Hiring: Quality Engineer | Chicago, IL
Seeking a Quality Engineer to support a leading medical supply client with quality remediation and compliance initiatives.
• 3–5+ years of experience in Medical Devices, Pharmaceuticals, or regulated Healthcare Manufacturing
• Strong knowledge of 21 CFR Part 820 and/or ISO 13485
• Experience with DMRs, DHFs, Design Controls, Risk Management, and CAPA processes
• Familiarity with Reliance or similar QMS platforms
• Support DHF remediation, audit readiness, change control, and quality system improvements
• Collaborate with R&D, Regulatory Affairs, Manufacturing, and Supplier Quality teams
• Strong problem-solving, communication, and time-management skills
Interested candidates can share their resume at laxmiprasanna@intellectt.com or reach out directly for more information.