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Quality Control Inspector in Camarillo

Job in Camarillo, Ventura County, California, 93012, USA
Listing for: Energy Jobline ZR
Full Time position
Listed on 2026-10-15
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, Production QC/QA
Salary/Wage Range or Industry Benchmark: 55000 - 75000 USD Yearly USD 55000.00 75000.00 YEAR
Job Description & How to Apply Below

Job Description Job Description

Immediate Opening! Quality Control Inspector

We are seeking a highly detail-oriented Quality Control Inspector to test and inspect materials, parts, and products at various stages of production. This role is ideal for a dedicated quality professional with a strong background in pharmaceutical or medical device regulations, meticulous documentation habits, and a collaborative approach to continuous improvement.

Key Responsibilities
  • Perform incoming, first article, in-process, and final inspections to ensure full compliance with company and regulatory standards
  • Initiate nonconformance reports (NCR) for any non-conforming materials identified during operations
  • Review, complete, and release manufacturing job order documents using Good Documentation Practices (GDP)
  • Approve or reject raw materials based on established quality standards and communicate findings to all required parties
  • Support cross-functional investigations into non-conformance findings and provide recommendations for process improvements
  • Perform critical pre- and post-inspection steps for products undergoing the gamma irradiation process
  • Compile quality metrics data and regularly submit structured reports to the QC Supervisor or Lead
  • Maintain a safe, orderly workspace and wear full personal protective equipment (PPE) including scrubs, coveralls, masks, and eyewear in an ISO cleanroom environment
Qualifications
  • High School Diploma or equivalent required
  • Minimum 3 years of experience in manufacturing quality control inspections
  • At least 1 year of experience handling technical documentation and corrective actions in a pharmaceutical or medical device setting
  • Working knowledge of global regulations, including ISO 9001, ISO 13485, and 21 CFR Parts 210, 211, or 820
  • Proven ability to execute strict GMP operations by following detailed Standard Operating Procedures (SOPs)
  • Hands-on experience using precision measuring devices such as calipers, rulers, tape measures, and pin gauges
  • Solid basic mathematics, computer proficiency, and working knowledge of ERP systems (such as Syte Line)
  • Strong interpersonal and communication skills to effectively collaborate across internal departments and external vendors
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