Novo Nordisk is hiring 2 PV Process Excellence Specialists for its Global Patient Safety (GPS) team at Novo Nordisk Global Business Services (GBS), Bangalore, Karnataka.

This opportunity is suited to professionals with 5+ years of pharmacovigilance experience and backgrounds in PV operations, quality systems, governance, compliance, regulatory intelligence, process excellence, or QPPV Office functions.

Job Details

About the PV Process Excellence Specialist Role

The selected professionals will support global pharmacovigilance process governance and continuous improvement. The role works closely with the Director of PV Process Excellence, EU QPPV, Deputy QPPVs, Global Patient Safety leadership and other cross-functional stakeholders.

The position is particularly focused on PV regulatory intelligence, process governance, inspection readiness, procedural documentation and organisational training.

This makes the role relevant for experienced pharmacovigilance professionals looking to move beyond case-processing operations into PV quality, governance and process excellence.

Key Responsibilities

As a PV Process Excellence Specialist, responsibilities may include:

• Coordinate logistics for global pharmacovigilance governance boards.
• Prepare agendas, schedule meetings, document minutes and track action items.
• Monitor emerging pharmacovigilance regulations, guidelines and industry best practices.
• Support regulatory intelligence surveillance and assessment activities.
• Contribute to the maturity and inspection readiness of PV processes, standards and procedures.
• Oversee completeness of PV impact assessments.
• Support training completeness and timely completion across the pharmacovigilance system.
• Maintain inspection readiness of pharmacovigilance training records.
• Support ownership of selected procedural documentation.
• Contribute to continuous improvement of global PV processes and ways of working.
• Work with global stakeholders across GPS, R&D, affiliates, health authorities and contractual partners.

Novo Nordisk PV Job Eligibility

Candidates applying for this Novo Nordisk pharmacovigilance job in Bangalore should have:

• A Bachelor’s degree in Life Sciences and/or Pharmaceutical Sciences.
• At least 5 years of relevant pharmacovigilance experience.
• Experience in pharmacovigilance operations, quality systems, governance, compliance or QPPV Office functions.
• Understanding of worldwide pharmacovigilance regulations.
• Ability to interpret regulatory requirements and translate them into practical processes.
• Experience with strategic planning, governance and oversight of complex assignments.
• Strong communication and stakeholder-management skills.
• Strong written and spoken English.
• A structured and detail-oriented approach to work.
• Ability to work effectively in a global and cross-functional environment.

Preferred Experience

Experience in any of the following areas can be particularly relevant to the position:

PV Regulatory Intelligence | Process Governance | PV Quality Systems | QPPV Office | Inspection Readiness | PV Training | Compliance | Process Excellence

Why This Role Is Relevant for Experienced PV Professionals

Unlike roles focused primarily on individual case processing, this position involves pharmacovigilance governance, regulatory intelligence, quality-system oversight and process improvement at a global level.

The role is part of the QPPV Office within Global Patient Safety, providing exposure to global PV governance and collaboration with multiple stakeholders across the organisation.

Location

Novo Nordisk Global Business Services (GBS)
Bangalore, Karnataka, India

Application Deadline

The application deadline mentioned in the job posting is:

29 September 2026

Candidates interested in this opportunity should submit their application through the official Novo Nordisk careers channel before the deadline.

How to Apply

Application Link 1

Application Link 2