Quality Engineer Ii

OnboardNWA

Base: $77,570- $113,740; bonus/equity: cash-based ...
Quality management systems compliance
Regulatory and standards adherence
Quality engineering tools and techniques
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.
  • Our total rewards program is designed to attract, retain, and motivate associates to contribute to Integer’s success and includes base salary, cash-based incentives, and a comprehensive benefits package with immediate eligibility.
  • Employees are immediately eligible to participate in the 401(k) plan with company matching contributions and receive 80 hours of company designated holidays plus an annual allotment of paid time off.

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: Medical, dental, vision, disability, life insurance, adoption benefits, parental leave, 401(k) with company match

Skills & Requirements

Must-have

  • Quality Management Systems compliance
  • Regulatory and standards adherence
  • Quality Engineering tools and techniques
  • Deviation and waiver guidance
  • Process validation coordination
  • Complaint investigations leadership
  • Statistical quality control application

Nice-to-have

  • Team mentoring and support
  • Effective written and verbal communication
  • Time management skills
  • Continuous improvement participation
  • Collaboration with cross-functional teams
  • Knowledge of domestic and international regulations

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 FDA regulations and ISO standards

Work Rights

Not specified

Tailored Resume

Cover Letter