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Quality Control Inspector

Job in Anaheim, Orange County, California, 92807, USA
Listing for: Kinetic Personnel Group
Full Time position
Listed on 2026-11-04
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, Production QC/QA
Job Description & How to Apply Below
Job Description

Job Description

Hours: 6:30 am
-3:00 pm Full time

We are seeking an experienced Quality Control Inspector with CMM experience to support a Quality Assurance team in a regulated medical device manufacturing environment. This position performs receiving, in-process, final, and First Article inspections while ensuring products meet engineering specifications, quality standards, and regulatory requirements.

Key Responsibilities

  • Perform dimensional, visual, and functional inspections of components, assemblies, and finished products.
  • Perform Receiving Inspection, First Article Inspection (FAI), and in-process/final inspections.
  • Operate inspection equipment including CMM, Optical Comparator, calipers, micrometers, and gauges.
  • Read and interpret engineering drawings, specifications, tolerances, and inspection requirements.
  • Identify, document, and segregate nonconforming material and support NCR/MRB activities.
  • Maintain accurate inspection records in accordance with Good Documentation Practices.
  • Verify calibration status of inspection equipment before use.
  • Provide technical guidance and training to other QC Inspectors.
  • Support Quality, Engineering, Purchasing, and Production with inspection and continuous improvement activities.

Qualifications

  • High school diploma/GED and 3–5 years of quality inspection experience in an FDA- and ISO-regulated industry.
  • Medical device or electromechanical manufacturing experience strongly preferred.
  • Hands-on CMM and Optical Comparator experience required.
  • Strong understanding of engineering drawings, tolerances, inspection methods, and measurement equipment.
  • Working knowledge of GMP, GDP, FDA 21 CFR Part 820, and ISO 13485.
  • Quality Inspector certification is a plus.
  • Strong attention to detail, documentation skills, and ability to work independently.
  • Apply today to be considered for this opportunity with our client in the medical device manufacturing industry.
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