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

Regulatory Affairs Specialist

Medtronic
5-7 years
Not Disclosed
Gurgaon, India
1 June 5, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development

Regulatory Affairs Specialist – Medtronic

Company: Medtronic
Job ID: R66375
Location: Gurgaon, Haryana, India
Work Arrangement: Flexible Work Arrangement
Experience: 5–7 Years
Industry: Medical Devices / Regulatory Affairs
Career Level: Specialist (Individual Contributor)


Role Overview

The Regulatory Affairs Specialist is responsible for managing regulatory submissions, registrations, renewals, import licenses, clinical trial approvals, and post-market regulatory compliance for Medtronic's medical device portfolio across the Indian Subcontinent.

The role serves as a critical link between business units, global regulatory teams, supply chain, quality, clinical affairs, and regulatory authorities to ensure uninterrupted market access and regulatory compliance.

This is a highly specialized Medical Device Regulatory Affairs position focused on India, Sri Lanka, Bangladesh, and Nepal.


Key Responsibilities

Regulatory Submissions & Registrations

  • Prepare, review, and submit regulatory dossiers.

  • Manage:

    • Product registrations

    • Registration renewals

    • Import licenses

    • Amendments and variations

    • Labeling approvals

    • Line extensions

  • Track applications through approval lifecycle.

Regulatory Strategy & Coordination

  • Collaborate with global regulatory teams.

  • Support local business units with regulatory requirements.

  • Provide strategic guidance for market authorization activities.

  • Ensure alignment between global and local regulatory expectations.

Regulatory Compliance Management

  • Maintain compliance with country-specific medical device regulations.

  • Monitor changes in regulatory requirements.

  • Assess regulatory impact on products and business operations.

  • Ensure timely reporting of:

    • Adverse events

    • Field Safety Corrective Actions

    • Product changes

    • Post-market obligations

Change Control Management

  • Evaluate product changes received from manufacturing and global teams.

  • Determine regulatory filing requirements.

  • Manage post-approval change submissions.

  • Ensure ongoing regulatory compliance throughout product lifecycle.

Clinical Trial Regulatory Support

Work with Clinical Affairs teams to obtain:

  • Clinical Trial Approvals

  • Test Licenses

  • Import Licenses for Clinical Studies

  • Amendment Approvals

  • Ethics and regulatory documentation support

Government & Authority Interaction

Coordinate with regulatory authorities including:

  • Central Drugs Standard Control Organization

  • State Food and Drug Administration

  • Atomic Energy Regulatory Board

Responsibilities include:

  • Submission follow-up

  • Regulatory meetings

  • Compliance discussions

  • Approval tracking

Regulatory Systems & Documentation

  • Maintain regulatory SOPs.

  • Manage regulatory archives.

  • Maintain regulatory trackers.

  • Support document management systems.

  • Ensure quality and audit readiness.

Business Support

  • Support Marketing teams on tender-related regulatory requirements.

  • Assist Supply Chain teams in maintaining uninterrupted product availability.

  • Support business continuity through proactive regulatory planning.


Educational Requirements

Preferred Qualifications

  • B.Pharm

  • M.Pharm

  • Bachelor's Degree in Biomedical Engineering

  • Master's Degree in Biomedical Engineering

  • Life Sciences Degree

  • Formal Regulatory Affairs Training


Experience Requirements

Mandatory

  • 5–7 years of experience in:

    • Medical Devices

    • Pharmaceuticals

    • Life Sciences

Essential

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