Medtronic is hiring a Regulatory Affairs Specialist for its Nanakramguda, Hyderabad location. The position is a full-time opportunity with a Flexible Work Arrangement and is suitable for professionals with 4–7 years of regulatory affairs experience in the medical device and/or pharmaceutical industry.
The role focuses on regulatory strategy, global product registrations, premarket submissions, regulatory assessments, health-authority communication, labeling and promotional-material review, and regulatory support for product development and modifications.
Job Details
| Particular | Details |
|---|---|
| Company | Medtronic |
| Position | Regulatory Affairs Specialist |
| Job ID | R73651 |
| Location | Nanakramguda, Hyderabad, Telangana |
| Employment Type | Full Time |
| Work Arrangement | Flexible Work Arrangement |
| Experience | 4–7 Years |
| Industry | Medical Devices / Healthcare / Pharmaceutical |
| Qualification | Bachelor’s degree in Medical, Mechanical, Electrical, Life Science or related healthcare discipline |
| Posted | September 18, 2026 |
Author: Pharmabharat Editorial Team
About Medtronic
Medtronic is a global healthcare technology company whose stated mission is to alleviate pain, restore health and extend life. Its careers organization includes opportunities across regulatory, quality, clinical, engineering, research and development and other functions.
In India, Medtronic’s Engineering & Innovation Center is located in Hyderabad. The company says the center contributes to new product development, released product management, customer quality and regulatory functions and works with Medtronic business units globally.
Medtronic Regulatory Affairs Specialist Job Description
As a Regulatory Affairs Specialist, the selected professional will support design and development control activities by providing regulatory requirements, direction, tactics and strategies. The position involves collaboration with business-unit teams, international regulatory professionals and other organizational functions.
The role has a strong focus on medical device regulatory affairs, global registrations, regulatory submissions and maintaining compliance throughout product development and modification activities.
Key Responsibilities
The major responsibilities of the Medtronic Regulatory Affairs Specialist include:
- Prepare, review and file premarket documentation for global product registrations.
- Support marketing authorization activities with business-unit and international regulatory affairs teams.
- Review pre-clinical and clinical protocols and reports intended for regulatory submissions.
- Develop regulatory strategies for new and modified products.
- Monitor changes in the regulatory environment and assess their potential impact.
- Maintain oral and written communications with health authorities.
- Prepare internal regulatory documentation for device modifications.
- Compile documentation required for submissions, license renewals and annual registrations.
- Participate in health-agency inspections and notified-body audits when required.
- Author and review regulatory procedures and update them when necessary.
- Review change-control documentation and determine regulatory impact.
- Support development and maintenance of regulatory files, records and reporting systems.
- Review promotional materials, advertising and labeling for regulatory compliance.
- Support regulatory clearance and approval requirements for raw materials and prototypes.
- Work with cross-functional teams to address regulatory requirements and project timelines.
Eligibility Criteria
Candidates applying for this Regulatory Affairs Specialist job at Medtronic should meet the following requirements:
Educational Qualification
A bachelor’s degree in one of the following areas or a related healthcare discipline is preferred:
- Medical
- Mechanical Engineering
- Electrical Engineering
- Life Sciences
- Other healthcare-related disciplines
Experience
Candidates should generally have 4–7 years of experience in Regulatory Affairs, particularly within:
- Medical device regulatory affairs
- Pharmaceutical regulatory affairs
- Healthcare technology
- Product registration
- Regulatory submissions
The job description indicates that a combination of medical device and pharmaceutical regulatory experience may be considered.
Required Skills
Important skills for this Medtronic Regulatory Affairs position include:
- Regulatory Affairs
- Medical Device Regulations
- Pharmaceutical Regulations
- Global Regulatory Affairs
- US FDA Regulations
- European Union Regulatory Requirements
- India Regulatory Requirements
- Regulatory Strategy
- Regulatory Submissions
- Product Registration
- Health Authority Communication
- Change Control
- Regulatory Impact Assessment
- Labeling Compliance
- Promotional Material Review
- Clinical and Pre-clinical Documentation
- Project Management
- Cross-functional Collaboration
- Documentation Management
- Written and Verbal Communication
- Attention to Detail
Candidates should also be comfortable interpreting international regulatory requirements and working in a dynamic, cross-functional environment.
Regulatory Knowledge Required
A key requirement for this role is an understanding of regulatory requirements and policies applicable to India, the US FDA and the European Union.
Professionals with experience in global regulatory affairs, international submissions and medical device regulations may find their previous experience relevant to the position.
Salary and Benefits
Medtronic’s supplied job description does not disclose a specific salary range for this position.
For informational purposes only, a market-based estimated range of approximately ₹8 lakh–₹14 lakh per annum may be used for this 4–7-year Regulatory Affairs position in Hyderabad. Actual compensation can vary substantially based on experience, specialization, internal level and Medtronic’s compensation structure.
The job posting states that Medtronic offers a competitive salary and flexible benefits package. The position is also eligible for the Medtronic Incentive Plan (MIP), a short-term incentive.
Medtronic’s careers information also describes opportunities for career development, mentoring, leadership development and learning resources.
Important: The salary estimate above is not an employer-confirmed figure and should not be interpreted as an official Medtronic salary disclosure.
Why Consider a Regulatory Affairs Career at Medtronic?
This position provides exposure to regulatory activities associated with healthcare technology and product development. The Hyderabad Engineering & Innovation Center supports global Medtronic operations across areas including product development, quality and regulatory functions.
The role can also involve interaction with multiple organizational functions, international regulatory teams and health authorities, making cross-functional communication an important component of the position.
Work Location
Nanakramguda, Hyderabad, Telangana, India
The position is listed as Full Time with a Flexible Work Arrangement.