Department: Regulatory Affairs, Research & Development
Location: Novo Nordisk Global Business Services (GBS), Bangalore
Your impact begins here
As Sr Regulatory Professional, you will lead the regulatory strategy that moves Novo products through development, approval and lifecycle management worldwide. You will own submissions and Health Authority interactions, shape core labelling that reflects what makes a product different, and represent Regulatory Affairs in the Global Project Team. Your decisions will help determine how quickly and clearly new treatments reach people living with serious chronic diseases, and how reliably they stay available.
What You’ll Bring
You are an experienced regulatory qualified who can set strategy, negotiate with Health Authorities and keep complex global projects moving. You will bring:
• A degree in Pharmacy (B.Pharm/M.Pharm/Life Science) or a related scientific discipline.
• 12–15+ years of experience in regulatory affairs or closely related areas across the pharmaceutical R&D; value chain.
• In-depth knowledge of regulatory science and requirements in the EU, US, China and Japan, as well as other regions, including hands-on submission experience in these markets.
• Proven experience in lifecycle management, label development, Health Authority interactions, device development and regulatory intelligence.
• Strong project management skills and the ability to simplify complex work for yourself and others.
• Strong negotiation, stakeholder management and networking skills, with the ability to build trust across functions and cultures.
• A thorough understanding of the therapy area, which you use to lead and guide decisions.
• Proficiency in written and spoken English.
You take personal leadership, adapt quickly when priorities change, spot problems early and make bold, well-founded decisions. You welcome honest feedback and enjoy helping others grow.
What You’ll Do
The role spans six ar
📌 Sr Regulatory Professional (Bengaluru)
🏢 Novo Nordisk
📍 Bengaluru
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