Senior Quality Engineer

Medtronic UK

Tempe, United States
Base: $96,800.00 - $145,200.00; bonus/equity: mip ...
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Quality standards and protocol development
Process development and validation
Statistical analysis and doe
** Medtronic UK is seeking a Senior Quality Engineer for its Tempe, United States location, focusing on the quality and compliance of manufacturing processes for implantable medical devices. The role emphasizes collaboration, process development, and adherence to quality standards in a dynamic and innovative environment. **

Job Summary

  • In this exciting role as a Senior Quality Engineer you will have responsibility for the Quality and Compliance of process development and manufacturing of implantable Cardiac and Neuromodulation medical device related products at Medtronic’s Tempe Campus.
  • Supports manufacturing development and continuous improvement as the Quality team member for process development and validation including Equipment Development, IQ, Process Development (characterization), OQPQ and Test Method Development and Validation.
  • Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values.

Matching Summary

Match Score: 75

** Medtronic UK is seeking a Senior Quality Engineer for its Tempe, United States location, focusing on the quality and compliance of manufacturing processes for implantable medical devices. The role emphasizes collaboration, process development, and adherence to quality standards in a dynamic and innovative environment. **

Salary

Base: $96,800.00 - $145,200.00; Bonus/Equity: MIP eligible; Benefits: Health, Dental, vision, HSA, FSA, Life insurance, Long-term disability, Dependent daycare, Tuition assistance, Simple Steps, 401(k) with match, Short-term disability, PTO, Paid holidays, ESPP, EAP, Non-qualified Retirement Plan Supplement, Capital Accumulation Plan

Skills & Requirements

Must-have

  • Quality standards and protocol development
  • Process development and validation
  • Statistical analysis and DOE
  • Risk assessment processes
  • CAPA investigations

Nice-to-have

  • Electronics manufacturing experience
  • Six Sigma or Lean Sigma certification
  • Medical device audits experience
  • General quality principles understanding

Key Requirements

  • 4 years of relevant experience in Engineering and/or Quality OR Master's degree with 2 years relevant experience OR PhD with 0 years relevant experience
  • Baccalaureate degree in Engineering, Science or technical field

Work Rights

Must have unrestricted US work authorization

Tailored Resume

Cover Letter