Quality Inspector I
Integra LifeSciences · Facility, NJ
QualityFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Quality Inspector I performs inspections on medical device components, sub-assemblies, and finished products in accordance with FDA regulations and ISO standards. The role involves conducting receiving, in-process, and first-article inspections, maintaining quality records, and supporting cleanroom operations at a New Jersey manufacturing facility.
What they're looking for
- High school diploma
- QA experience in medical device industry preferred
- Working knowledge of ISO 13485, 21CFR820, FDA QSR, and cGMP preferred
- Proficiency with Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) preferred
- Strong attention to detail, organizational skills, and problem-solving ability
- Ability to work independently with minimal supervision
- Must pass visual acuity test; vision aids permitted if worn during inspections
What you'll be doing
- Perform incoming, in-process, and first-article inspections using measuring and test equipment
- Interpret drawings, specifications, and sampling plans to determine material acceptance or rejection
- Maintain accurate inspection records including Material Certifications and Certificates of Conformance
- Conduct inspections in classified cleanrooms and perform line clearances during manufacturing
- Assist in training new associates on Quality System Regulations and standard operating procedures
Compensation$19.19 - $25.43 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.