • Maintain meeting documentation, action trackers, and compliance records.

  • Support execution of global pharmacovigilance governance activities.

Pharmacovigilance System Master File (PSMF) Management

  • Support maintenance of:

    • Global PSMFs

    • Local PSMFs

  • Ensure timely updates to safety system documentation.

  • Coordinate collection of information from global stakeholders.

  • Support PSMF quality reviews and compliance checks.

Quality Management System (QMS) Support

  • Assist in implementation and maintenance of:

    • Pharmacovigilance SOPs

    • Work Instructions

    • Quality Management Processes

  • Support development and monitoring of Quality KPIs.

  • Contribute to compliance reporting and quality oversight activities.

Compliance Monitoring & Reporting

  • Compile and analyze Quality KPI data.

  • Prepare compliance dashboards and reports.

  • Monitor pharmacovigilance compliance metrics.

  • Support identification of process improvement opportunities.

Audit & Inspection Readiness

  • Support preparation for:

    • Health Authority Inspections

    • Internal Audits

    • External Audits

  • Assist in gathering documentation and evidence.

  • Participate in inspection readiness activities.

  • Support tracking of audit findings and follow-up actions.

Training & Knowledge Management

  • Deliver pharmacovigilance-related training when required.

  • Support training initiatives across headquarters and affiliate organizations.

  • Promote awareness of compliance requirements and quality standards.

  • Contribute to knowledge-sharing activities.

Cross-Functional Collaboration

  • Collaborate with:

    • Global Patient Safety Teams

    • Regulatory Affairs

    • Quality Assurance

    • Clinical Development

    • Legal & Compliance Functions

  • Support implementation of global compliance initiatives.

  • Participate in internal working groups and improvement projects.

Process Improvement & PV Excellence

  • Support optimization of pharmacovigilance quality frameworks.

  • Identify opportunities to enhance compliance processes.

  • Contribute to continuous improvement initiatives.

  • Assist in implementation of best practices across the organization.


About the Department

The QPPV Office & PV Excellence Team is part of Novo Nordisk's Global Patient Safety organization and is responsible for ensuring that the company's global pharmacovigilance system meets the highest standards of quality, compliance, and regulatory excellence.

The team works closely with:

  • Global Patient Safety

  • Regulatory Affairs

  • Quality Assurance

  • Legal & Compliance Teams

  • Health Authorities

  • Global Affiliates

to maintain a robust pharmacovigilance framework and support patient safety worldwide.


Required Qualifications

Education

  • Master's Degree in:

    • Pharmacy (M.Pharm)

    • Pharmacology

    • Life Sciences

    • Biotechnology

    • Biological Sciences

    • Related Healthcare Discipline

Preferred

  • Additional certification in:

    • Pharmacovigilance

    • Regulatory Affairs

    • Quality Management

    • GxP Compliance


Experience

  • 3–5 years of experience in:

    • Pharmacovigilance

    • Drug Safety

    • PV Compliance

    • Quality Systems

    • Regulatory Compliance

    • Safety Operations