Senior Quality Engineer

Integer Holdings Corporation

Base: $114,675 - $168,190; bonus/equity: cash-base...
Bachelor's degree in engineering
7+ years progressive engineering experience
6 sigma green belt certification minimum
The primary purpose of this job is to apply intensive and diversified knowledge of engineering principles to ensure the production of quality products for medical device OEMs

Job Summary

  • The primary purpose of this job is to apply intensive and diversified knowledge of engineering principles to ensure the production of quality products for medical device OEMs.
  • You will lead continuous improvement projects, product transfers, and manage plant CAPA activities including root cause analysis and complaint investigations.
  • The company offers a comprehensive benefits package with immediate eligibility for medical, dental, vision, disability, life insurance, and a 401(k) plan with matching contributions.

Matching Summary

The primary purpose of this job is to apply intensive and diversified knowledge of engineering principles to ensure the production of quality products for medical device OEMs.

Salary

Base: $114,675 - $168,190; Bonus/Equity: Cash-based incentive program included; Benefits: Medical, dental, vision, disability, life insurance, 401(k) match

Skills & Requirements

Must-have

  • Bachelor's degree in engineering
  • 7+ years progressive engineering experience
  • 6 Sigma Green Belt certification minimum
  • ISO QSR FDA regulatory knowledge
  • Process capability studies Cpk DOE
  • Device History Record maintenance
  • Non-conforming material disposition

Nice-to-have

  • Master's degree in engineering field
  • Six Sigma Black Belt preferred
  • Supervision of up to 3 engineers
  • 5 Sigma journey participation
  • Hoshin Plan strategy alignment
  • Cross-functional collaboration skills
  • Positive can-do attitude

Key Requirements

  • Bachelor's degree in engineering or related field
  • 7+ years of progressive engineering experience
  • 6 Sigma Green Belt certification required
  • Knowledge of ISO QSR FDA regulations
  • US work authorization implied by EEO statement

Work Rights

Not specified

Tailored Resume

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