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Regulatory Affairs Openings at Medtronic

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Medtronic

B.Pharm, M.Pharm, Msc, BSc, Lifesciences. Engineering, or related fields.

Hyderabad

1 year+

Verified Job

Online Application
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Medtronic, a global leader in healthcare technology, is inviting applications for the position of Regulatory Affairs Specialist at its Nanakramguda, Hyderabad location. This is a golden opportunity for life science and pharmaceutical professionals passionate about regulatory compliance, global submissions, and medical device innovation.

If youโ€™re ready to engineer the extraordinary, this role offers a chance to work with a global team committed to improving lives and advancing medical technology.


๐Ÿ” Job Overview

Position: Regulatory Affairs Specialist
Company: Medtronic
Location: Nanakramguda, Hyderabad, India
Job Type: Full-time
Date Posted: October 10, 2025
Experience Required: Minimum 1 year in regulatory affairs or related field
Education: Bachelorโ€™s degree in Science, Pharmacy, Engineering, or equivalent
Salary Range: โ‚น6,00,000 โ€“ โ‚น12,00,000 per annum (based on experience)


๐Ÿงฉ Key Responsibilities

As a Regulatory Affairs Specialist at Medtronic, your key responsibilities will include:

  • Preparing and coordinating regulatory submission packages for global and local health authorities.
  • Compiling materials for license renewals, annual registrations, and internal audits.
  • Recommending updates to labeling, manufacturing, marketing, and clinical protocols to ensure compliance.
  • Tracking and improving regulatory documentation systems and submission timelines.
  • Staying updated on the latest regulatory guidelines and best practices.
  • Communicating effectively with cross-functional teams and, when needed, regulatory agencies to support product approvals.
  • Supporting strategies for early clinical trial application approvals.

๐ŸŽ“ Required Qualifications

To succeed in this role, you should have:

  • A Bachelorโ€™s degree in Life Sciences, Pharmacy, Engineering, or related fields.
  • Minimum 1 year of relevant regulatory experience (preferably in medical devices or pharmaceuticals).
  • Strong understanding of regulatory documentation, submission formats, and compliance standards.
  • Excellent communication and coordination skills.
  • Ability to work independently and manage moderately complex projects.

๐Ÿ’ผ Why Join Medtronic?

At Medtronic, employees are empowered to innovate fearlessly and make an impact. Hereโ€™s what you can expect:

  • Competitive Salary and Benefits Package
  • Opportunities for career growth and global exposure
  • Work in a collaborative, purpose-driven culture
  • Access to learning and development resources
  • A chance to contribute to Medtronicโ€™s mission to alleviate pain, restore health, and extend life

๐Ÿ“ How to Apply

Application Link

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