Quality Engineer Ii

Medtronic Diabetes

Base: $79,200.00 - $118,800.00 usd; bonus: eligibl...
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Bachelor's degree in engineering or science
2 years relevant experience in engineering or quality
Perform complaint investigations for medical devices
** Medtronic Diabetes is seeking a Quality Engineer II to support its Cardiac Ablation Solutions team, focusing on product quality, safety, and reliability through post-market activities. The ideal candidate will possess relevant engineering or quality experience, with a strong emphasis on collaboration and data-driven decision-making in a healthcare technology environment. **

Job Summary

  • This role supports the development and continuous improvement of procedures, processes, tools, and techniques used for product analysis and returned product evaluation.
  • The position contributes to building organizational capability by providing training to technicians and strengthening consistent, compliant execution of quality practices.
  • Medtronic offers a competitive salary range of $79,200.00 - $118,800.00 along with a comprehensive benefits package including health insurance and 401(k) matching.

Matching Summary

Match Score: 75

** Medtronic Diabetes is seeking a Quality Engineer II to support its Cardiac Ablation Solutions team, focusing on product quality, safety, and reliability through post-market activities. The ideal candidate will possess relevant engineering or quality experience, with a strong emphasis on collaboration and data-driven decision-making in a healthcare technology environment. **

Salary

Base: $79,200.00 - $118,800.00 USD; Bonus: Eligible for Medtronic Incentive Plan (MIP); Benefits: Health, Dental, Vision, 401(k), PTO, Tuition Assistance

Skills & Requirements

Must-have

  • Bachelor's degree in Engineering or Science
  • 2 years relevant experience in Engineering or Quality
  • Perform complaint investigations for medical devices
  • Apply statistical methodologies to product performance
  • Devise inspection and testing methods for returned products

Nice-to-have

  • Medical device industry experience
  • Familiarity with FDA 21 CFR Part 820 regulations
  • Knowledge of ISO 13485 and ISO 14971 standards
  • Experience with EU MDR (EU 217/745) regulations
  • Strong written and verbal communication skills

Key Requirements

  • Minimum 2 years relevant experience in Engineering or Quality
  • Bachelor's degree in Engineering, Science, or related technical discipline
  • Unrestricted US work authorization required at time of hire

Work Rights

Must have unrestricted US work authorization

Tailored Resume

Cover Letter