Medtronic is a global leader in healthcare technology, committed to alleviating pain, restoring health, and extending life. With over 95,000 employees worldwide, Medtronic engineers innovative medical solutions to tackle complex health challenges. The company fosters a collaborative, purpose-driven culture, ensuring equitable healthcare access.
📍 Location: Nanakramguda, Hyderabad (Hybrid)
🕒 Job Type: Full-time
📅 Posted: Recently
Detailed Job Description
Key Responsibilities:
- Evaluate and document complaint information in electronic databases.
- Perform follow-ups to gather additional details on medical device complaints.
- Determine reportability to FDA, MEDDEV, and Canadian regulatory agencies.
- Maintain audit-ready documentation per internal policies.
- Collaborate with Technical Services, R&D, Manufacturing, and Quality Assurance teams.
- Analyze trending data and ensure accurate complaint categorization.
- Review risk management documentation related to complaints.
- Interact with healthcare professionals, vendors, and customers as needed.
Required Skills & Qualifications:
✔ Bachelor’s degree in Engineering (SW, EE, ME, Biomedical).
✔ 0-2 years of experience in quality assurance or regulatory affairs (medical/pharma industry preferred).
✔ Strong technical writing and communication skills.
✔ Proficiency in MS Office (Word, Excel, Access, PowerPoint).
✔ Ability to multitask and work in a team environment.
✔ Basic understanding of FDA, MEDDEV, and Canadian medical device regulations (preferred).
Nice-to-Have Skills:
- Experience in medical device development & quality control.
- Knowledge of risk management & failure investigation.
Benefits & Compensation
💰 Competitive salary with Medtronic Incentive Plan (MIP).
🏥 Flexible benefits package (health, wellness, retirement).
🌍 Global career growth opportunities.
📚 Continuous learning & development programs.
