Is this a hybrid work opportunity?

Yes, this role follows a hybrid work model in Gurugram.

What is the expected salary for this role?

The estimated salary range is approximately ₹10 LPA to ₹22 LPA depending on experience.

Is this Advarra job suitable for freshers?

Yes, this role is suitable for freshers and candidates with up to 1 year of experience.

What systems are used in this role?

Candidates will work on CTMS, EDC platforms, CRF development, and clinical research workflows.

What is the salary for Research Associate I at Advarra?

The estimated salary ranges from ₹3.2 LPA to ₹5.5 LPA depending on skills and experience.

What qualifications are required for this role?

Candidates should have a degree in Pharmacy, Life Sciences, Biotechnology, Nursing, or related fields.

Medtronic Regulatory Affairs Specialist Job in Gurgaon 2026

Q: What is the job role offered by Medtronic India?

Medtronic India is hiring for the position of Regulatory Affairs Specialist.

Q: What experience is required for this position?

Candidates should have 5–10 years of experience including medical device regulatory affairs exposure.

(Medtronic Regulatory Affairs Specialist Job in Gurgaon 2026)

Introduction

Medtronic India has announced a new hiring opportunity for experienced Regulatory Affairs professionals in Gurugram, Haryana. The company is actively recruiting skilled candidates for the position of Regulatory Affairs Specialist in its Medical Devices and Equipment division. This hybrid opportunity is ideal for professionals with expertise in CDSCO submissions, medical device registrations, clinical trial approvals, import licenses, and regulatory compliance activities.

Candidates from B Pharma, M Pharma, Biomedical Engineering, and Life Sciences backgrounds looking for high-paying Regulatory Affairs jobs in India can explore this excellent career opportunity with one of the world’s leading healthcare technology companies. The role provides exposure to global regulatory systems, international compliance projects, and advanced medical device approvals.

About Medtronic

Medtronic is a globally recognized medical technology company headquartered in Dublin, Ireland. Founded in 1949, the organization operates in more than 150 countries and develops innovative medical devices, healthcare technologies, and therapy solutions for patients worldwide. The company employs more than 95,000 professionals globally and focuses on improving healthcare outcomes through innovation and advanced medical technologies.

Medtronic India plays an important role in regulatory affairs, medical device approvals, compliance management, and healthcare technology operations across the Indian subcontinent. The organization works closely with global healthcare authorities and regulatory agencies to ensure patient safety and product compliance.

Company Details

Particulars	Information
Company Name	Medtronic
Headquarters	Dublin, Ireland
Founded	1949
Industry	Medical Devices & Healthcare Technology
Global Presence	150+ Countries
Employees	95,000+ Employees Worldwide
Work Model	Hybrid
Job Location	Gurugram, Haryana

Job Overview Summary

Medtronic is hiring experienced Regulatory Affairs professionals to manage medical device registrations, regulatory submissions, import licensing, compliance documentation, and post-approval regulatory activities. The selected candidate will coordinate with CDSCO, FDA, DGDA, AERB, and global regulatory teams while ensuring compliance with Indian and international medical device regulations.

This role is highly suitable for professionals experienced in Regulatory Affairs, Medical Device Compliance, Clinical Trial Regulatory Approvals, and Quality Systems Management.

Vacancy Details

Job Details	Information
Job Title	Regulatory Affairs Specialist
Company	Medtronic
Location	Gurugram
Work Mode	Hybrid
Employment Type	Full-Time
Industry	Medical Devices & Equipment
Qualification	B Pharma, M Pharma, Biomedical Engineering, Life Sciences
Experience Required	5–10 Years
Department	Regulatory Affairs
Application Mode	Online

Job Role Explanation

The Regulatory Affairs Specialist will manage end-to-end regulatory processes for medical devices and healthcare products across India and neighboring countries. The role involves preparing regulatory dossiers, coordinating approvals, maintaining compliance documentation, and ensuring adherence to global regulatory standards.

Selected candidates will work closely with internal business teams, international regulatory departments, clinical teams, and government agencies to ensure timely product registrations and approvals.

