Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Associate Regulatory Specialist

Novo Nordisk
7-9 years
Not Disclosed
Bangalore, India
1 June 5, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill

Associate Regulatory Specialist – RA Diabetes

Department: Global Regulatory Affairs (RA Diabetes)
Function: Regulatory Affairs & Safety Pharmacovigilance
Location: Bangalore, Karnataka, India
Employment Type: Full-Time
Experience Required: 7–9+ Years
Industry: Pharmaceutical / Biotechnology / Life Sciences


Position Overview

We are seeking an experienced and strategic Associate Regulatory Specialist to join the Global Regulatory Affairs (RA Diabetes) team. In this role, you will drive global regulatory strategies and submissions supporting diabetes products throughout their development and lifecycle.

As a key regulatory professional, you will independently manage complex regulatory activities, engage directly with global health authorities, contribute to regulatory strategy development, and support cross-functional teams in delivering innovative therapies to patients worldwide.

The successful candidate will combine strong regulatory expertise, scientific knowledge, and stakeholder management capabilities to ensure successful regulatory approvals and lifecycle management across major international markets.


Key Responsibilities

Global Regulatory Submissions

  • Develop, execute, and maintain Regulatory Affairs Submission Plans within Vault RIM and other regulatory systems.

  • Prepare, compile, review, publish, and submit regulatory dossiers to global health authorities.

  • Manage submissions across multiple regulatory pathways including:

    • Marketing Authorization Applications (MAA)

    • New Drug Applications (NDA)

    • Biologics License Applications (BLA)

    • Clinical Trial Applications (CTA)

    • Investigational New Drug Applications (IND)

    • Pediatric Investigation Plans (PIP)

    • Pediatric Study Plans (PSP)

  • Coordinate renewals, variations, post-approval changes, and lifecycle management activities.

  • Prepare and submit pharmacovigilance and safety-related regulatory documents, including:

    • Development Safety Update Reports (DSUR)

    • Periodic Safety Update Reports (PSUR)

    • Risk Management Plans (RMP)


Health Authority Interactions

  • Lead and coordinate interactions with global regulatory agencies, including:

    • U.S. Food and Drug Administration (FDA)

    • European Medicines Agency (EMA)

    • Pharmaceuticals and Medical Devices Agency (PMDA)

    • National Medical Products Administration (NMPA)

    • Other international health authorities

  • Prepare meeting requests, briefing documents, and regulatory communication packages.

  • Lead internal preparation meetings and rehearsal sessions.

  • Document meeting outcomes and ensure timely follow-up on regulatory commitments.

  • Provide strategic regulatory guidance based on authority feedback and evolving requirements.


Regulatory Strategy & Labeling

  • Contribute to the development and execution of global regulatory strategies for diabetes products.

  • Establish and maintain:

    • Company Core Data Sheet (CCDS)

    • European Product Information

    • Core Labeling Documents

  • Align Target Product Profiles (TPPs) with regulatory, commercial, and market access objectives.

  • Support U.S. labeling development and global lifecycle management initiatives.

  • Assess regulatory risks and provide recommendations to optimize submission success.


Regulatory Process Excellence

  • Serve as a subject matter expert in one or more regulatory disciplines.

  • Identify opportunities for process improvements and operational efficiencies.

  • Drive implementation of best practices within regulatory operations and submissions management.

  • Contribute to the development of regulatory methodologies, tools, and standards.

  • Support digital transformation and continuous improvement initiatives.


Regulatory Due Diligence

  • Lead and contribute to regulatory due diligence activities for business development initiatives.

  • Assess regulatory risks, opportunities, and compliance considerations.

  • Provide strategic regulatory insights supporting portfolio and investment decisions.


Cross-Functional Collaboration

  • Participate in and lead cross-functional project teams and governance forums.

  • Collaborate closely with:

    • Clinical Operations

    • Medical & Scientific Affairs

    • Global Safety

    • Pharmacovigilance

    • Regulatory Operations

    • Clinical Pharmacology

    • Quality Assurance

    • Legal Affairs

    • Global Marketing

    • Market Access Teams

  • Provide regulatory expertise throughout product development and commercialization.


Mentorship & Leadership

  • Mentor junior regulatory professionals and support capability-building initiatives.

  • Share knowledge and best practices across the organization.

  • Contribute to training and development activities.

  • Promote a culture of collaboration, accountability, and continuous learning.


Required Qualifications

Education

One of the following qualifications is required:

  • PhD in Life Sciences, Pharmacy, Biotechnology, Pharmacology, Medicine, or related scientific discipline

OR

  • Master's Degree in a relevant life sciences field

OR

  • Bachelor's Degree in Life Sciences or equivalent scientific discipline with substantial regulatory experience

Equivalent practical experience may be considered.