Quality Assurance Inspector I
Integra LifeSciences · Facility, UT
QualityFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Quality Assurance Inspector position at a medical device manufacturer responsible for inspecting raw materials, in-process assemblies, and finished goods to ensure compliance with regulatory standards and specifications. Role involves documentation, nonconformity reporting, and collaboration with quality and production teams.
What they're looking for
- 1-5 years quality inspection or similar experience in medical device, pharmaceutical, or regulated manufacturing
- Knowledge of ISO 13485, FDA 21 CFR 820, and Good Manufacturing Practices
- Proficiency interpreting technical drawings, specifications, and work instructions
- Strong attention to detail and documentation capabilities
- Microsoft Office and electronic quality management systems proficiency
- Effective cross-departmental communication and collaboration skills
What you'll be doing
- Conduct incoming inspections of raw materials and components for specification compliance
- Perform in-process inspections to verify assemblies meet quality and regulatory standards
- Inspect finished goods post-sterilization and verify labels and packaging for regulatory compliance
- Document nonconformities and participate in root cause analysis and corrective actions
- Maintain complete inspection records and support continuous improvement initiatives
Compensation$16.68 - $22.12 USD hourly
Privacy & handoff
This role links to Integra LifeSciences's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.