Principal Process Engineer

Medtronic

Base: $125,600.00 - $188,400.00; bonus/equity: eli...
Onsite (minimum of 4 days per week)
Value analysis value engineering vave
Regulated industry manufacturing processes
Cross functional team leadership
Medtronic is seeking a Principal Process Engineer to lead projects focused on Value Analysis/Value Engineering (VAVE) for power components across their Cardio and Neuro device platforms. The role requires substantial technical expertise and collaboration with cross-functional teams to optimize product manufacturing in compliance with regulatory standards

Job Summary

  • This engineer will serve as the project lead for the Value Analysis/Value Engineering portfolio focused on power components across Cardio and Neuro device platforms.
  • The role requires leading execution with a cross-functional group including R&D, operations, supply chain, quality, and VAVE while maintaining compliance to Medtronic standards.
  • Medtronic offers a competitive salary range of $125,600.00 - $188,400.00 along with comprehensive benefits including health insurance, 401(k) matching, and incentive plans.

Matching Summary

Match Score: 85

Medtronic is seeking a Principal Process Engineer to lead projects focused on Value Analysis/Value Engineering (VAVE) for power components across their Cardio and Neuro device platforms. The role requires substantial technical expertise and collaboration with cross-functional teams to optimize product manufacturing in compliance with regulatory standards.

Salary

Base: $125,600.00 - $188,400.00; Bonus/Equity: Eligible for Medtronic Incentive Plan (MIP); Benefits: Health, dental, vision, 401(k) match, paid time off

Skills & Requirements

Must-have

  • Value Analysis Value Engineering VAVE
  • Regulated industry manufacturing processes
  • Cross functional team leadership
  • Process validation OQ PQ IQ FAT SAT
  • Statistical analysis and FMEA

Nice-to-have

  • Predictive engineering optimization skills
  • Innovation and new product development
  • Collaborative onsite work culture
  • Fast learning cycle execution

Key Requirements

  • Baccalaureate degree with 7 years experience OR Master's with 5 years OR PhD with 3 years
  • US work authorization required for non-Principal roles
  • Experience in regulated medical device manufacturing

Work Rights

Unrestricted US work authorization required for roles below Principal level

Sponsorship: available

Tailored Resume

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