{"version":"0.1","company":{"name":"YubHub","url":"https://yubhub.co","jobsUrl":"https://yubhub.co/jobs/skill/elisa"},"x-facet":{"type":"skill","slug":"elisa","display":"Elisa","count":2},"x-feed-size-limit":100,"x-feed-sort":"enriched_at desc","x-feed-notice":"This feed contains at most 100 jobs (the most recently enriched). For the full corpus, use the paginated /stats/by-facet endpoint or /search.","x-generator":"yubhub-xml-generator","x-rights":"Free to redistribute with attribution: \"Data by YubHub (https://yubhub.co)\"","x-schema":"Each entry in `jobs` follows https://schema.org/JobPosting. YubHub-native raw fields carry `x-` prefix.","jobs":[{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_d5954a0d-cd7"},"title":"Associate Director, Analytical Development & QC","description":"<p><strong>Job Title</strong></p>\n<p>Associate Director, Analytical Development &amp; QC</p>\n<p><strong>About the Position</strong></p>\n<p>We are seeking a highly motivated, self-driven and detail-oriented Associate Director of Analytical Development and Quality Control to join our CMC team.</p>\n<p>This role will provide broad exposure across Formation Bio&#39;s portfolio, requiring the ability to flex between small molecule and biologics programs at different phases of development in an outsourced development model, requiring strong technical skillset, vendor management, and the ability to balance scientific rigor with program timelines.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>In close collaboration with CDMOs and contract testing laboratories, lead development, optimisation and validation of phase-appropriate analytical methods for small molecule and biologics drug substances and drug products.</li>\n<li>Manage testing (in-process, release, stability) at CDMOs and contract testing laboratories.</li>\n<li>Provide technical oversight for method transfers, comparability assessments, and laboratory readiness.</li>\n<li>Lead selection, qualification, and ongoing performance management of external analytical vendors.</li>\n<li>Oversee and manage Formation Bio&#39;s stability studies across all programs, including review and approval of stability protocols and review and trending of stability data to support shelf-life and retest dating. Track and publish stability program metrics. Act as the primary contact for stability-related inquiries.</li>\n<li>Oversee and manage Formation Bio&#39;s critical reagents and reference standards inventory and testing.</li>\n<li>Lead investigations of release and stability OOS and OOT results, deviations, CAPAs and change controls.</li>\n<li>Author and review analytical sections of CMC documents, including protocols, reports, and regulatory submissions.</li>\n<li>Author and review of SOPs and work instructions.</li>\n<li>Closely collaborate with CMC, QA, and Regulatory teams.</li>\n</ul>\n<p><strong>About You</strong></p>\n<ul>\n<li>Analytical Chemistry, Biochemistry, Molecular Biology, or a related discipline Master&#39;s degree with 5+ years or Bachelor&#39;s Degree with 8+ years of relevant small molecule and biologics analytical development and QC experience.</li>\n<li>Proven ability to operate effectively in a fast-paced, virtual, and outsourced development environment.</li>\n<li>Highly organised with a track record of managing multiple priorities across programs in an outsourced development model.</li>\n<li>Strong scientific judgement with the ability to independently assess data quality, identify risks, and recommend mitigation strategies.</li>\n<li>Ability to communicate complex analytical concepts clearly to both technical and non-technical stakeholders.</li>\n<li>Collaborative mindset with a strong sense of ownership and accountability.</li>\n<li>Extensive hands-on experience developing, optimising, and validating analytical methods for release and stability testing of small molecules and biologics.</li>\n<li>Hands-on experience with analytical methods pertinent to bilogics (qPCR, IEF, UHPLC, MS, CE, SDS-PAGE, ELISA, peptide mapping, glycan analysis, etc.) and small molecules (UHPLC, IC, GC, IR, UV, KF, PSD, dissolution, etc.).</li>\n<li>Experience with authoring and reviewing technical documents such as test methods, method development reports, validation protocols, validation reports, specification justification reports, retest and shelf-life memos, and SOPs.</li>\n<li>Experience with designing stability studies and performing stability data trending according to applicable guidances.</li>\n<li>Strong working knowledge of Smartsheet and JMP.</li>\n<li>Thorough understanding of ICH, FDA, EMA guidances and GMP requirements governing process development, manufacturing, and stability.</li>\n<li>Ability to travel domestically and internationally up to 25% of the time.</li>\n</ul>\n<p><strong>Total Compensation Range</strong></p>\n<p>$177,000 - $235,000</p>\n<p><strong>Where We Hire</strong></p>\n<p>Formation Bio is prioritising hiring in key hubs, primarily the New York City and Boston metro areas, with a hybrid model requiring 3 days per week in office. Applicants from the Research Triangle (NC) and San Francisco Bay Area may also be considered. Please apply only if you reside in these locations or are willing to relocate.