Major Responsibilities

Preparation and submission of regulatory dossiers
Managing product registration and renewal applications
Handling import licenses and regulatory approvals
Monitoring CDSCO and global regulatory updates
Supporting clinical trial approvals for medical devices
Coordinating with the FDA, DGDA, State FDA, and AERB authorities
Managing post-approval compliance activities
Supporting adverse event reporting and field actions
Maintaining SOPs, regulatory trackers, and archival systems
Collaborating with cross-functional international teams

Eligibility Criteria

Candidates applying for this Medtronic Regulatory Affairs Specialist role should meet the following qualifications:

Educational Qualification

Applicants must possess any of the following qualifications:

B Pharma
M Pharma
Biomedical Engineering Degree
Life Sciences Degree
Related Science or Healthcare Qualification

Experience Required

5–10 years of total experience
Minimum 2–3 years in Medical Device Regulatory Affairs
Experience in regulatory submissions and approvals preferred

Skills Required

Medtronic is looking for professionals with strong regulatory and compliance expertise in the healthcare and medical device sector.

Required Skills

Knowledge of CDSCO regulations
Medical device registration expertise
Regulatory dossier preparation
Clinical trial approval management
Import license handling
FDA and CE regulatory understanding
Quality systems and compliance knowledge
Strong documentation management
Excellent coordination and communication abilities
Problem-solving and analytical skills

Preferred Technical Knowledge

Regulatory tracking systems
SOP management
Post-market surveillance
Adverse event reporting
Compliance audits
Change control management

Salary Estimate

Based on current market trends for Regulatory Affairs Specialist jobs in Gurgaon and Bengaluru healthcare sectors, the estimated salary range for this role is:

Expected Salary Range

₹10 LPA – ₹22 LPA (Approximate)

Actual salary may vary depending on:

Regulatory Affairs experience
Medical device industry expertise
Global compliance exposure
Technical and communication skills
Previous compensation package

Why Join Medtronic?

Working with Medtronic offers candidates an opportunity to build long-term careers in global healthcare technology and medical device compliance.

Employee Benefits

Hybrid work flexibility
International regulatory exposure
Career growth in Medical Device Regulatory Affairs
Advanced healthcare technology projects
Learning and development programs
Opportunity to work with global teams
Exposure to clinical trial regulatory approvals
Stable and innovation-focused work environment

Interview Details

Currently, Medtronic has not officially announced interview dates for this position. Shortlisted candidates may be contacted by the HR or Talent Acquisition team for further selection rounds.

Expected Selection Process

Resume Shortlisting
HR Discussion
Technical Interview
Regulatory Affairs Assessment
Final Managerial Round

Required Documents

Candidates applying for this Medtronic Regulatory Affairs job should keep the following documents ready:

Updated Resume/CV
Educational Certificates
Experience Certificates
Government ID Proof
Latest Salary Slip
Passport Size Photograph
Regulatory Affairs Training Certificates (if available)
Clinical Trial or Compliance Certifications

Job Location

Work Location

Gurugram, Haryana, India

Work Mode

Hybrid Work Opportunity

Candidates may be required to attend office operations, along with remote work flexibility, depending on project requirements.

How to Apply

Interested and eligible candidates can apply online using the official application link below:

Application Link:

Candidates are advised to apply as early as possible because hiring may close once positions are filled.

Frequently Asked Questions (FAQs)

Q1. What is the job role offered by Medtronic India?

Medtronic is hiring for the position of Regulatory Affairs Specialist.

Q2. What qualifications are required for this Medtronic job?

Candidates with B Pharma, M Pharma, Biomedical Engineering, and Life Sciences qualifications can apply.

Q3. Is this a work-from-home job?

No. This is a Hybrid work opportunity based in Gurugram.

Q4. What experience is required for this position?

Candidates should have approximately 5–10 years of experience, including medical device regulatory affairs exposure.

Q5. What is the expected salary for this Regulatory Affairs Specialist role?

The estimated salary range is approximately ₹10 LPA – ₹22 LPA, depending on experience and expertise.

Q6. Which regulatory authorities will candidates work with?

Selected candidates may coordinate with CDSCO, FDA, DGDA, State FDA, and AERB.

Q7. Is knowledge of CDSCO regulations mandatory?

Yes, understanding CDSCO and medical device regulatory processes is highly preferred.

Q8. Can Pharmacy graduates apply for this role?

Yes. B Pharma and M Pharma candidates with relevant experience are eligible.

Final Conclusion

The Medtronic Regulatory Affairs Specialist job in Gurgaon offers an outstanding opportunity for experienced professionals looking to advance their careers in medical device regulatory affairs and healthcare compliance. Candidates with strong expertise in CDSCO regulations, medical device registrations, clinical trial approvals, and compliance management can gain valuable global exposure while working with one of the world’s leading healthcare technology companies.

This opportunity is especially beneficial for professionals aiming to build long-term careers in Regulatory Affairs, Medical Devices, Clinical Compliance, and International Healthcare Operations.

Candidates are advised to review the eligibility criteria carefully and apply online at the earliest.

Disclaimer

Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.

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