Medtronic Regulatory Affairs Specialist Job in Gurgaon 2026
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(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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