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YubHub-native raw fields carry `x-` prefix.","jobs":[{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_e5385550-532"},"title":"Senior Scientist-Analytical Project Lead, Global Product Development","description":"<p>Are you ready to shape the future of medicines,pioneering technical and scientific breakthroughs that transform patient lives? We are seeking an experienced and innovative Analytical Project Lead based in Durham, North Carolina.</p>\n<p>Our vision is to transform product design, development, and characterization to enable delivery of new medicines to patients. In this role, you will lead analytical strategy and delivery for oral solid dosage (OSD) forms and, as needed, inhaled and/or parenteral products from early development through clinical supply and toward commercialization.</p>\n<p>As the analytical project/skill lead, you will partner across formulation, engineering, biopharmaceutics, manufacturing, QA and Regulatory to deliver robust methods, efficient control strategies, and submission-ready documentation. You will also help establish and optimize OSD laboratory capabilities at the Durham site, champion laboratory automation, and encourage adoption of modern data analytics and AI/ML tools to accelerate development and interpretation.</p>\n<p>We work, on average, a minimum of three days per week from the office. We balance the expectation of being in the office while respecting individual flexibility.</p>\n<p>Responsibilities include, but are not limited to:</p>\n<ul>\n<li>Project leadership: Act as analytical skill lead to secure major drug product deliveries, applying a risk-based, flexible approach to prioritization, resources, and timelines across modalities and dosage forms; integrate analytical plans with global teams and external partners/CMOs.</li>\n</ul>\n<ul>\n<li>Analytical strategy &amp; control: Define and own a phase-appropriate analytical control strategy aligned with CMC expectations across clinical phases; harmonize methods and embed lifecycle management to ensure robust, efficient control.</li>\n</ul>\n<ul>\n<li>Method development &amp; validation: Design, develop, validate, transfer, and lifecycle manage analytical methods for OSD (e.g., HPLC/UPLC, LC–MS, dissolution, impurity profiling, stability-indicating capability); establish scientifically supported system suitability, specifications, and fit-for-purpose sample preparation; ensure readiness for GMP execution with clear documentation and analyst guidance. Support inhaled and/or parenteral methods as needed.</li>\n</ul>\n<ul>\n<li>Characterization &amp; performance: Lead drug product characterization, comparability, and stability programs; direct forced degradation studies; for inhaled products where required, support aerodynamic performance assessments (e.g., impactor analysis).</li>\n</ul>\n<ul>\n<li>CMC &amp; regulatory: Author and review analytical CMC content for IND/IMPD/NDA/MAA; prepare validation reports, method transfer documents, and specifications; lead responses to regulatory queries and support shelf life assignment with appropriate statistics.</li>\n</ul>\n<ul>\n<li>Cross-functional collaboration: Work closely with formulators, engineers, supply and manufacturing sites, QA, Regulatory, and external partners/CMOs to integrate analytical deliverables into project plans and clinical manufacturing.</li>\n</ul>\n<ul>\n<li>Durham lab capability &amp; technology: Champion laboratory automation for sample preparation, method execution, and data analysis under GxP control.</li>\n</ul>\n<ul>\n<li>Problem-solving: Lead complex investigations, root cause analyses, and data integrity assessments; apply structured problem-solving (e.g., Six Sigma) and statistics to drive timely resolution and preventive actions.</li>\n</ul>\n<ul>\n<li>Digital, data &amp; innovation: Apply DoE and statistics for method robustness and understanding; use ELN/CDS and statistical tools; promote AI/ML, chemometrics, and predictive analytics to enhance interpretation, specification setting, and development speed; enable learning and standardization across projects; chip in to patenting and/or publishing.</li>\n</ul>\n<ul>\n<li>Quality &amp; governance: Ensure GxP compliance where applicable, data integrity, rigorous study design, and clear communication to governance bodies.