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Quality Engineer

Job

Hired by Matrix, Inc.

Remote

$139,360 Salary, Full-Time

Posted 03/11/2026 (Updated 8 weeks ago) • Actively hiring

Expires 5/27/2026

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Job Description

Quality Engineer#26-01016 $0-$67 per hour Chicago, IL
Fully Remote Job Description At-a-Glance:
Are you ready to build your career by joining a certified technology solutions and compliance consulting services company? If so, our client is hiring a Quality Engineer.
Position Type:
Contract Remote
Required:
Bachelor's degree in a technical/scientific discipline; Master's or PhD experience beneficial. 2-5 years of experience in Quality Systems within regulated industries, preferably medical devices. Knowledge of GMP, GLP, ISO, Six Sigma, Root Cause Analysis, and statistical analysis Strong understanding of microbiology, molecular biology, biochemistry, chemistry, and related laboratory/manufacturing sciences. Proven ability to plan, execute, and supervise projects, including risk assessment, CAPAs, and technical investigations. Excellent technical writing, analytical, and problem-solving skills, with experience documenting investigations, reports, and process improvements. Ability to work in controlled environments, clean rooms, high-voltage electronics, and radiation areas, while collaborating effectively across teams.
Responsibilities:
Design, implement, and maintain quality assurance protocols for materials, partially finished, and finished products. Lead and execute moderate to complex projects, including Change Orders (ECOs), CAPAs, Non-Conformance Events (NCE), and product/process investigations. Write, execute, and coach others on PQs, TMVs, and simple procedure updates, ensuring team adherence to quality standards. Perform risk management, defect investigations, and root cause analyses, providing sustainable corrective actions and preventive measures. Collaborate with Operations, Engineering, and R D to ensure regulatory and quality compliance across all processes, products, and documentation. Author and review technical protocols, reports, and quality documentation, maintaining compliance with QMS, FDA, ISO, and Medical Device Directive requirements. Analyze production data and large datasets, identify trends, recommend process improvements, and mentor junior engineering staff in quality best practices. Get in
Touch:
We want to hear from you! If you think you'd be a good match, submit your resume and reach out to Vaibhav at 551-227-9117 to learn more. #LI-VK1 #HbM6349

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