Quality Engineer Ii

CyberJobsHub

Plymouth, MN, United States
Base: $77,570 - $113,740; bonus/equity: cash-based...
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Quality management systems compliance
Regulatory and standards knowledge
Product and process validation
** CyberJobsHub is seeking a Quality Engineer II in Plymouth, MN, to ensure compliance with quality system requirements for medical device manufacturing. The role requires oversight of quality engineering processes and mentorship of technicians, focusing on regulatory compliance and continuous improvement. **

Job Summary

  • The role supports operations by ensuring adherence to Quality System requirements for medical device manufacturing in compliance with regulatory standards.
  • The compensation program includes base salary, cash-based incentives, comprehensive benefits, and immediate eligibility for 401(k) with company match.
  • Integer fosters a culture based on core values such as customer focus, innovation, collaboration, inclusion, candor, and integrity.

Matching Summary

Match Score: 75

** CyberJobsHub is seeking a Quality Engineer II in Plymouth, MN, to ensure compliance with quality system requirements for medical device manufacturing. The role requires oversight of quality engineering processes and mentorship of technicians, focusing on regulatory compliance and continuous improvement. **

Salary

Base: $77,570 - $113,740; Bonus/Equity: Cash-based incentive program; Benefits: Medical, dental, vision, disability, life insurance, adoption benefits, parental leave, 401(k) with company match, paid time off

Skills & Requirements

Must-have

  • Quality Management Systems compliance
  • Regulatory and standards knowledge
  • Product and process validation
  • Statistical quality control application
  • Complaint investigation leadership
  • Inspection procedure development
  • Team mentoring and support

Nice-to-have

  • Effective written and verbal communication
  • Ability to work independently and in teams
  • Time management skills
  • Continuous improvement participation
  • Collaboration with cross-functional teams
  • Customer-focused mindset
  • Adherence to company core values

Key Requirements

  • Bachelor’s Degree in Engineering or related field
  • 2-5 years quality engineering experience
  • Experience in medical device or regulated manufacturing
  • Knowledge of ISO, QSR, UL, MDD, TGA regulations
  • Proficiency in Microsoft Office and Minitab

Work Rights

Not specified

Tailored Resume

Cover Letter