Quality Engineer
Intellectt Inc
• 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
Vacancy posted 1 day ago
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