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Regulatory Affairs Specialist

Medtronic
5-7 years
INR 12 LPA – 22 LPA
Gurgaon, India
1 June 24, 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 AFFAIRS SPECIALIST

Company: Medtronic
Location: Gurgaon, Haryana, India
Department: Regulatory Affairs – India Subcontinent
Job Type: Full-Time


JOB OVERVIEW

The Regulatory Affairs Specialist is responsible for managing regulatory registrations, import licenses, clinical trial approvals, product renewals, post-approval changes, and regulatory compliance activities for Medtronic products across the Indian Subcontinent (India, Sri Lanka, Bangladesh, and Nepal).

This role serves as the key interface between Medtronic business units, global regulatory teams, regulatory authorities, and healthcare agencies to ensure uninterrupted business operations through timely regulatory approvals and compliance management.


KEY RESPONSIBILITIES

Regulatory Submission & Registration Management

  • Prepare, review, and submit regulatory dossiers for:

    • Product registrations

    • Re-registrations

    • Import licenses

    • Product renewals

    • Product amendments

  • Track submission progress with regulatory authorities.

  • Ensure timely approvals to support product launches and business continuity.

Regulatory Strategy & Compliance

  • Support development and execution of regulatory strategies for:

    • New products

    • Product modifications

    • Clinical trials

    • Line extensions

  • Ensure compliance with local and international regulatory requirements.

  • Interpret and implement regulatory laws and guidelines.

Post-Approval Change Management

  • Review product change controls.

  • Assess regulatory impact of:

    • Manufacturing changes

    • Labeling changes

    • Design modifications

    • Product updates

  • Coordinate post-approval submissions and variations.

Clinical Trial Regulatory Support

  • Collaborate with Clinical Affairs teams on:

    • Clinical Trial Applications (CTA)

    • Test Licenses

    • Import Licenses for clinical trials

    • Protocol amendments

  • Support approvals from regional regulatory authorities.

Regulatory Agency Liaison

  • Serve as a primary contact for:

    • CDSCO

    • State FDA Authorities

    • CDDA (Sri Lanka)

    • DGDA (Bangladesh)

    • DoT

    • AERB

  • Coordinate submissions, approvals, amendments, and compliance matters.

Quality & Regulatory Compliance

  • Ensure continuous compliance with:

    • CDSCO Medical Device Rules

    • FDA Requirements

    • CE Regulations

    • Quality Management Systems

  • Support adverse event and field action reporting.

  • Maintain inspection readiness.

Regulatory Intelligence

  • Monitor changes in:

    • Indian regulations

    • Global medical device regulations

  • Assess business impact and communicate updates to stakeholders.

  • Recommend compliance actions.

Regulatory Systems & Documentation

  • Maintain:

    • SOPs

    • Regulatory trackers

    • Archival systems

    • Regulatory databases

  • Ensure document control and traceability.

Tender & Business Support

  • Provide regulatory support for:

    • Government tenders

    • Product commercialization activities

    • Market access initiatives


REQUIRED SKILLS

Regulatory Affairs Skills

  • Medical Device Registration

  • Import License Management

  • Regulatory Dossier Preparation

  • Post-Approval Change Management

  • Clinical Trial Regulatory Submissions

  • Regulatory Compliance

  • Regulatory Strategy Development

  • Regulatory Intelligence

Regulatory Knowledge

  • CDSCO Medical Device Rules

  • Medical Device Registration Requirements

  • Clinical Trial Regulations

  • FDA Regulations

  • CE Regulations

  • Quality Management Systems

  • Design Control Requirements

  • Product Lifecycle Management

Technical Skills

  • Regulatory Documentation Systems

  • Microsoft Office Suite

  • Regulatory Tracking Tools

  • Document Management Systems

Soft Skills

  • Regulatory Writing

  • Stakeholder Management

  • Communication Skills

  • Government Agency Interaction

  • Negotiation Skills

  • Planning & Organization

  • Problem Solving

  • Time Management


EDUCATIONAL QUALIFICATIONS

Required

  • B.Pharm / M.Pharm

OR

  • Bachelor's / Master's Degree in:

    • Biomedical Engineering

    • Life Sciences

    • Biotechnology

    • Healthcare-related disciplines

Preferred

  • Regulatory Affairs Training or Certification

  • RAC (Regulatory Affairs Certification)


EXPERIENCE REQUIREMENTS

Required

  • 5–7 years total experience in:

    • Pharma

    • Medical Devices

    • Life Sciences

Mandatory

  • Minimum 2–3 years Medical Device Regulatory Affairs experience.