{"schemaVersion":"jobsearcher.job.v1","id":"d74aba4056aa98365fe5f00a","url":"https://jobsearcher.com/jobs/d74aba4056aa98365fe5f00a","canonicalUrl":"https://jobsearcher.com/jobs/d74aba4056aa98365fe5f00a","title":"Lead, Q.C. 1st Shift","description":"Lead and support Quality Inspectors in daily inspection activities and quality-related decision making.\nTrain and qualify inspectors on inspection methods, GMP requirements, documentation practices, and quality procedures.\nMonitor line components, part numbers, documentation, traceability, and compliance with approved specifications.\nPerform and verify in-process inspections including weights, code verification, label verification, functionality testing, appearance inspections, and other required quality checks.\nVerify components against Bills of Materials (BOMs), approved standards, and manufacturing documentation.\nPerform, review, and document required inspections, tests, and measurements.\nAssist Production and Quality Management in troubleshooting manufacturing and quality issues.\nEnsure nonconforming materials and products are properly identified, segregated, documented, and escalated for disposition.\nSupport investigations related to customer complaints, deviations, nonconformances, and corrective actions.\nCoordinate customer sample submissions, approvals, and shipment activities.\nGenerate, review, and upload quality documentation through customer portals, including COAs, COCs, customer questionnaires, product approval documentation, and investigation responses.\nMonitor customer portals and ensure required actions, approvals, and documentation are completed within established timelines.\nSupport customer, corporate, FDA, and third-party audits by providing documentation and responding to requests.\nMonitor quality trends and communicate issues and improvement opportunities to Quality Management.\nPerform additional duties as directed by supervisor.\nEqual Opportunity Employer\nThis employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.","company":"Plz","rawCompany":"plz","city":"Riverside","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-08-03T17:12:09.161Z","occupations":[{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"51-9061.00","title":"Inspectors, Testers, Sorters, Samplers, and Weighers","slug":"inspectors-testers-sorters-samplers-and-weighers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325998","title":"All Other Miscellaneous Chemical Product and Preparation Manufacturing","slug":"all-other-miscellaneous-chemical-product-and-preparation-manufacturing"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Lead, Q.C. 1st Shift","description":"Lead and support Quality Inspectors in daily inspection activities and quality-related decision making.\nTrain and qualify inspectors on inspection methods, GMP requirements, documentation practices, and quality procedures.\nMonitor line components, part numbers, documentation, traceability, and compliance with approved specifications.\nPerform and verify in-process inspections including weights, code verification, label verification, functionality testing, appearance inspections, and other required quality checks.\nVerify components against Bills of Materials (BOMs), approved standards, and manufacturing documentation.\nPerform, review, and document required inspections, tests, and measurements.\nAssist Production and Quality Management in troubleshooting manufacturing and quality issues.\nEnsure nonconforming materials and products are properly identified, segregated, documented, and escalated for disposition.\nSupport investigations related to customer complaints, deviations, nonconformances, and corrective actions.\nCoordinate customer sample submissions, approvals, and shipment activities.\nGenerate, review, and upload quality documentation through customer portals, including COAs, COCs, customer questionnaires, product approval documentation, and investigation responses.\nMonitor customer portals and ensure required actions, approvals, and documentation are completed within established timelines.\nSupport customer, corporate, FDA, and third-party audits by providing documentation and responding to requests.\nMonitor quality trends and communicate issues and improvement opportunities to Quality Management.\nPerform additional duties as directed by supervisor.\nEqual Opportunity Employer\nThis employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.","datePosted":"2026-08-03T17:12:09.161Z","dateModified":"2026-08-03T17:12:09.161Z","hiringOrganization":{"@type":"Organization","name":"Plz","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Riverside","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"d74aba4056aa98365fe5f00a"},"url":"https://jobsearcher.com/jobs/d74aba4056aa98365fe5f00a"}}