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_d5954a0d-cd7","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Formation Bio","sameAs":"https://www.formationbio.com/","logo":"https://logos.yubhub.co/formationbio.com.png"},"x-apply-url":"https://job-boards.greenhouse.io/formationbio/jobs/7529162","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$177,000 - $235,000","x-skills-required":["Analytical Chemistry","Biochemistry","Molecular Biology","Small Molecule Analysis","Biologics Analysis","Method Development","Method Validation","Stability Testing","Quality Control","Regulatory Compliance","ICH Guidelines","FDA Guidelines","EMA Guidelines","GMP Requirements"],"x-skills-preferred":["Smartsheet","JMP","qPCR","IEF","UHPLC","MS","CE","SDS-PAGE","ELISA","Peptide Mapping","Glycan Analysis"],"datePosted":"2026-04-18T15:54:49.357Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"New York, NY; Boston, MA"}},"employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Technology","skills":"Analytical Chemistry, Biochemistry, Molecular Biology, Small Molecule Analysis, Biologics Analysis, Method Development, Method Validation, Stability Testing, Quality Control, Regulatory Compliance, ICH Guidelines, FDA Guidelines, EMA Guidelines, GMP Requirements, Smartsheet, JMP, qPCR, IEF, UHPLC, MS, CE, SDS-PAGE, ELISA, Peptide Mapping, Glycan Analysis","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":177000,"maxValue":235000,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_1d9019c9-d79"},"title":"Research Associate II","description":"<p>As a Research Associate II on Freenome&#39;s Scientific Operations team, you will be responsible for all things related to biospecimen accessioning as well as processing of whole blood samples into plasma, while also supporting downstream analytical testing using Freenome&#39;s multiomics assays.</p>\n<p>The role reports to Manager, Scientific Operations. This role will be an onsite role based in our Brisbane, California headquarters.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Perform routine lab work including pre-analytical sample processing, plasma isolation, and downstream genomics and proteomics assay processing.</li>\n<li>Operate liquid handler instruments to carry out experiments.</li>\n<li>Troubleshoot instrument and sample processing errors as needed; escalate and report issues through appropriate channels as needed.</li>\n<li>Identify and implement process improvements across the lab by thinking critically about the execution of all experiments.</li>\n<li>Verify all aspects of incoming specimens and assess acceptability for analytical testing.</li>\n<li>Maintain documentation for executed experiments.</li>\n<li>Perform equipment maintenance according to the laboratory&#39;s standard operating procedures for the following but not limited to: Hamiltons, Biosafety Cabinets, centrifuges, freezers, refrigerators, and pipettes, as needed.</li>\n<li>Assist with training of new laboratory personnel and training of new procedures with existing personnel.</li>\n<li>Document all corrective actions taken when test systems deviate from the laboratory&#39;s established performance specifications.</li>\n<li>Report all concerns of test quality and/or safety to the Supervisor or Safety Officer.</li>\n<li>Perform other miscellaneous laboratory duties as assigned and assist others as time allows.</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>Bachelor&#39;s degree or Master&#39;s degree in molecular biology, biochemistry, genetics, chemical biology, or a related field.</li>\n<li>2+ years relevant industry experience in a laboratory setting.</li>\n<li>Experience working with 96 or 384 well plate format assays.</li>\n<li>Proven track record of following SOPs, work instructions or experimental designs to completion.</li>\n<li>Strong organizational skills and attention to detail.</li>\n<li>Ability to work, execute, and troubleshoot protocols independently.</li>\n</ul>\n<p>Nice to Have:</p>\n<ul>\n<li>Working understanding of GLP.</li>\n<li>Experience with NGS library preparation and/or sequencing.</li>\n<li>Experience with ELISA, Luminex, or other immunoassays.</li>\n<li>Familiarity with Liquid Handlers - Bravo, Hamilton, etc.</li>\n</ul>\n<p>Benefits and Additional Information:</p>\n<p>The US target range of our hourly rate for new hires is $37.68 - $46.69. You will also be eligible to receive equity, cash bonuses, and a full range of medical, financial, and other benefits depending on the position offered. Please note that individual total compensation for this position will be determined at the Company&#39;s sole discretion and may vary based on several factors, including but not limited to, location, skill level, years and depth of relevant experience, and education.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_1d9019c9-d79","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Freenome","sameAs":"https://freenome.com","logo":"https://logos.yubhub.co/freenome.com.png"},"x-apply-url":"https://job-boards.greenhouse.io/freenome/jobs/8433576002","x-work-arrangement":"onsite","x-experience-level":"mid","x-job-type":"full-time","x-salary-range":"$37.68 - $46.69 per hour","x-skills-required":["Molecular biology","Biochemistry","Genetics","Chemical biology","Laboratory management","Sample processing","Genomics","Proteomics","Liquid handler instruments","Troubleshooting","Process improvement","Equipment maintenance"],"x-skills-preferred":["GLP","NGS library preparation","Sequencing","ELISA","Luminex","Immunoassays","Liquid handlers"],"datePosted":"2026-04-17T12:36:03.086Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Brisbane, California"}},"employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Technology","skills":"Molecular biology, Biochemistry, Genetics, Chemical biology, Laboratory management, Sample processing, Genomics, Proteomics, Liquid handler instruments, Troubleshooting, Process improvement, Equipment maintenance, GLP, NGS library preparation, Sequencing, ELISA, Luminex, Immunoassays, Liquid handlers"}]}