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Pv Compliance Specialist, Qppv Office

Novo Nordisk
5+ years
INR 22 LPA – 35 LPA
Bangalore, India
1 June 10, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, 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, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding

PV Compliance Specialist – 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 seeking an experienced PV Compliance Specialist to join the QPPV Office & PV Excellence Team within Global Patient Safety.

This role is responsible for supporting pharmacovigilance (PV) compliance oversight, quality management systems, audit and inspection readiness, QPPV Office coordination, and continuous improvement of global PV processes. The successful candidate will work closely with the EU Qualified Person for Pharmacovigilance (QPPV), PV Excellence leadership, and global affiliates to ensure compliance with international pharmacovigilance regulations and quality standards.

This position is ideal for professionals with strong expertise in pharmacovigilance compliance, quality systems, audits, inspections, CAPA management, and regulatory oversight.


Key Responsibilities

QPPV Office Coordination

  • Coordinate QPPV Office activities across global and affiliate functions.

  • Schedule and facilitate QPPV Oversight Meetings.

  • Compile and analyze compliance metrics and safety data.

  • Support preparation and maintenance of:

    • Global Pharmacovigilance System Master Files (PSMFs)

    • Local Pharmacovigilance System Master Files (PSMFs)

  • Ensure accurate and timely documentation of compliance activities.

Pharmacovigilance Quality Management System (PV-QMS)

  • Support development, implementation, and maintenance of PV Quality Management Systems.

  • Develop and monitor:

    • Quality KPIs

    • Compliance Metrics

    • Performance Indicators

  • Contribute to Risk & Compliance Committee activities.

  • Support quality governance and oversight processes.

Deviation & CAPA Management

  • Manage pharmacovigilance deviations and quality events.

  • Act as:

    • Deviation Owner

    • Change Request Owner

  • Ensure timely investigation, documentation, and closure of deviations.

  • Track Corrective and Preventive Actions (CAPAs).

  • Monitor effectiveness of implemented CAPAs.

Compliance Monitoring & Trend Analysis

  • Perform trending and analysis of:

    • Audit Findings

    • Inspection Findings

    • Compliance Deviations

    • Quality Metrics

  • Identify systemic risks and improvement opportunities.

  • Provide compliance insights to process owners and leadership teams.

  • Contribute compliance findings to PSMF documentation.

PV Audits & Inspection Readiness

  • Support the Inspection Responsible function for:

    • Health Authority Inspections

    • Internal Audits

    • External Audits

  • Coordinate inspection preparation activities.

  • Support:

    • Inspection Rehearsals

    • Stakeholder Training

    • Inspection Room Setup

    • Pre-Inspection Requests

  • Assist during on-site and virtual inspections.

Health Authority Inspection Support

  • Coordinate responses to inspection findings.

  • Support preparation of inspection responses.

  • Track CAPA implementation following inspections.

  • Ensure timely communication of inspection outcomes.

  • Maintain inspection-related documentation.

Training & Stakeholder Support

  • Deliver PV compliance and inspection-readiness training.

  • Act as Subject Matter Expert (SME) for:

    • PV Audits

    • PV Inspections

    • Compliance Processes

  • Support affiliates and headquarters teams with PV compliance guidance.

Process Improvement & Regulatory Intelligence

  • Monitor evolving global pharmacovigilance regulations.

  • Evaluate industry best practices and compliance trends.

  • Contribute to continuous improvement of:

    • PV Processes

    • SOPs

    • Compliance Frameworks

    • Digital Solutions

  • Support innovation and operational excellence initiatives.


About the Department

The QPPV Office & PV Excellence Team is part of Novo Nordisk's Global Patient Safety organization.

The team collaborates closely with:

  • Global Patient Safety (GPS)

  • EU QPPV Office

  • Denmark Headquarters

  • GPS Bangalore

  • GPS USA

  • Global Affiliates

The department ensures robust pharmacovigilance oversight, inspection readiness, compliance excellence, and quality governance across the Novo Nordisk global safety system.


Required Qualifications

Education

  • Master's Degree in:

    • Pharmacy (M.Pharm)

    • Pharmacology

    • Life Sciences

    • Biotechnology

    • Biological Sciences

    • Related Healthcare Discipline

Preferred

  • Additional certification in:

    • Pharmacovigilance

    • Quality Management

    • Regulatory Affairs

    • GxP Compliance


Experience

  • Minimum 5+ years of experience in Pharmacovigilance.

  • Experience in:

    • PV Compliance

    • Drug Safety Operations

    • PV Audits

    • Regulatory Inspections

    • Quality Systems

    • CAPA Management

    • PSMF Management