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Regulatory Professional

Novo Nordisk
7+ years
INR 28 LPA – 35 LPA
Bangalore, India
1 June 19, 2026
Job Description
Job Type: Hybrid 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

Department: Regulatory Affairs & Safety Pharmacovigilance
Location: Bangalore, Karnataka, India
Employment Type: Full-Time
Work Mode: Hybrid / On-Site

Role Summary

The Regulatory Professional is responsible for driving global regulatory strategy, regulatory submissions, and health authority interactions across multiple markets. This role plays a key part in ensuring successful development, registration, approval, and lifecycle management of pharmaceutical products by collaborating with global stakeholders, affiliates, and regulatory authorities.

The position requires deep expertise in regulatory affairs, strategic planning, regulatory intelligence, and global submission management, with a strong focus on delivering innovative therapies to patients while ensuring compliance with evolving global regulations.

Key Responsibilities

Global Regulatory Strategy & Submission Management

  • Lead regulatory submission planning and execution across global health authorities.

  • Develop and implement regulatory strategies supporting:

    • Product Development

    • Product Registration

    • Lifecycle Management

    • Market Expansion Initiatives

  • Drive preparation, maintenance, and submission of regulatory dossiers, including:

    • Marketing Authorization Applications (MAA)

    • New Drug Applications (NDA)

    • Biologics License Applications (BLA)

    • Clinical Trial Applications (CTA)

    • Investigational New Drug Applications (IND)

    • Site Master Files

    • Product Renewals

    • Post-Approval Changes

    • Regulatory Commitments

  • Ensure submission quality, compliance, and adherence to regulatory timelines.

Health Authority Engagement & Regulatory Communication

  • Support planning and execution of interactions with global health authorities.

  • Contribute to:

    • Meeting Requests

    • Briefing Packages

    • Regulatory Meeting Preparation

    • Rehearsals and Mock Sessions

    • Meeting Minutes and Documentation

  • Provide regulatory guidance to affiliates preparing for authority interactions.

  • Support responses to regulatory questions, requests, and commitments.

  • Facilitate effective communication between internal teams and regulatory agencies.

Regulatory Representation & Cross-Functional Collaboration

  • Represent Regulatory Affairs within global matrix teams.

  • Ensure alignment of regulatory strategy and development plans across functions.

  • Maintain effective communication between:

    • Regulatory Affairs

    • Clinical Development

    • CMC

    • Quality

    • Pharmacovigilance

    • Project Management

    • Commercial Teams

  • Contribute to strategic decision-making throughout the product lifecycle.

Regulatory Operations & Lifecycle Management

  • Monitor and manage upcoming regulatory submissions using:

    • Vault RIM

    • Regulatory Tracking Systems

    • Submission Planning Tools

  • Assess country-specific and regional documentation requirements.

  • Drive planning and execution of:

    • Global Renewals

    • Variations

    • Label Updates

    • Post-Approval Commitments

  • Ensure compliance with global regulatory timelines and obligations.

Regulatory Intelligence & Innovation

  • Monitor evolving global regulatory requirements and industry trends.

  • Analyze emerging guidelines from:

    • FDA

    • EMA

    • PMDA

    • NMPA

    • Other Global Regulatory Authorities

  • Provide regulatory intelligence to support strategic decision-making.

  • Participate in innovation initiatives aimed at enhancing regulatory processes, tools, and efficiencies.

  • Support continuous improvement within the Regulatory Affairs function.

Mentorship & Capability Development

  • Mentor and support junior regulatory professionals.

  • Share regulatory expertise and best practices across teams.

  • Contribute to training programs and capability-building initiatives.

  • Foster a culture of continuous learning and knowledge sharing.

Required Qualifications

Education

  • Master's Degree in:

    • Pharmacy

    • Life Sciences

    • Biotechnology

    • Pharmaceutical Sciences

    • Regulatory Science

    • Related Scientific Discipline

Experience

  • Minimum 7+ years of relevant experience in Regulatory Affairs within:

    • Pharmaceutical Industry

    • Biotechnology Industry

    • Healthcare Sector

  • Proven experience managing global regulatory submissions and health authority interactions.

  • Experience across:

    • Early-Stage Development

    • Late-Stage Development

    • Product Registration

    • Lifecycle Management

    • Label Development