MDR / Vigilance Specialist (Medical Device Safety & Surveillance)
Company: Medtronic
Location: Hyderabad, India
Employment Type: Full-Time
Job ID: R50011
Experience Required: 3–6 Years (relevant vigilance / safety experience)
Industry: Medical Devices | Healthcare Technology | Diabetes Care
Job Overview
Medtronic is seeking a skilled MDR / Vigilance Specialist to join its expanding Diabetes business operations in India. This role is critical to ensuring global regulatory compliance, post-market surveillance, and safety reporting for medical devices. The position supports Medtronic’s mission to improve patient outcomes through innovative medical technologies while maintaining the highest standards of regulatory and patient safety compliance.
This opportunity is part of Medtronic’s growing Global Diabetes Capability Center, supporting worldwide safety operations and regulatory reporting requirements.
Key Responsibilities
Medical Device Reporting & Vigilance
Monitor and manage the medical device vigilance and surveillance program, including intake, assessment, processing, follow-up, and closure of adverse event reports.
Ensure timely, accurate, and compliant submission of Medical Device Reports (MDRs), adverse event data, and safety reports in accordance with global regulatory requirements.
Maintain complete and accurate safety documentation to support regulatory inspections and audits.
Adverse Event Analysis & Data Management
Review and analyze clinical and safety databases to extract adverse event data.
Integrate safety data into unified databases to support standardization, internal reporting, and regulatory submissions.
Ensure data quality, consistency, and accuracy in safety summaries and reports.
Regulatory Compliance & Cross-Functional Collaboration
Act as a key liaison between internal stakeholders and external partners to support regulatory reporting obligations.
Participate in protocol development, evaluation, and safety issue resolution to ensure compliance with applicable global regulations.
Support investigations related to safety signals, regulatory inquiries, and potential legal or compliance risks.
Required Qualifications & Experience
Education
Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biomedical Engineering, Nursing, or a related healthcare discipline.
Experience
3–6 years of hands-on experience in medical device vigilance, pharmacovigilance, or safety surveillance.
Experience in handling MDRs, adverse event reporting, and post-market surveillance within a medical device or pharmaceutical organization.
Key Skills & Competencies
Strong understanding of medical device vigilance regulations and global safety reporting standards
Experience with adverse event databases and safety reporting systems
Knowledge of regulatory requirements for MDR, ADE, and post-market surveillance
High attention to detail and strong analytical skills
Excellent written and verbal communication skills
Ability to collaborate effectively across cross-functional and global teams
Strong organizational and documentation management skills
Work Environment & Career Growth
Opportunity to work within Medtronic’s global Diabetes business supporting international markets
Exposure to cutting-edge medical technologies and safety systems
Career growth opportunities within Medtronic or its future Diabetes-focused entity following business separation plans
Compensation & Benefits
Competitive salary aligned with market standards
Comprehensive benefits package supporting health, financial well-being, and work-life balance
Eligibility for the Medtronic Incentive Plan (MIP), a short-term performance-based incentive program
Why Join Medtronic
Medtronic is a global leader in healthcare technology, driven by a mission to alleviate pain, restore health, and extend life. With a workforce of over 95,000 professionals worldwide, Medtronic offers a purpose-driven career where innovation, integrity, and patient safety are at the core of everything we do.
SEO Keywords for Global Reach
MDR Specialist jobs, Medical Device Vigilance India, Medtronic careers Hyderabad, Post Market Surveillance jobs, Medical Device Safety Specialist, Pharmacovigilance Medical Devices, Vigilance jobs India.
Disclaimer
This job description outlines the general nature and level of responsibilities and is not intended to be an exhaustive list of all duties or qualifications. Responsibilities may evolve based on business needs and regulatory requirements.
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