Medtronic is hiring for the position of Senior Regulatory Affairs Specialist in Nanakramguda, Hyderabad. This is a full-time opportunity with a flexible work arrangement for experienced regulatory affairs professionals from the medical device and/or pharmaceutical industry.
The selected candidate will support regulatory activities related to product development, international registrations, regulatory submissions, change controls, product modifications, audits and inspections. The role also involves developing regulatory strategies, maintaining regulatory information and coordinating with internal teams and regulatory authorities.
Medtronic Senior Regulatory Affairs Specialist Recruitment 2026 – Job Highlights
| Particular | Details |
|---|---|
| Company | Medtronic |
| Job Title | Senior Regulatory Affairs Specialist |
| Location | Nanakramguda, Hyderabad, India |
| Job Type | Full Time |
| Work Arrangement | Flexible Work Arrangement |
| Experience | 7+ Years |
| Qualification | Bachelor’s Degree in Relevant Field |
| Industry | Medical Devices / Pharmaceutical |
| Key Area | Regulatory Affairs |
| Requisition ID | R72459 |
| Salary | Competitive; Exact Amount Not Specified |
| Incentive | Eligible for Medtronic Incentive Plan (MIP) |
About Medtronic
Medtronic is a global healthcare technology company that develops and supports medical technologies across a wide range of healthcare areas. The company operates internationally and focuses on technologies intended to improve patient care.
The Senior Regulatory Affairs Specialist will contribute to regulatory activities supporting product development, registrations and ongoing compliance across international markets.
Job Description
The Senior Regulatory Affairs Specialist will support regulatory requirements associated with design and development controls, product registrations, regulatory submissions and changes to medical devices.
The position requires collaboration with business units, international regulatory affairs teams and other organizational departments. The role also involves preparing submission documentation, maintaining regulatory records, assessing regulatory impacts of changes and supporting communication with regulatory agencies or notified bodies.
Key Responsibilities
Regulatory Information Management
- Support the establishment and maintenance of processes for entering regulatory data into the Regulatory Information Management System.
- Serve as a subject matter expert for regulatory data processes.
- Provide guidance on the consistent interpretation of required regulatory data attributes.
- Maintain regulatory files, records, data and reporting systems.
- Improve tracking and information-retrieval processes for regulatory activities.
- Monitor regulatory information and changes that may affect assigned projects.
Regulatory Submissions and Registrations
- Prepare, review and maintain regulatory documentation for international product registrations.
- Support premarket documentation for assigned projects.
- Compile submission packages for global regulatory filings.
- Prepare documentation required for license renewals and annual registrations.
- Support internal audits and regulatory inspections.
- Coordinate regulatory documentation received from different company functions.
- Collaborate with business units and international regulatory affairs teams to support marketing authorizations.
Regulatory Strategy
- Develop regulatory strategies for new or modified products within assigned projects.
- Evaluate the regulatory impact of proposed product or process changes.
- Provide regulatory guidance to project teams.
- Recommend changes to labeling, manufacturing, marketing activities or clinical protocols where required for regulatory compliance.
- Prepare internal regulatory documents associated with device modifications.
Change Control and Compliance
- Review change-control documentation and determine potential regulatory impact.
- Conduct formal regulatory assessments for internal and external documents.
- Author or review regulatory procedures and update them when necessary.
- Monitor regulatory tracking and control systems.
- Recommend process or system improvements to increase effectiveness.
- Track changes in the regulatory environment and communicate their potential impact.
Regulatory Agency Communication
- Communicate with regulatory agencies and/or notified bodies on defined administrative and routine matters.
- Support regulatory communications related to assigned projects.
- Consolidate and maintain written and oral communication with health authorities.
- Provide regulatory information and documentation when required for business activities such as tenders.
Cross-Functional Collaboration
The role requires regular interaction with internal stakeholders across different functions.
Key activities include:
- Working with business units and international regulatory affairs teams.
- Sharing regulatory status, requirements and project information.
- Providing input for decision-making and project activities.
- Supporting project milestones.
- Building effective working relationships with internal stakeholders.
- Establishing credibility across different levels of the organization.
Educational Qualification / Eligibility Criteria
Candidates should have a Bachelor’s degree in a relevant discipline.
The vacancy mentions fields including:
- Medical Sciences
- Mechanical Engineering
- Electrical Engineering
- Life Sciences
- Other healthcare-related disciplines
The educational background should be relevant to regulatory affairs and the medical device or pharmaceutical industry.
Experience Requirements
Medtronic specifies:
- 7+ years of Regulatory Affairs experience in the medical device and/or pharmaceutical industry.
- Ability to work independently with general supervision.
- Experience handling moderately complex projects or assignments.
- Ability to contribute to project milestones.
- Experience improving systems and processes to solve problems or increase effectiveness.
The position is intended for an experienced regulatory affairs professional who can handle assigned responsibilities with a significant level of independence.
