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Regulatory Professional

Novo Nordisk
7+ years
22 LPA - 35 LPA
Bangalore, India
1 June 22, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Regulatory Affairs, Regulatory Writing, Regulatory Compliance, Global Submissions, eCTD, IND/NDA/BLA Submissions, ICH-GCP, Regulatory Strategy, Regulatory Intelligence, Labeling Strategy.

Regulatory Professional

Location: Bangalore, India
Company: Novo Nordisk Global Business Services (GBS)
Department: Regulatory Affairs & Safety Pharmacovigilance
Employment Type: Full-Time


Role Summary

The Regulatory Professional is responsible for driving global regulatory strategy, submission planning, and regulatory execution across multiple health authorities worldwide. The role supports the development, registration, lifecycle management, and commercialization of innovative pharmaceutical products by ensuring timely, compliant, and strategic regulatory submissions.

Working closely with global affiliates, health authorities, Regulatory Affairs teams, and cross-functional stakeholders, the Regulatory Professional contributes to regulatory intelligence, health authority interactions, lifecycle management activities, and continuous improvement initiatives across the product development lifecycle.


Key Responsibilities

Global Regulatory Strategy & Submissions

  • Develop and execute global regulatory submission strategies.

  • Lead planning, preparation, maintenance, and submission of regulatory dossiers.

  • Drive submission activities for:

    • MAA (Marketing Authorization Applications)

    • NDA (New Drug Applications)

    • BLA (Biologics License Applications)

    • CTA (Clinical Trial Applications)

    • IND (Investigational New Drug Applications)

    • Site Master Files

    • Renewals

    • Post-Approval Variations

    • Regulatory Commitments

  • Ensure timely submission and approval of regulatory deliverables.

Health Authority Interactions

  • Support preparation and execution of interactions with global regulatory authorities.

  • Participate in:

    • Regulatory Meetings

    • Meeting Requests

    • Briefing Packages

    • Rehearsals

    • Meeting Minutes Documentation

  • Collaborate with affiliates in preparation for local regulatory authority engagements.

Regulatory Lifecycle Management

  • Manage product lifecycle regulatory activities.

  • Support:

    • Renewals

    • Label Updates

    • Post-Approval Changes

    • Regulatory Commitments

  • Monitor regulatory timelines and ensure compliance with submission schedules.

  • Conduct strategic planning for global renewals and lifecycle activities.

Regulatory Intelligence & Compliance

  • Monitor and interpret emerging regulatory requirements and guidelines.

  • Assess impact of evolving regulations across global markets.

  • Provide regulatory intelligence and strategic recommendations.

  • Ensure regulatory compliance throughout the product lifecycle.

Cross-Functional Collaboration

  • Represent Regulatory Affairs within global matrix teams.

  • Collaborate with:

    • Clinical Development

    • Medical Affairs

    • Pharmacovigilance

    • Quality Assurance

    • CMC Teams

    • Project Management Teams

    • Global Affiliates

  • Ensure alignment of regulatory strategy with development and commercialization plans.

Regulatory Systems & Documentation

  • Manage submission planning and tracking using regulatory systems such as Vault RIM.

  • Review and maintain regulatory documentation.

  • Assess country-specific documentation requirements.

  • Ensure regulatory records remain accurate, complete, and inspection-ready.

Innovation & Continuous Improvement

  • Contribute to innovation initiatives within Regulatory Affairs.

  • Support process optimization and operational excellence programs.

  • Drive improvements in submission planning, execution, and regulatory workflows.

  • Promote adoption of regulatory best practices and digital solutions.

Mentoring & Capability Development

  • Mentor and train junior regulatory professionals.

  • Share regulatory expertise and best practices.

  • Support capability-building initiatives within the Regulatory Affairs function.

  • Contribute to team development and knowledge sharing.


Required Qualifications

Education

  • Master’s Degree in:

    • Pharmacy

    • Life Sciences

    • Biotechnology

    • Regulatory Affairs

    • Related Scientific Discipline


Experience

  • Minimum 7+ years of Regulatory Affairs experience.

  • Experience supporting global regulatory submissions and lifecycle management.

  • Exposure to regulatory requirements across:

    • EU

    • US

    • China

    • Japan

  • Experience within pharmaceutical, biotechnology, or life sciences organizations.