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Quality Inspector

Job in Palo Alto, Santa Clara County, California, 94306, USA
Listing for: RecruitGigs
Full Time position
Listed on 2026-03-01
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Quality Control / Manager, Quality Technician/ Inspector
  • Manufacturing / Production
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Our client is a well-established and growing medical device manufacturer located in Palo Alto, CA. They are committed to producing high-quality, precision-engineered products that meet strict regulatory and customer requirements. This is an excellent opportunity to join a collaborative team in a fast-paced, highly regulated environment.

Position Summary

The Senior Quality Inspector is responsible for performing complex inspections of incoming, in-process, and finished medical device components to ensure compliance with internal specifications, customer requirements, and regulatory standards. This role requires strong technical inspection skills, attention to detail, and experience working within FDA-regulated environments.

Key Responsibilities
  • Perform detailed inspection of precision components and assemblies using hand tools and advanced measuring equipment
  • Interpret engineering drawings, GD&T, blueprints, and specifications
  • Conduct first article inspections (FAI) and document results
  • Perform incoming, in-process, and final inspections
  • Ensure compliance with quality system requirements (ISO and FDA standards)
  • Identify nonconforming materials and assist with root cause investigations
  • Support corrective and preventive action (CAPA) activities
  • Maintain accurate inspection records and documentation
  • Train and mentor junior inspectors as needed
  • Collaborate with engineering, manufacturing, and quality teams to resolve quality issues
Qualifications
  • 5+ years of quality inspection experience in medical device or regulated manufacturing
  • Strong knowledge of ISO 13485 and FDA quality system regulations
  • Proficient in reading engineering drawings and GD&T
  • Experience with calipers, micrometers, height gauges, comparators, CMM, and other inspection tools
  • Experience performing First Article Inspections (AS9102 experience is a plus)
  • Strong documentation and organizational skills
  • High attention to detail and problem-solving ability
Preferred Qualifications
  • Associate’s degree or technical certification in Quality, Manufacturing, or related field
  • Experience in cleanroom environments
  • Prior experience mentoring or leading inspection teams
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