{"schemaVersion":"jobsearcher.job.v1","id":"910f8a3ef2c35575ce40a899","url":"https://jobsearcher.com/jobs/910f8a3ef2c35575ce40a899","canonicalUrl":"https://jobsearcher.com/jobs/910f8a3ef2c35575ce40a899","title":"QC Analyst","description":"Job Title: QC Analyst\nLocation: Novato, CA\nType: Contract\nCompensation: $28.00 - $32.00\nWork Model: Onsite – onsite\nHours: Wednesday - Saturday (Onsite 4 days), swing shift (1pm-11:30 pm)\n\nOverview\nLeading biotechnology company looking for an experienced QC Analyst. Ideal candidates should have a bachelors degree and 0-3 years of relevant laboratory experience; QC experience is preferred.\n\nResponsibilities\nFacilitate incoming sample receipt and accessioning flow, decipher batch assignments across all assay types in accordance with best practices.\nExecute analytical methods to facilitate in-process testing under applicable cGMP guidelines, and report results promptly to meet internal deadlines.\nEvaluate assay validity, calculate and summarize results, perform trend analysis, and assist in compiling reports.\nMaintain laboratory cleanliness and ensure systems for laboratory maintenance support inspection readiness.\nMonitor and control laboratory supply and critical reagent inventories.\nQualify and provide training for specific analytical methods to less experienced staff.\nCommunicate proactively regarding compliance risks or deviations, initiate investigation records as needed.\nSupport test method validations, investigations, technical studies, and protocol transfers.\nParticipate in team meetings, suggest improvements for laboratory infrastructure and processes.\nIdentify opportunities to enhance operational efficiency and reduce non-value-added activities.\nPerform other duties as necessary to support laboratory operations.\n\nRequirements\nBachelor of Science degree.\n0-3 years of relevant laboratory experience; QC experience preferred.\nKnowledge of quality management systems, cGMP practices, and QC principles.\nStrong documentation and communication skills (both written and verbal).\nAbility to work independently with minimal supervision.\nProficiency in Microsoft Word and Excel; experience in PowerPoint is a plus.\nFamiliarity with BINOCS or similar scheduling systems is preferred.\nExperience with SAP or similar enterprise systems is advantageous.\nFlexible with additional hours to meet production and laboratory needs.\n\nSystem One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.\n\nSystem One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.\n\nRef: #558-Scientific","company":"Systemone","rawCompany":"systemone","city":"Novato","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-08-11T16:08:59.778Z","occupations":[{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"19-4031.00","title":"Chemical Technicians","slug":"chemical-technicians"}],"industries":[{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"code":"325413","title":"In-Vitro Diagnostic Substance Manufacturing","slug":"in-vitro-diagnostic-substance-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"QC Analyst","description":"Job Title: QC Analyst\nLocation: Novato, CA\nType: Contract\nCompensation: $28.00 - $32.00\nWork Model: Onsite – onsite\nHours: Wednesday - Saturday (Onsite 4 days), swing shift (1pm-11:30 pm)\n\nOverview\nLeading biotechnology company looking for an experienced QC Analyst. Ideal candidates should have a bachelors degree and 0-3 years of relevant laboratory experience; QC experience is preferred.\n\nResponsibilities\nFacilitate incoming sample receipt and accessioning flow, decipher batch assignments across all assay types in accordance with best practices.\nExecute analytical methods to facilitate in-process testing under applicable cGMP guidelines, and report results promptly to meet internal deadlines.\nEvaluate assay validity, calculate and summarize results, perform trend analysis, and assist in compiling reports.\nMaintain laboratory cleanliness and ensure systems for laboratory maintenance support inspection readiness.\nMonitor and control laboratory supply and critical reagent inventories.\nQualify and provide training for specific analytical methods to less experienced staff.\nCommunicate proactively regarding compliance risks or deviations, initiate investigation records as needed.\nSupport test method validations, investigations, technical studies, and protocol transfers.\nParticipate in team meetings, suggest improvements for laboratory infrastructure and processes.\nIdentify opportunities to enhance operational efficiency and reduce non-value-added activities.\nPerform other duties as necessary to support laboratory operations.\n\nRequirements\nBachelor of Science degree.\n0-3 years of relevant laboratory experience; QC experience preferred.\nKnowledge of quality management systems, cGMP practices, and QC principles.\nStrong documentation and communication skills (both written and verbal).\nAbility to work independently with minimal supervision.\nProficiency in Microsoft Word and Excel; experience in PowerPoint is a plus.\nFamiliarity with BINOCS or similar scheduling systems is preferred.\nExperience with SAP or similar enterprise systems is advantageous.\nFlexible with additional hours to meet production and laboratory needs.\n\nSystem One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.\n\nSystem One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.\n\nRef: #558-Scientific","datePosted":"2026-08-11T16:08:59.778Z","dateModified":"2026-08-11T16:08:59.778Z","hiringOrganization":{"@type":"Organization","name":"Systemone","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Novato","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"910f8a3ef2c35575ce40a899"},"url":"https://jobsearcher.com/jobs/910f8a3ef2c35575ce40a899"}}