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Senior Regulatory Professional

Novo Nordisk
7-9 years
INR 25 LPA – 40 LPA
Bangalore, India
1 June 16, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs

Senior Regulatory Professional

Location: Bangalore, Karnataka, India
Employment Type: Full-Time
Company: Novo Nordisk Global Business Services (GBS)

Position Summary

The Senior Regulatory Professional is responsible for leading global regulatory strategy, regulatory submissions, health authority interactions, labeling management, lifecycle management activities, and regulatory due diligence for Novo Nordisk's Diabetes portfolio. The role serves as a Subject Matter Expert (SME) across multiple regulatory disciplines, ensuring successful product development, approvals, market expansion, and regulatory compliance across major global markets including the US, EU, China, and Japan.

Key Responsibilities

Global Regulatory Submissions

  • Develop and execute global Regulatory Affairs Submission Plans.

  • Prepare, review, publish, and maintain regulatory dossiers.

  • Lead regulatory submissions across global markets.

  • Manage submission timelines and regulatory deliverables.

  • Support product approvals and registration activities globally.

Regulatory Filing & Lifecycle Management

  • Manage and support:

    • MAA (Marketing Authorization Applications)

    • NDA (New Drug Applications)

    • BLA (Biologics License Applications)

    • CTA (Clinical Trial Applications)

    • IND (Investigational New Drug Applications)

    • PIP (Pediatric Investigation Plans)

    • PSP (Pediatric Study Plans)

    • DSUR

    • PSUR/PBRER

    • Risk Management Plans (RMP)

    • Renewals

    • Post-Approval Changes (PAC)

  • Drive lifecycle management strategies across product portfolios.

Health Authority Interactions

  • Lead interactions with global Health Authorities including:

    • FDA

    • EMA

    • PMDA

    • Other international regulatory agencies

  • Prepare briefing documents and meeting packages.

  • Coordinate agency meetings and regulatory discussions.

  • Lead meeting rehearsals and regulatory response strategies.

  • Document and communicate regulatory outcomes.

Core Labeling & Regulatory Strategy

  • Establish and maintain:

    • Company Core Data Sheet (CCDS)

    • Target CCDS

    • European Labeling

    • US Labeling Support Activities

  • Align Target Product Profiles (TPP) with commercial and market access objectives.

  • Drive labeling strategies throughout product lifecycle.

Regulatory Affairs Leadership

  • Serve as Subject Matter Expert across regulatory disciplines.

  • Develop regulatory best practices and process improvements.

  • Guide regulatory decision-making through risk-based assessments.

  • Mentor junior regulatory professionals and provide technical leadership.

Regulatory Due Diligence

  • Lead regulatory due diligence assessments.

  • Evaluate regulatory risks and opportunities.

  • Support business development and strategic decision-making.

  • Provide regulatory recommendations for portfolio investments and partnerships.

Clinical & Cross-Functional Support

  • Participate in or chair:

    • Clinical Project Teams

    • Cross-Functional Development Teams

    • Global Regulatory Working Groups

  • Provide regulatory input during product development and commercialization.

  • Collaborate with Medical Affairs, Clinical Operations, Safety, Quality, Legal, and Commercial teams.

Process Improvement & Compliance

  • Drive continuous improvement initiatives within Regulatory Affairs.

  • Identify opportunities to optimize submission processes and workflows.

  • Ensure compliance with global regulatory requirements and internal procedures.

  • Support inspection and audit readiness activities.

Educational Qualification

Required

  • Bachelor's Degree, Master's Degree, or PhD in:

    • Life Sciences

    • Pharmacy

    • Biotechnology

    • Biomedical Sciences

    • Medicine

    • Related Scientific Discipline

Experience Required

  • 7–9+ years of Regulatory Affairs experience.

  • Strong experience in:

    • Global Regulatory Affairs

    • Regulatory Strategy

    • Regulatory Submissions

    • Labeling

    • Health Authority Interactions

    • Lifecycle Management

  • Experience across major markets:

    • United States (FDA)

    • European Union (EMA)

    • China (NMPA)

    • Japan (PMDA)

  • Experience within pharmaceutical, biotechnology, or healthcare industries.