</li>\n</ul>\n<p>Minimum Qualifications:</p>\n<ul>\n<li>Bachelor’s (12+ years), Master’s (6+ years), or PhD (or equivalent experience) in Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, Biotechnology, or related field.</li>\n</ul>\n<ul>\n<li>Significant experience in pharmaceutical analytical science with current knowledge of regulatory CMC requirements for clinical and/or marketing applications.</li>\n</ul>\n<ul>\n<li>Demonstrated experience in analytical development for oral solid dosage forms; additional experience with inhaled and/or parenteral products preferred.</li>\n</ul>\n<ul>\n<li>Consistent record leading teams and/or scientific projects within a global organization and with external partners/CMOs; ability to influence cross-functional strategies.</li>\n</ul>\n<ul>\n<li>Strong proficiency with chromatographic techniques (HPLC/UPLC; LC–MS), dissolution, and complementary methodologies; for inhaled products, familiarity with aerosol performance characterization is a plus.</li>\n</ul>\n<ul>\n<li>Hands-on experience in method development (including use of supporting software), validation, transfer, and lifecycle management under ICH guidelines and phase-appropriate frameworks.</li>\n</ul>\n<ul>\n<li>Experience authoring analytical CMC content for submissions and responding to regulatory queries across clinical development.</li>\n</ul>\n<ul>\n<li>Experience working in a GMP/GxP environment; familiarity with instrument/equipment qualification, calibration, and maintenance expectations.</li>\n</ul>\n<ul>\n<li>Excellent communication, customer management, and influencing skills; ability to operate confidently and collaboratively across global, cross-disciplinary environments.</li>\n</ul>\n<ul>\n<li>Demonstrated ability to troubleshoot technical challenges and drive data-driven decisions.</li>\n</ul>\n<ul>\n<li>Fundamental digital and data capability relevant to analytical development, including:</li>\n</ul>\n<ul>\n<li>Proficiency with multivariate experimental design and basic DoE concepts for method and process understanding</li>\n</ul>\n<ul>\n<li>Working knowledge of statistics for analytical science (e.g., regression, ANOVA, capability/variation analysis, stability trending, OOS/OOT investigation)</li>\n</ul>\n<ul>\n<li>Practical use of ELN/CDS and statistical software (e.g., JMP or Minitab) for data analysis and reporting</li>\n</ul>\n<p>Preferred Qualifications:</p>\n<ul>\n<li>Strategic chromatographic and separation science leadership: define orthogonal method suites (e.g., RP, HILIC, ion exchange, SEC, SFC, CE) to secure impurity resolution and stability-indicating capability; apply LC–MS(/MS) for structure confirmation and quantitation; use multidimensional LC and targeted DoE to accelerate development and set robust specifications; harmonize methods across sites with clear comparability criteria; embed lifecycle management and coach teams through complex separations (e.g., peptides, oligonucleotides, challenging matrices).</li>\n</ul>\n<ul>\n<li>OSD focus: Support with establishing, equipping, and optimizing OSD test equipment and processes at the Durham site.</li>\n</ul>\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_e5385550-532","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Analytical Development","sameAs":"https://astrazeneca.eightfold.ai","logo":"https://logos.yubhub.co/astrazeneca.eightfold.ai.png"},"x-apply-url":"https://astrazeneca.eightfold.ai/careers/job/563877689929250","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Analytical Chemistry","Pharmaceutical Sciences","Biochemistry","Biotechnology","Chromatographic techniques","Dissolution","LC–MS","HPLC/UPLC","Method development","Validation","Transfer","Lifecycle management","ICH guidelines","Phase-appropriate frameworks","Analytical CMC content","Regulatory queries","GMP/GxP environment","Instrument/equipment qualification","Calibration","Maintenance","Experimental design","Statistics","ELN/CDS","Statistical software","Data analysis","Reporting"],"x-skills-preferred":["Strategic chromatographic and separation science leadership","Orthogonal method suites","LC–MS(/MS)","Multidimensional LC","Targeted DoE","Robust specifications","Harmonized methods","Complex separations","Peptides","Oligonucleotides","Challenging matrices","OSD focus","Establishing","Equipping","Optimizing","Test equipment","Processes"],"datePosted":"2026-04-24T14:13:54.042Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Durham, North Carolina, United