Medtronic, one of the world’s leading healthcare technology companies, is inviting applications for the position of MDR/Vigilance Specialist at its Hyderabad office. This is an excellent opportunity for professionals with experience in Medical Device Vigilance, Complaint Handling, Quality Assurance, Regulatory Affairs, and MDR Reporting to work with a global medical device leader.

If you have 4–8 years of experience in medical devices or pharmaceutical quality and regulatory affairs, this Medtronic career opportunity offers competitive compensation, flexible work arrangements, performance incentives, and exposure to global regulatory compliance.

Job Highlights

About Medtronic

Medtronic is a global healthcare technology company operating in more than 150 countries with over 95,000 employees worldwide. The company develops innovative medical technologies that improve the lives of more than 72 million patients annually. Medtronic offers outstanding career growth, learning opportunities, and a mission-driven work environment.

MDR/Vigilance Specialist Job Responsibilities

The selected candidate will be responsible for managing medical device complaints and ensuring compliance with global regulatory requirements.

Key responsibilities include:

• Process customer complaints using electronic complaint management systems.
• Evaluate complaint information received from multiple sources.
• Conduct follow-up investigations to collect missing information.
• Determine Medical Device Report (MDR) reportability.
• Submit regulatory reports to government agencies.
• Maintain complaint records in an audit-ready condition.
• Perform complaint trending and database analysis.
• Prepare investigation summaries based on technical findings.
• Coordinate with Technical Services, Manufacturing, Engineering, R&D, and Quality Assurance teams.
• Review risk management documentation related to complaint events.
• Support compliance with FDA, Canadian, and international medical device regulations.
• Communicate with healthcare professionals, customers, and vendors when required.

Required Qualifications

Applicants should possess:

• Bachelor’s degree in Engineering or Science.
• Preferred disciplines include:
  • Biomedical Engineering
  • Electronics & Communication Engineering (ECE)
  • Mechanical Engineering
  • Other relevant Science degrees
• 4–8 years of experience in:
  • Medical Device Vigilance
  • Quality Assurance
  • Regulatory Affairs
  • Complaint Handling
  • Medical Device Reporting (MDR)
  • Pharmaceutical Quality

Preferred Skills

Candidates with the following skills will have an advantage:

• Medical Device Complaint Management
• FDA Medical Device Regulations
• MEDDEV Guidelines
• Canadian Medical Device Regulations
• Technical Writing
• Risk Management Documentation
• Complaint Trending Analysis
• Microsoft Excel
• Microsoft Word
• PowerPoint
• Database Management
• Strong Communication Skills
• Ability to understand complex medical devices
• Team collaboration

Salary (Expected)

Based on industry standards for Hyderabad and similar Medtronic roles:

Estimated Salary: ₹12 LPA – ₹18 LPA

Actual salary may vary depending on experience, skills, and interview performance.

Employee Benefits

Medtronic offers an attractive benefits package including:

• Competitive Salary
• Flexible Work Arrangement
• Medtronic Incentive Plan (Performance Bonus)
• Health Insurance
• Career Development Programs
• Global Learning Opportunities
• Employee Wellness Programs
• International Work Environment
• Paid Leave
• Professional Growth Opportunities

Why Join Medtronic?

Working at Medtronic provides professionals with opportunities to:

• Build a career in global medical device vigilance.
• Gain exposure to international regulatory reporting.
• Work with cutting-edge medical technologies.
• Collaborate with global engineering and quality teams.
• Develop expertise in FDA and international compliance.
• Advance within one of the world’s largest healthcare technology companies.

How to Apply

Application Link