Global pharmaceutical leader Novo Nordisk has announced a new opportunity for experienced pharmacovigilance professionals. The company is hiring a PV Compliance Specialist, QPPV Office for its Global Patient Safety team in Bangalore, Karnataka. Candidates with a Master’s degree in Life Sciences and significant experience in pharmacovigilance, PV audits, inspections, compliance, and quality management systems are encouraged to apply.
This is an excellent opportunity to join one of the world’s most respected healthcare organizations and contribute to global patient safety, regulatory compliance, and pharmacovigilance excellence.
Job Overview
| Details | Information |
|---|---|
| Position | PV Compliance Specialist, QPPV Office |
| Company | Novo Nordisk |
| Department | Global Patient Safety (GPS) |
| Category | Regulatory Affairs & Safety Pharmacovigilance |
| Location | Bangalore, Karnataka, India |
| Experience Required | 5+ Years |
| Qualification | Master’s Degree in Life Sciences |
| Application Deadline | 21 June 2026 |
| Employment Type | Full-Time |
Key Responsibilities
The selected candidate will support the QPPV Office and Pharmacovigilance Excellence team through various compliance and quality management activities.
QPPV Office Coordination
- Coordinate QPPV Office activities and oversight meetings.
- Collect and analyze compliance metrics and safety data.
- Support preparation and maintenance of global and local Pharmacovigilance System Master Files (PSMFs).
Pharmacovigilance Quality Management
- Develop and monitor PV Quality Management System (QMS) activities.
- Support implementation of pharmacovigilance KPIs and SOPs.
- Contribute to risk management and compliance reporting initiatives.
Deviation and CAPA Management
- Manage deviations and corrective and preventive actions (CAPAs).
- Act as Deviation Owner and Change Request Owner when required.
- Ensure timely follow-up and resolution of compliance issues.
PV Audits and Inspections
- Support headquarters pharmacovigilance audits and regulatory inspections.
- Coordinate inspection readiness activities and stakeholder training.
- Assist with inspection responses, CAPA tracking, and report distribution.
Compliance Analysis and Reporting
- Perform trend analysis of pharmacovigilance findings.
- Provide compliance insights for PSMF updates.
- Communicate audit and inspection outcomes to process owners.
Training and Continuous Improvement
- Deliver pharmacovigilance compliance training.
- Support global affiliates and headquarters teams.
- Monitor evolving PV regulations and industry best practices.
Required Qualifications
Candidates applying for this pharmacovigilance compliance job should possess:
Educational Qualification
- Master’s Degree in Life Sciences or related discipline.
Experience
- Minimum 5 years of experience in Pharmacovigilance.
- Experience across multiple PV functions.
- Hands-on exposure to PV audits and inspections.
Technical Skills
- Strong understanding of pharmacovigilance regulations.
- Knowledge of global drug safety requirements.
- Familiarity with GCP and GxP documentation.
- Experience with PV quality metrics and compliance KPIs.
- Proficiency in pharmaceutical industry IT systems.
Professional Skills
- Excellent analytical and problem-solving abilities.
- Strong project coordination skills.
- Ability to manage multiple priorities and deadlines.
- Effective communication and stakeholder management skills.
- Experience working in global cross-functional teams.
Language Requirement
- Excellent written and spoken English.
Why Join Novo Nordisk?
Novo Nordisk is recognized globally for its commitment to innovation, patient safety, and healthcare transformation.
Employee Benefits
- Opportunity to work with a leading global pharmaceutical company.
- Exposure to international pharmacovigilance operations.
- Collaborative global work environment.
- Career growth and professional development opportunities.
- Participation in global compliance and inspection readiness programs.
- Opportunity to contribute directly to patient safety initiatives worldwide.
About the Department
The QPPV Office & PV Excellence team within Global Patient Safety (GPS) ensures the highest standards of pharmacovigilance compliance across Novo Nordisk’s worldwide operations. The team collaborates closely with colleagues in Denmark, India, the United States, and global affiliates to maintain inspection readiness and regulatory compliance.
How to Apply
