Quality Control Inspector in Camarillo
Job in
Camarillo, Ventura County, California, 93012, USA
Listed on 2026-10-15
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
Job Description & How to Apply Below
Job Description Job Description
Immediate Opening! Quality Control InspectorWe 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
- 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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