Required Skills
Candidates should demonstrate:
- Regulatory affairs knowledge
- International regulatory submission experience
- Regulatory documentation management
- Regulatory strategy development
- Regulatory impact assessment
- Change-control review
- Regulatory information management
- Strong written communication
- Strong verbal communication
- Organizational skills
- Interpersonal skills
- Problem-solving ability
- Project coordination
- Stakeholder management
- Ability to work independently
- Ability to work in a team environment
Preferred Skills
Medtronic also highlights the following desirable qualities:
- Excellent communication and interpersonal skills
- Strong organizational capabilities
- Flexible and team-oriented approach
- Self-motivation
- Positive working attitude
- Ability to quickly establish credibility with stakeholders
- Ability to communicate effectively with different levels of the organization
Work Location and Work Arrangement
Location: Nanakramguda, Hyderabad, India
Job Type: Full Time
Work Arrangement: Flexible Work Arrangement
The exact flexibility and working conditions will be subject to Medtronic’s applicable policies and business requirements.
Salary and Benefits
Medtronic states that it provides a competitive salary and flexible benefits package. However, the exact salary for this position has not been disclosed in the provided vacancy.
The position is also eligible for the Medtronic Incentive Plan (MIP), described as a short-term incentive.
Specific compensation and benefits may depend on applicable employment terms.
Selection Process
The detailed selection process has not been provided in the vacancy. Candidates should follow Medtronic’s official recruitment procedure and complete any interviews, assessments or other stages communicated by the company.
How to Apply for Medtronic Senior Regulatory Affairs Specialist Recruitment 2026
Interested and eligible candidates can apply online through the official Medtronic careers portal.
- Open the official Medtronic job listing.
- Review the qualification and experience requirements.
- Prepare an updated CV/resume highlighting relevant regulatory affairs experience.
- Submit the application through the official careers portal.
- Complete any additional recruitment steps requested by Medtronic.
Important Details Before Applying
- The position is located in Nanakramguda, Hyderabad.
- This is a full-time position.
- A flexible work arrangement is specified.
- Candidates should have 7+ years of Regulatory Affairs experience in the medical device and/or pharmaceutical industry.
- A Bachelor’s degree in a relevant medical, engineering, life sciences or healthcare-related field is specified.
- Experience with international regulatory submissions is relevant.
- Knowledge of regulatory information management and regulatory documentation is important.
- The role involves change-control and regulatory impact assessments.
- The position may involve communication with regulatory agencies and notified bodies.
- Medtronic states that the position is eligible for the Medtronic Incentive Plan (MIP).
- Exact salary has not been disclosed.
Medtronic Recruitment Fraud Alert
Medtronic advises job seekers to apply only through its official recruitment channels. Legitimate Medtronic recruiting communications use approved Medtronic platforms and official @medtronic.com email addresses.
Candidates should be cautious of requests for payment or sensitive financial information during recruitment. Medtronic states that it will not request payment or sensitive information such as bank account details during the early stages of the hiring process.
If you receive a suspicious communication claiming to represent Medtronic, do not respond, click unknown links or open unexpected attachments.
For concerns about the authenticity of a Medtronic recruitment communication, the vacancy provides AskHR@medtronic.com as the contact address.
Frequently Asked Questions
1. What position is Medtronic hiring for?
Medtronic is hiring for the position of Senior Regulatory Affairs Specialist.
2. Where is the job located?
The position is based in Nanakramguda, Hyderabad, India.
3. How much experience is required?
The vacancy requires 7+ years of Regulatory Affairs experience in the medical device and/or pharmaceutical industry.
4. What educational qualification is required?
A Bachelor’s degree in a relevant medical, mechanical, electrical, life sciences or healthcare-related discipline is specified.
5. What are the main responsibilities?
The role includes regulatory submissions, international registrations, regulatory strategy, regulatory information management, change-control assessments, regulatory documentation and communication with regulatory authorities.
6. Does the role involve international regulatory submissions?
Yes. The position includes preparing documentation packages for international regulatory submissions and supporting global registrations.
7. Does the position involve regulatory agencies?
Yes. The role may involve communication with regulatory agencies and notified bodies on defined matters.
8. Does the role involve change control?
Yes. The position includes reviewing change-control documents and assessing their regulatory impact.
9. Is the position full time?
Yes. It is listed as a full-time position.
10. What is the work arrangement?
The vacancy specifies a Flexible Work Arrangement.
11. What is the salary?
The exact salary has not been disclosed. Medtronic describes the compensation as competitive and states that the position is eligible for the Medtronic Incentive Plan.
12. What is the job requisition number?
The requisition ID is R72459.
Important Note
Job availability, eligibility criteria, compensation, work arrangements and recruitment conditions may change. Candidates should verify the latest information on the official Medtronic careers portal before applying.