States of America"}},"employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Healthcare","skills":"Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, Biotechnology, Chromatographic techniques, Dissolution, LC–MS, HPLC/UPLC, Method development, Validation, Transfer, Lifecycle management, ICH guidelines, Phase-appropriate frameworks, Analytical CMC content, Regulatory queries, GMP/GxP environment, Instrument/equipment qualification, Calibration, Maintenance, Experimental design, Statistics, ELN/CDS, Statistical software, Data analysis, Reporting, Strategic chromatographic and separation science leadership, Orthogonal method suites, LC–MS(/MS), Multidimensional LC, Targeted DoE, Robust specifications, Harmonized methods, Complex separations, Peptides, Oligonucleotides, Challenging matrices, OSD focus, Establishing, Equipping, Optimizing, Test equipment, Processes"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_e701b46c-e93"},"title":"Analytical Chemistry Manager","description":"<p>At Bp, we are seeking an experienced Analytical Chemistry Manager to join our team. The successful candidate will be responsible for shaping and managing the analytical chemistry team, with a specific focus on modernizing workflows through automation.</p>\n<p>The role will oversee a team developing, validating, and implementing analytical methods, managing high-throughput instruments, and ensuring data integrity and compliance with regulatory standards. The manager will drive efficiency by leveraging automated systems and AI-driven data analysis, contributing to the Bp strategic framework across fuels (including biofuels), SAF, biogas, feedstocks, hydrogen, oil and gas, and cross-cutting low-carbon initiatives.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Delivery of safe and compliant experimental operations and support of an HSSE culture.</li>\n<li>Management of the portfolio in analytical chemistry, including lead development, optimisation, and validation of analytical methods (HPLC, GC, GC-MS, LC-MS, ICP, NMR, etc.).</li>\n<li>Design, build, and deployment of high-throughput analytical automation systems (e.g. automated LC-MS, robotics).</li>\n<li>Integration of analytical workflows with existing laboratory information management systems (LIMS) and electronic lab notebooks (ELN).</li>\n<li>Implementation of AI and advanced software to speed up method development, data interpretation, and chromatography optimisation.</li>\n<li>Development, management, and delivery of the Team&#39;s annual programme according to resources and priorities.</li>\n</ul>\n<p>The ideal candidate will have at least ten years&#39; professional experience in an analytical science environment, a PhD in Chemistry (or MSc/BSc with 15+ years of experience), and a strong grasp of underlying fundamentals of analytical chemistry.</p>\n<p>They will also have a record of strong scientific and team leadership, effective communication skills, and a proven track record of decision-making and appropriate risk-taking.</p>\n<p>The role requires strong networking and influencing skills, and the ability to manage delivery of multiple projects across multiple interfaces.</p>\n<p>Travel is expected to be up to 10%.</p>\n<p>We are an equal opportunities employer and welcome applications from diverse candidates.</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_e701b46c-e93","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Bp","sameAs":"https://careers.bp.com","logo":"https://logos.yubhub.co/careers.bp.com.png"},"x-apply-url":"https://careers.bp.com/job-description/RQ109815","x-work-arrangement":"onsite","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Analytical Chemistry","Method Development","Automation","AI-Driven Data Analysis","Regulatory Compliance","Leadership","Communication","Risk Management"],"x-skills-preferred":["Computational Chemistry","Lab Automation","Robotics","Electronic Lab Notebooks","Laboratory Information Management Systems"],"datePosted":"2026-04-24T12:14:15.410Z","employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Energy","skills":"Analytical Chemistry, Method Development, Automation, AI-Driven Data Analysis, Regulatory Compliance, Leadership, Communication, Risk Management, Computational Chemistry, Lab Automation, Robotics, Electronic Lab Notebooks, Laboratory Information Management Systems"},{"@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"}}}]}