{"schemaVersion":"jobsearcher.job.v1","id":"726b7bb1c105587360ed6053","url":"https://jobsearcher.com/jobs/726b7bb1c105587360ed6053","canonicalUrl":"https://jobsearcher.com/jobs/726b7bb1c105587360ed6053","title":"Formulation Manufacturing Associate","description":"Summary\n\nFormulates oligonucleotide probes, primers and assays (RUO, ASR, EUA & 510K). Manages oligo stocks inventory. Assists Manager in managing RUO, ASR, EUA and 510K products inventory.\n\nEssential Duties and Responsibilities\n\nDissolves and dilutes oligonucleotide synthesis products, analyzes concentration, formulates assays (RUO, ASR, EUA & 510K), prints labels according to specifications and apply labels to product tubes.\nFormulate solutions mixes according to SOPs and Work Sheets (WS) to prepare finished products.\nPrepare and submit oligo samples for Mass Spec analysis.\nManages oligo stocks inventory.\nAssists Director/Manager in managing RUO, ASR, EUA and 510K products inventory.\nManufactures stocks of raw materials and buffers, and maintains lab supplies, etc.\nCalibrates and maintains lab equipment as required.\nMakes inventory corrections and consumptions in NAV.\nWriting manufacturing operating procedures that are technically sound, promote effective and efficient operations, and comply with cGMP requirements. Edit SOP, SEPC, Work Sheet and related documentation when needed.\nInitiating and owning quality records, including but not limited to non-conformances (NC), Corrective/Preventative (CAPA).\nProvides input to process improvements and assists with the development of new and/or improved manufacturing procedures.\nAssists with related special projects, as required.\n\nQualifications\n\n•Bachelor's degree (B.S.) in a scientific discipline (chemistry, molecular biology, biochemistry or related field) from four-year college or university with 0-3 years of experience including relevant industry experience in an FDA regulated company preferably in manufacturing and/or quality control.\n\n•General computer skills utilizing various software applications.\n\n•Experience in NAV\n\nPreferred\n\n•Experience with Mass Spectrometer and/or spectrophotometer plate reader.\n\n•Proven knowledge of cGMP requirements to ensure compliance.","company":"Elitechgroup","rawCompany":"elitechgroup","city":"Bothell","state":"WA","isRemote":false,"isActive":true,"createdAt":"2026-08-29T11:18:24.419Z","occupations":[{"code":"19-4031.00","title":"Chemical Technicians","slug":"chemical-technicians"},{"code":"19-4021.00","title":"Biological Technicians","slug":"biological-technicians"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325413","title":"In-Vitro Diagnostic Substance Manufacturing","slug":"in-vitro-diagnostic-substance-manufacturing"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Formulation Manufacturing Associate","description":"Summary\n\nFormulates oligonucleotide probes, primers and assays (RUO, ASR, EUA & 510K). Manages oligo stocks inventory. Assists Manager in managing RUO, ASR, EUA and 510K products inventory.\n\nEssential Duties and Responsibilities\n\nDissolves and dilutes oligonucleotide synthesis products, analyzes concentration, formulates assays (RUO, ASR, EUA & 510K), prints labels according to specifications and apply labels to product tubes.\nFormulate solutions mixes according to SOPs and Work Sheets (WS) to prepare finished products.\nPrepare and submit oligo samples for Mass Spec analysis.\nManages oligo stocks inventory.\nAssists Director/Manager in managing RUO, ASR, EUA and 510K products inventory.\nManufactures stocks of raw materials and buffers, and maintains lab supplies, etc.\nCalibrates and maintains lab equipment as required.\nMakes inventory corrections and consumptions in NAV.\nWriting manufacturing operating procedures that are technically sound, promote effective and efficient operations, and comply with cGMP requirements. Edit SOP, SEPC, Work Sheet and related documentation when needed.\nInitiating and owning quality records, including but not limited to non-conformances (NC), Corrective/Preventative (CAPA).\nProvides input to process improvements and assists with the development of new and/or improved manufacturing procedures.\nAssists with related special projects, as required.\n\nQualifications\n\n•Bachelor's degree (B.S.) in a scientific discipline (chemistry, molecular biology, biochemistry or related field) from four-year college or university with 0-3 years of experience including relevant industry experience in an FDA regulated company preferably in manufacturing and/or quality control.\n\n•General computer skills utilizing various software applications.\n\n•Experience in NAV\n\nPreferred\n\n•Experience with Mass Spectrometer and/or spectrophotometer plate reader.\n\n•Proven knowledge of cGMP requirements to ensure compliance.","datePosted":"2026-08-29T11:18:24.419Z","dateModified":"2026-08-29T11:18:24.419Z","hiringOrganization":{"@type":"Organization","name":"Elitechgroup","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Bothell","addressRegion":"WA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"726b7bb1c105587360ed6053"},"url":"https://jobsearcher.com/jobs/726b7bb1c105587360ed6053"}}