Quality Assurance Inspector I - Medical Devices

Integra LifeSciences Corporation; Utah; On-site; USD 23,419 - 30,307; Full time

Job summary

Integra LifeSciences Corporation in West Valley City, UT is seeking a Quality Assurance Inspector I to perform incoming, in-process, and finished goods inspections, ensuring compliance with specifications and GDP.

You will review drawings, maintain inspection records, support CAPA activities, and work with QA Engineers and Production to resolve issues; 1–5 years in medical device QC preferred; ISO 13485, FDA 21 CFR 820 familiarity encouraged.

Qualifications

• 1–5 years in quality inspection in medical device or regulated manufacturing.
• Familiarity with ISO 13485, FDA 21 CFR 820, GMP preferred.
• Ability to read drawings and specifications.

Responsibilities

• Conduct incoming inspections of raw materials and components to verify specifications.
• Perform in-process inspections to ensure assemblies meet standards.
• Inspect finished goods from sterilization for final release criteria.
• Verify labels and packaging for regulatory compliance.
• Maintain inspection records per GDP and company policies.
• Support continuous improvement and root cause analysis.

Skills

Inspection techniques

Measurement tools

Technical drawings

Documentation

MS Office & eQMS

Cross-department collaboration

Job description

Integra LifeSciences Corporation in West Valley City, UT is seeking a Quality Assurance Inspector I to perform incoming, in-process, and finished goods inspections, ensuring compliance with specifications and GDP.

You will review drawings, maintain inspection records, support CAPA activities, and work with QA Engineers and Production to resolve issues; 1–5 years in medical device QC preferred; ISO 13485, FDA 21 CFR 820 familiarity encouraged.