Novo Nordisk, a global leader in pharmaceuticals and chronic disease management, is hiring a Regulatory Professional I for its International Operations Regulatory Affairs (IORA) team in Bangalore, Karnataka. This opportunity is ideal for experienced Regulatory Affairs professionals looking to work in a global affiliate and shared service model, supporting NDA submissions, lifecycle management, and international regulatory compliance.
If you have strong experience in regulatory submissions, health authority interactions, and product approvals across international markets, this role offers long-term growth in a high-impact global environment.
📌 Job Details
- Job Title: Regulatory Professional I
- Category: Regulatory Affairs & Safety Pharmacovigilance
- Location: Bangalore, Karnataka, India
- Team: International Operations Regulatory Affairs (IORA)
- Company: Novo Nordisk Global Business Services (GBS)
- Employment Type: Full-Time
- Application Deadline: 4 February 2026
🧾 Key Responsibilities (Regulatory Affairs)
As a Regulatory Professional at Novo Nordisk, you will be responsible for:
- Securing regulatory approvals for new products (NDA) and life cycle management (LCM) licenses across assigned countries
- Managing end-to-end regulatory submissions, including preparation and review of country-specific application forms
- Coordinating with distributors, affiliates, and health authorities (HA) to ensure compliance and timely approvals
- Reviewing regulatory documentation for tenders and authority submissions
- Maintaining and updating Veeva Vault Regulatory with dossier and approval data within defined timelines
- Supporting labelling development, review of promotional materials, and compliance with local regulations
- Monitoring local regulatory intelligence and ensuring continuous regulatory compliance
- Providing post-approval and regulatory signal support aligned with HA requirements
🎓 Qualifications & Experience Required
To be successful in this Regulatory Affairs job at Novo Nordisk, candidates should have:
- Postgraduate degree (or equivalent) in Science / Pharmacy / Life Sciences
- 5+ years of experience in Pharmaceutical Regulatory Affairs
- 3+ years of experience working with international stakeholders outside India
- Experience in an affiliate environment or shared service model (preferred)
- Proven experience in health authority interactions
- Working knowledge of global regulatory submissions and lifecycle activities
- Basic project management skills with ability to handle multiple priorities
🌍 About the Department – IORA Bangalore
The International Operations Regulatory Affairs – Bangalore (IORA) team is a strategic extension of Novo Nordisk’s global RA organization based in Zurich and Copenhagen. The department plays a critical role in enabling fast, high-quality product approvals, portfolio integration, and regulatory compliance across international markets.
💼 Why Work at Novo Nordisk?
- Work with a top global pharmaceutical company with 100+ years of legacy
- Exposure to global regulatory strategies and submissions
- Collaborative, inclusive, and purpose-driven work culture
- Opportunity to contribute to treatments for serious chronic diseases
- Long-term career growth in international regulatory affairs
