Quality Engineer (Non-Light Industrial
Listed on 2026-08-05
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Quality Assurance - QA/QC
Quality Engineering
Quality Engineer (Non-Light Industrial)
A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas:
Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
Hi [[Candidate First Name ]],
I came across your resume online and found it very impressive. I have an immediate opening with one of my direct client.
Following is the position details. Please let me know if you are available/interested so we can further discuss this position
Job title-Quality Engineer (Non-Light Industrial)
Job location-Franklin lakes, NJ
Duration: 6+ months (possibility of extension)
QUALIFICATIONS:
• Education and Experience BS degree in (Electrical Engineering, Software/Computer Science or similar discipline) and a minimum of 4-5 years of experience in Medical Device/Biotechnology Industry required.
• Professional certification is preferred (i.e. CQA-Certified Quality Auditor, CQE-Certified Quality Engineer, SQE-Software Quality Engineer, CQM
- Certified Quality Manager, etc.).
• SAP experience preferred.
RESPONSIBILITIES:
• The Quality Engineer will be responsible for working closely with other functions within the organization (Manufacturing, R&D, Quality, Engineering, Procurement, and Marketing) and ensuring the quality of the product and processes for the assigned product line(s) are in compliance with standard Quality practices.
• Provide coordination and guidance to cross functional teams to ensure software quality objectives are met for product software, manufacturing software, quality system software, and software technologies included or used in the creation or production of medical devices.
• Demonstrate functional knowledge and expertise in product development, software development, software lifecycle processes, regulatory requirements, international standards, and risk management.
• Responsible for developing, documenting and/or maintaining design history files
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