Quality Engineer Ii

Integer

Plymouth, MN, United States
Base: $77,570 - $113,740; bonus/equity: cash-based...
Quality system requirements adherence
Medical device manufacturing compliance
Regulatory and standards compliance
The primary purpose of this job is to provide Quality Engineering support for Operations to ensure that the Quality System requirements are adhered to for medical device manufacturing/operations in accordance with applicable Regulatory and Standards requirements for compliance

Job Summary

  • The primary purpose of this job is to provide Quality Engineering support for Operations to ensure that the Quality System requirements are adhered to for medical device manufacturing/operations in accordance with applicable Regulatory and Standards requirements for compliance.
  • Lead generation and completion of protocols and reports for test method validations and interfaces with Manufacturing Engineers to review processes for new and existing products.
  • Our total rewards program is designed to attract, retain, and motivate associates to contribute to Integer’s success, including a comprehensive benefits package with immediate eligibility.

Matching Summary

The primary purpose of this job is to provide Quality Engineering support for Operations to ensure that the Quality System requirements are adhered to for medical device manufacturing/operations in accordance with applicable Regulatory and Standards requirements for compliance.

Salary

Base: $77,570 - $113,740; Bonus/Equity: Cash-based incentive program; Benefits: Comprehensive benefits package

Skills & Requirements

Must-have

  • Quality System Requirements Adherence
  • Medical Device Manufacturing Compliance
  • Regulatory and Standards Compliance
  • Device History Record Maintenance
  • Non-conforming Material Disposition
  • Continuous Improvement Projects

Nice-to-have

  • Team Collaboration and Communication
  • Independent Work Ethic
  • Time Management Skills
  • Mentoring and Support

Key Requirements

  • Bachelor’s Degree in Engineering or related field
  • 2-5 years quality engineering experience
  • Medical device or regulated manufacturing experience
  • Proficiency in Microsoft Office and Minitab

Work Rights

Not specified

Tailored Resume

Cover Letter