Medtronic Hiring Pharmacovigilance Specialist
- MDR/Vigilance Specialist – Medtronic – Hyderabad
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Summary Table
- FAQs
MDR/Vigilance Specialist – Medtronic – Hyderabad
Apply for Medtronic’s MDR/Vigilance Specialist role in Hyderabad. Full-time opportunity for experienced professionals in medical device vigilance.
Medtronic is expanding its Global Diabetes Capability Center and inviting skilled professionals to contribute to safety vigilance and regulatory reporting for advanced diabetes technologies. This role supports global safety operations and plays a key part in ensuring product compliance, patient protection, and regulatory excellence.
Company Overview
Medtronic is a global leader in healthcare technology, focused on creating solutions that advance patient outcomes and transform disease management. With a legacy of innovation, the organization brings together engineering, clinical expertise, and advanced science to tackle humanity’s most challenging health issues. The Hyderabad site supports global vigilance operations for the Diabetes division, contributing to safety excellence across medical devices and digital health solutions.
Job Role & Responsibilities
As an MDR/Vigilance Specialist, you will support end-to-end device vigilance operations and regulatory compliance activities. Key responsibilities include:
- Monitoring and managing medical device surveillance activities.
- Handling intake, evaluation, processing, and follow-up of adverse event reports.
- Ensuring accuracy and completeness in Medical Device Reports (MDRs), Adverse Drug Experience (ADE) data, and adverse reaction documentation.
- Reviewing clinical databases to identify ADE information and ensuring consistency and quality of safety summaries.
- Collaborating with internal and external stakeholders to maintain compliance with regulatory reporting standards.
- Supporting protocol development, regulatory submissions, and documentation maintenance.
Eligibility / Qualifications
- Bachelor’s degree in Life Sciences, Pharmacy, Biomedical Engineering, Nursing, or a related field.
- Experience in pharmacovigilance, medical device vigilance, or safety case processing preferred.
- Strong analytical abilities with understanding of safety databases and regulatory reporting.
- Ability to review clinical data, identify safety signals, and ensure compliance with global reporting requirements.
- Excellent communication and documentation skills.
Location & Salary
- Location: Hyderabad, Andhra Pradesh
- Type: Full-time
- Compensation: Competitive salary with performance-based incentives (Medtronic Incentive Plan) and a comprehensive benefits package.
Application Process
Interested candidates can review the full posting and apply through the official Medtronic career portal:
Apply Here
Summary Table
| Company | Medtronic |
|---|---|
| Vacancies | Not specified |
| Required Education | Life Sciences, Pharmacy, Biomedical Engineering, Nursing |
| Experience | Prior experience in PV or medical device vigilance preferred |
FAQs
1. Who is eligible for the MDR/Vigilance Specialist role?
Candidates with a background in life sciences, pharmacy, or medical technology and experience in safety or regulatory operations are preferred.
2. Is this a device-focused pharmacovigilance role?
Yes. The role focuses primarily on medical device vigilance, MDR reporting, and adverse event evaluation.
3. Does Medtronic offer growth opportunities?
Medtronic provides structured career development, competitive compensation, and opportunities to work on global healthcare technologies.
4. Where is the job located?
The position is based in Hyderabad, supporting global Diabetes division operations.
5. How do I apply?
Submit your application through the official link provided above.
To apply for this job please visit medtronic.wd1.myworkdayjobs.com.
