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Quality Control Inspector
Career Insights for Quality Control Analyst
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Based on California data
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What they do
A Quality Control Analyst, in the biotech and medical device industries, works in laboratories performing biological, microbiological, and chemical tests on products and materials. Responsible for calibrating equipment, inspecting products, processing and testing materials, and reporting results. May work in other production environments to monitor and improve quality and efficiency in production systems and products.
$67,470 / year median in California
-12% projected decline
Job Description
- Perform incoming, in-process, and final inspections on manufactured products and components.
- Review and interpret detailed blueprints, engineering drawings, specifications, and inspection criteria.
- Use precision measuring tools such as calipers, micrometers, and measuring tapes to verify product conformance.
- Identify, document, and communicate product discrepancies, defects, and non-conformances.
- Complete and support NCR and MRR processes in accordance with quality procedures.
- Follow cleanroom requirements, PPE standards, gowning procedures, and quality documentation practices. Compensation and Benefits
Pay:
$24.00 to $26.00 per hour.Job Type:
Direct hire.Location:
Camarillo, CA.Schedule:
Multiple shifts available, including early morning and afternoon starts.- Available start times include 4:00 AM, 4:30 AM, 5:00 AM, 6:00 AM, and 4:00 PM.
- Overtime may be required, including early starts, extended shifts, and weekends based on business needs. Required Qualifications and Skills
- Perform product inspections across incoming, in-process, and final inspection stages.
- Interpret blueprints, engineering drawings, and detailed specifications as part of daily inspection work.
- Use handheld precision measuring tools to verify product quality and dimensional accuracy.
- Support non-conformance documentation, NCR activity, and MRR processes.
- 2+ years of Quality Control Inspector or quality inspection experience in a manufacturing environment.
- Strong ability to read and interpret blueprints, engineering drawings, and technical specifications.
- Hands-on experience using calipers, micrometers, measuring tapes, and other handheld measuring tools.
- Experience with incoming inspection, in-process inspection, and final inspection.
- Familiarity with non-conformance reporting, discrepancy documentation, and corrective quality processes.
- Comfortable working in a cleanroom environment while wearing required PPE and gowning for the full shift.
- High attention to detail, strong documentation accuracy, and the ability to follow established quality procedures.
- Flexible schedule with willingness to work overtime, extended shifts, early starts, and weekends as needed. Preferred Qualifications
- Cleanroom manufacturing experience, preferably in an ISO 7 cleanroom environment.
- Experience in medical device, medical supplies, or regulated manufacturing environments.
- Prior experience supporting quality compliance in a production-focused cleanroom setting.
https:
//e-verify.uscis.gov/web/media/resourcesContents/E-Verify_Participation_Poster_ES.pdf We also consider for employment qualified applicants regardless of criminal histories, consistent with legal requirements, including, if applicable, the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment-qualified applicants with arrest and conviction records, including, if applicable, the San Francisco Fair Chance Ordinance. For Los Angeles, CA applicants: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.Benefits
- Sick Leave
- 401(k) Plans
- Health Insurance
- Dental Insurance