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Regulatory Professional Ii

Novo Nordisk
6+ years
INR 15 LPA – 25 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 Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs

Regulatory Professional II

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

Position Summary

The Regulatory Professional II is responsible for supporting global regulatory submissions, regulatory strategy execution, lifecycle management activities, and maintenance of marketing authorizations across regulated and emerging markets. The role focuses on Regulatory Affairs CMC (RA-CMC), submission planning, health authority interactions, regulatory intelligence, and stakeholder management to ensure timely approvals and compliance throughout the product lifecycle.

Key Responsibilities

Regulatory Submission Management

  • Support planning, preparation, review, and submission of regulatory dossiers globally.

  • Develop and maintain Regulatory Submission Plans.

  • Coordinate submission activities across multiple markets and regions.

  • Ensure timely delivery of regulatory filings according to business timelines.

  • Support NDA submissions and global product registrations.

Regulatory Strategy & Intelligence

  • Apply regulatory intelligence to support submission planning and regulatory decision-making.

  • Contribute to development of regulatory strategies for product registrations and lifecycle activities.

  • Monitor evolving regulatory requirements and assess business impact.

  • Support implementation of regulatory strategies across global markets.

RA-CMC & Regulatory Documentation

  • Establish and maintain the CMC section of core regulatory files.

  • Review and support preparation of regulatory documents and technical dossiers.

  • Ensure regulatory documentation meets Health Authority requirements.

  • Support regulatory compliance throughout product lifecycle.

Life Cycle Management (LCM)

  • Manage post-approval lifecycle activities.

  • Support:

    • Renewals

    • Variations

    • Change Requests (CR)

    • Deviations

    • Annual Reports

    • Post Approval Changes (PACs)

  • Maintain global marketing authorizations.

  • Ensure timely implementation of regulatory changes.

Health Authority Interactions

  • Support responses to Regulatory Submission Inquiries (RSI).

  • Prepare responses to Health Authority (HA) questions and deficiency letters.

  • Coordinate regulatory communication with global agencies.

  • Support regulatory inspections and compliance activities when required.

Regulatory Systems & Compliance

  • Utilize Veeva Vault Submissions and Registrations platforms.

  • Maintain accurate regulatory records and submission tracking.

  • Ensure compliance with regulatory processes, SOPs, and global standards.

  • Support document management and regulatory operations activities.

Stakeholder Management

  • Collaborate with:

    • Regulatory Affairs Teams

    • CMC Teams

    • Manufacturing

    • Quality Assurance

    • Clinical Development

    • Global Affiliates

  • Build strong relationships across countries, functions, and cultures.

  • Facilitate efficient communication among stakeholders.

Project Management

  • Manage multiple regulatory projects simultaneously.

  • Track submission milestones and deliverables.

  • Support global launch activities and market expansion projects.

  • Drive regulatory activities to minimize time-to-market.

Educational Qualification

Required

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

    • Pharmacy

    • Life Sciences

    • Biotechnology

    • Chemistry

    • Medicine

    • Biotechnology Engineering

    • Related Scientific Discipline

Experience Required

  • Minimum 6+ years of Regulatory Affairs experience.

  • Strong experience in:

    • Regulatory Submissions

    • Regulatory Affairs CMC (RA-CMC)

    • Regulatory Operations

    • Lifecycle Management

    • Global Regulatory Affairs

  • Experience supporting both regulated and emerging markets.

  • Exposure to China and Japan regulatory markets preferred.

  • Experience working in global and affiliate regulatory environments.