Novo Nordisk Require PV Proc Excellence Principal Specialist

Novo Nordisk is a global healthcare company with 89 years of innovation and leadership in diabetes care. The company also has leading positions within Haemophilia care, growth hormone therapy and hormone replacement therapy.

Post : Principal Specialist, PV Proc Excellence

As Principal Specialist, PV Process Excellence, you will strengthen the governance and continuous improvement of Novo Nordisk's global pharmacovigilance processes. You will translate emerging regulatory requirements into sustainable, compliant and inspection-ready ways of working, and help keep our patient safety system effective at scale. Your work supports the integrity of the system that protects people who rely on our medicines every day.

Job Description
• Facilitate the regulatory intelligence and process governance boards, deputising for the Chair when required, and ensure the frameworks run with operational rigour and efficiency.
• Drive systematic surveillance and assessment of emerging pharmacovigilance regulations, guidelines and best practices, and translate them into actionable organisational requirements.
• Maintain oversight of global and local regulatory changes impacting the pharmacovigilance system, and manage the impact of process changes across it.
• Advance the maturity and inspection readiness of pharmacovigilance processes, standards and procedures, harmonising global procedures with functional stake-holders.
• Support the global training governance framework, shaping GPS training curricula, role-based learning, effec-tiveness measurement and compliance monitoring.
• Take primary ownership of specific procedural documentation for the PV Process Excellence team.

Candidate Profile
• A Bachelor's degree in life sciences or a related field, combined with 5–10 years' relevant pharmacovigilance experience.
• Significant experience within pharmacovigilance operations, quality systems, governance, compliance or QPPV Office functions.
• A strong understanding of worldwide pharmacovigilance regulation and the ability to translate requirements into pragmatic, high-quality execution.
• Experience in pharmacovigilance regulatory intelligence, process governance and training will be a an added advantage
• Demonstrated ability to provide strategic planning, governance and oversight across multiple large-scale, com-plex assignments.
• Strong communication and stakeholder-management skills.
• A team-oriented mindset with flexibility, change readiness and a drive to simplify while maintaining compliance.
• Fluency in English, both written and spoken.

Additional Information
Experience : 5–10 years
Qualification : PV Proc Excellence
Location : Bangalore, Karnataka
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : PV Proc Excellence
End Date : 20th October 2026