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PHARMA JOBS POST > Medtronic Hiring Regulatory Affairs Specialist in Gurgaon | Apply Online 2026

Medtronic Hiring Regulatory Affairs Specialist in Gurgaon | Apply Online 2026

Apply for Regulatory Affairs Specialist job at Medtronic in Gurgaon, Haryana. Check eligibility, experience, responsibilities, and application details for this full-time healthcare career opportunity.

ADMIN
Last updated: May 14, 2026 2:12 am
ADMIN 2 minutes ago
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Medtronic Hiring Regulatory Affairs Specialist in Gurgaon
Medtronic Hiring Regulatory Affairs Specialist in Gurgaon
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  • Gurgaon, Haryana, India
  • Posted 2 minutes ago
Medtronic

Medtronic

Medtronic Hiring Regulatory Affairs Specialist in Gurgaon

Medtronic has announced an exciting opportunity for the position of Regulatory Affairs Specialist at its Gurgaon, Haryana location. Candidates with a bachelor’s degree and relevant regulatory affairs experience can apply for this full-time role in the healthcare and medical devices industry.

About Medtronic

Medtronic Official Website is one of the world’s leading healthcare technology companies focused on improving patient care through innovative medical solutions. The company offers excellent career growth, global exposure, and opportunities to work on impactful healthcare technologies.


Job Details

Particulars Details
Company Name Medtronic
Post Name Regulatory Affairs Specialist
Job Location Gurgaon, Haryana, India
Job Type Full Time
Job Requisition ID R66375
Experience Required Minimum 2 Years
Qualification Bachelor’s Degree / Advanced Degree
Industry Medical Devices / Healthcare

Job Responsibilities

Selected candidates will be responsible for:

  • Coordinating and preparing document packages for regulatory submissions
  • Managing internal audits and inspections
  • Compiling materials required for submissions, renewals, and annual registrations
  • Recommending changes related to labeling, manufacturing, marketing, and clinical protocols
  • Monitoring and improving tracking and control systems
  • Staying updated with changing regulatory procedures and compliance requirements
  • Interacting with regulatory agencies on assigned matters
  • Supporting strategies for faster approvals of clinical trial applications
  • Managing assigned projects while coordinating with multiple stakeholders

Required Skills & Experience

Candidates should possess:

  • Bachelor’s degree or equivalent qualification
  • Minimum 2 years of relevant experience in Regulatory Affairs
  • Strong knowledge of regulatory submission processes
  • Good communication and coordination skills
  • Ability to work independently on moderately complex projects
  • Knowledge of healthcare or medical device regulations preferred

Key Highlights

  • Opportunity to work with a globally recognized healthcare company
  • Exposure to regulatory affairs in the medical devices industry
  • Career growth and learning opportunities
  • Collaborative and innovation-driven work environment

How to Apply

Interested and eligible candidates can apply online through the official Medtronic careers portal.

👉 Apply Here

To apply for this job please visit medtronic.wd1.myworkdayjobs.com.

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By ADMIN
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Sanyasi Pradhan, M.Pharm, is a pharma professional and entrepreneur with a strong background in the pharmaceutical industry, writing on jobs and global pharma updates
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