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Quality Assurance Inspector I

Integra LifeSciences
August 29, 2026
Full-time
On-site
West Valley City, UT
Operations
Role: Quality inspector within regulated manufacturing, focused on raw materials, in-process assemblies, and finished goods to ensure compliance with specifications and regulatory standards. Responsibilities: perform incoming, in-process, and final inspections; verify labels and packaging; review Lot History Records; document nonconformities; collaborate with quality and production teams to resolve issues; support continuous improvement and maintain GMP-compliant records. Requirements: 1-5 years in quality inspection, with familiarity in ISO 13485, FDA 21 CFR 820, and GMP preferred; strong inspection skills, attention to detail, proficiency with measurement tools, technical drawings, and electronic quality management systems. High-Value: medical device/pharmaceutical manufacturing, regulated industry, GMP compliance, minimal travel. WorkSetup: not specified, likely on-site based on environment.