Quality Engineer Iii

Integer

Plymouth, MN, United States
Base: $93,225 - $136,730; bonus/equity: cash-based...
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Quality management systems compliance
Regulatory and agency inspection support
Product and process improvement methodologies
** Integer is seeking a Quality Engineer III to join their team in Plymouth, MN, focusing on quality deliverables in medical device manufacturing. The ideal candidate should possess 5-7 years of experience in regulated manufacturing and have a strong background in quality engineering tools and techniques. **

Job Summary

  • Integer is a global organization providing innovative, high-quality technologies and manufacturing to Medical Device OEMs to enhance the lives of patients worldwide.
  • The role involves supporting product development projects, ensuring compliance with quality systems and regulatory requirements, and leading quality improvement initiatives.
  • The company offers a comprehensive benefits package including medical, dental, vision, disability, life insurance, 401(k) with matching, paid time off, and parental leave.

Matching Summary

Match Score: 75

** Integer is seeking a Quality Engineer III to join their team in Plymouth, MN, focusing on quality deliverables in medical device manufacturing. The ideal candidate should possess 5-7 years of experience in regulated manufacturing and have a strong background in quality engineering tools and techniques. **

Salary

Base: $93,225 - $136,730; Bonus/Equity: Cash-based incentive program; Benefits: Medical, dental, vision, disability, life insurance, 401(k) with matching, paid time off

Skills & Requirements

Must-have

  • Quality Management Systems compliance
  • Regulatory and agency inspection support
  • Product and process improvement methodologies
  • Statistical quality control application
  • Risk analysis and test method validation
  • Manufacturing process monitoring and validation

Nice-to-have

  • Strong communication skills
  • Team collaboration and independent work
  • Knowledge of SPC, FMEA, DOE, RCA, GDT
  • Customer interaction and complaint management
  • Adherence to company values and safety standards

Key Requirements

  • Bachelor’s Degree in Engineering or related field
  • 5-7 years medical device or regulated manufacturing experience
  • Competence in Quality Engineering Tools and Techniques
  • Knowledge of Domestic and International Regulations and Standards
  • Certified Quality Engineering or Six Sigma Green/Black Belt desired

Work Rights

Not specified

Tailored Resume

Cover Letter