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Quality Engineer

Job in Woodinville, King County, Washington, 98072, USA
Listing for: Radiant Systems Inc
Full Time position
Listed on 2026-01-27
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
  • Engineering
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 38 - 44 USD Hourly USD 38.00 44.00 HOUR
Job Description & How to Apply Below

Please let me know if you are interested or anyone who might be interested.

Client:
Major Medical Device Client

Position:
Quality Engineer I

Duration: 2+ months

Pay Rate: $38.00-$44.00/ Hr


*** THIS IS MANUFACTURING QUALITY ENGINEER, NOT IT SOFTWARE QA ROLE***

_______________________________________________________________

Description
  • Working in this Quality Assurance role, you will attend cross functional Daily Management meetings and represent Quality Assurance following up on blocking issues and implementing counter measures.
  • You will manage the Material Review Board and ensure thorough data-driven documentation of non-conformities and risk-based determination of CAPA.
  • You will review data for trends, manage corrections and corrective action and support Global Supply Chain and business partners as requested.
How You'll Make an Impact
  • Support release of high-quality product by managing the Material Review Board and making risk-based and compliant decisions.
  • Maintain the integrity of the Quality Management System by ensuring investigations are well designed, executed and documented.
  • Provide confidence to internal and external customers by following through on actions, continually improving processes, and promoting quality culture.
  • Demonstrate focus and accountability by attending Daily Management and consistently meeting commitments with timeliness and reliability.
  • Facilitate risk management practices and ensure all quality requirements are satisfied.
What You Bring
  • Bachelor’s degree or equivalent in a related scientific discipline. 0-2+ years experience or equivalent combination of education and experience.
  • Ability to apply GMP / ISO regulations and validation principles in a regulated manufacturing environment preferred.
  • Basic understanding of risk management best practices and regulations for the medical device industry.
  • Quality Engineering, Six Sigma Green Belt Certifications desirable.
  • Skilled in statistical methods, statistical process control and experimental design preferred.
  • Ability to work well in fast paced and cross-functional teams.
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