{"schemaVersion":"jobsearcher.job.v1","id":"be6624507b585e02ca60a07b","url":"https://jobsearcher.com/jobs/be6624507b585e02ca60a07b","canonicalUrl":"https://jobsearcher.com/jobs/be6624507b585e02ca60a07b","title":"Analytical Scientist","description":"About the RoleTechnical Source is seeking an Analytical Scientist to join a growing biotechnology organization developing next-generation genetic medicines. This role will support analytical testing activities for product characterization, release, and stability programs within a fast-paced and highly collaborative environment. The ideal candidate will have hands-on experience with molecular, cell-based, and/or biochemical assays in a regulated biopharmaceutical setting and a strong understanding of GMP documentation practices.ResponsibilitiesPerform routine analytical testing to support product characterization, release, and stability studiesExecute molecular, biochemical, and cell-based assays including techniques such as ELISA, PCR/ddPCR, Western blot, HPLC, capillary electrophoresis, and potency assaysFollow approved SOPs, protocols, and test methods while maintaining compliance with GMP documentation and data integrity requirementsReview and verify analytical data for accuracy, completeness, and complianceSupport method qualification, validation, transfer, and troubleshooting activitiesMaintain laboratory readiness through equipment calibration, preventative maintenance, reagent preparation, and inventory managementCollaborate with Manufacturing, Quality, Process Development, and Regulatory teams to support program objectivesAssist with internal audits, regulatory inspections, and data requestsContribute to SOP revisions, technical reports, and continuous improvement initiativesTrain and mentor junior laboratory personnel as neededRequired QualificationsBachelor's or Master's degree in Molecular Biology, Cell Biology, Biochemistry, Biotechnology, Pharmaceutical Sciences, or a related scientific discipline3+ years of experience in Analytical Sciences, Quality Control, Process Development, or related laboratory environments within biotechnology, pharmaceuticals, or gene therapyHands-on experience with at least one of the following: Cell-based potency assays, Molecular assays (PCR, qPCR, ddPCR, sequencing-based methods), Biochemical/protein assays (ELISA, Western blot, HPLC, capillary electrophoresis)Experience working within GMP-regulated environmentsFamiliarity with data integrity principles and regulatory expectationsStrong attention to detail and ability to execute protocol-driven laboratory workExcellent written and verbal communication skillsPreferred QualificationsExperience supporting biologics, viral vectors, gene therapy, vaccines, or cell therapy programsExperience with assay qualification, validation, or technology transfer activitiesFamiliarity with LIMS, electronic laboratory notebooks, or quality management systemsExperience supporting regulatory inspections and audit readinessKnowledge of ICH, USP, FDA, and GMP guidelinesPreferred BackgroundsGene therapy or viral vector analyticsBiologics or vaccine developmentQuality Control analytical testingMolecular biology and genomics laboratoriesBiopharmaceutical analytical development","company":"Technical Source","rawCompany":"technical source","city":"Boynton Beach","state":"FL","isRemote":false,"isActive":false,"createdAt":"2026-06-26T13:22:49.684Z","occupations":[{"code":"19-4021.00","title":"Biological Technicians","slug":"biological-technicians"},{"code":"19-1029.02","title":"Molecular and Cellular Biologists","slug":"molecular-and-cellular-biologists"},{"code":"19-1029.00","title":"Biological Scientists, All Other","slug":"biological-scientists-all-other"}],"industries":[{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"621511","title":"Medical Laboratories","slug":"medical-laboratories"},{"code":"325413","title":"In-Vitro Diagnostic Substance Manufacturing","slug":"in-vitro-diagnostic-substance-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Analytical Scientist","description":"About the RoleTechnical Source is seeking an Analytical Scientist to join a growing biotechnology organization developing next-generation genetic medicines. This role will support analytical testing activities for product characterization, release, and stability programs within a fast-paced and highly collaborative environment. The ideal candidate will have hands-on experience with molecular, cell-based, and/or biochemical assays in a regulated biopharmaceutical setting and a strong understanding of GMP documentation practices.ResponsibilitiesPerform routine analytical testing to support product characterization, release, and stability studiesExecute molecular, biochemical, and cell-based assays including techniques such as ELISA, PCR/ddPCR, Western blot, HPLC, capillary electrophoresis, and potency assaysFollow approved SOPs, protocols, and test methods while maintaining compliance with GMP documentation and data integrity requirementsReview and verify analytical data for accuracy, completeness, and complianceSupport method qualification, validation, transfer, and troubleshooting activitiesMaintain laboratory readiness through equipment calibration, preventative maintenance, reagent preparation, and inventory managementCollaborate with Manufacturing, Quality, Process Development, and Regulatory teams to support program objectivesAssist with internal audits, regulatory inspections, and data requestsContribute to SOP revisions, technical reports, and continuous improvement initiativesTrain and mentor junior laboratory personnel as neededRequired QualificationsBachelor's or Master's degree in Molecular Biology, Cell Biology, Biochemistry, Biotechnology, Pharmaceutical Sciences, or a related scientific discipline3+ years of experience in Analytical Sciences, Quality Control, Process Development, or related laboratory environments within biotechnology, pharmaceuticals, or gene therapyHands-on experience with at least one of the following: Cell-based potency assays, Molecular assays (PCR, qPCR, ddPCR, sequencing-based methods), Biochemical/protein assays (ELISA, Western blot, HPLC, capillary electrophoresis)Experience working within GMP-regulated environmentsFamiliarity with data integrity principles and regulatory expectationsStrong attention to detail and ability to execute protocol-driven laboratory workExcellent written and verbal communication skillsPreferred QualificationsExperience supporting biologics, viral vectors, gene therapy, vaccines, or cell therapy programsExperience with assay qualification, validation, or technology transfer activitiesFamiliarity with LIMS, electronic laboratory notebooks, or quality management systemsExperience supporting regulatory inspections and audit readinessKnowledge of ICH, USP, FDA, and GMP guidelinesPreferred BackgroundsGene therapy or viral vector analyticsBiologics or vaccine developmentQuality Control analytical testingMolecular biology and genomics laboratoriesBiopharmaceutical analytical development","datePosted":"2026-06-26T13:22:49.684Z","dateModified":"2026-06-26T13:22:49.684Z","hiringOrganization":{"@type":"Organization","name":"Technical Source","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Boynton Beach","addressRegion":"FL","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"be6624507b585e02ca60a07b"},"url":"https://jobsearcher.com/jobs/be6624507b585e02ca60a07b"}}