Analytical Chemist (Contractor)

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    "description": "<p style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><b><span lang=\"EN\" style=\"font-family:&quot;Calibri&quot;,sans-serif\">About Us</span></b></span></span></span></p>\r\n\r\n<p style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"background:white\"><span style=\"vertical-align:baseline\"><span style=\"line-height:115%\"><span style=\"font-family:Arial,sans-serif\"><b><span lang=\"EN\" style=\"font-family:&quot;Calibri&quot;,sans-serif\"><span style=\"color:black\">Fulgent Pharma LLC, a Fulgent Genetics Company</span></span></b><span lang=\"EN\" style=\"font-family:&quot;Calibri&quot;,sans-serif\"><span style=\"color:black\">, is focused on developing and commercializing innovative anti-cancer therapies that shift the field of cancer treatment toward more effective and more personalized medicine.&nbsp;</span></span></span></span></span></span></span></p>\r\n\r\n<p style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"background:white\"><span style=\"vertical-align:baseline\"><span style=\"line-height:115%\"><span style=\"font-family:Arial,sans-serif\"><span lang=\"EN\" style=\"font-family:&quot;Calibri&quot;,sans-serif\"><span style=\"color:black\">Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service genomic testing company built around a foundational technology platform.</span></span></span></span></span></span></span></p>\r\n\r\n<p style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"background:white\"><span style=\"vertical-align:baseline\"><span style=\"line-height:115%\"><span style=\"font-family:Arial,sans-serif\"><span lang=\"EN\" style=\"font-family:&quot;Calibri&quot;,sans-serif\"><span style=\"color:black\">Through our diverse testing menu, Fulgent is focused on transforming patient care in oncology, anatomic pathology, infectious and rare diseases, and reproductive health. We believe that by providing a wide range of effective, flexible testing options in conjunction with best-in-class service and support, we can redefine the way medicine is managed for patients and clinicians alike.</span></span></span></span></span></span></span></p>\r\n\r\n<p style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"background:white\"><span style=\"vertical-align:baseline\"><span style=\"line-height:115%\"><span style=\"font-family:Arial,sans-serif\"><span lang=\"EN\" style=\"font-family:&quot;Calibri&quot;,sans-serif\"><span style=\"color:black\">As Fulgent&#39;s therapeutic development business, Fulgent Pharma LLC, is developing drug candidates for treating a broad range of cancers using a novel nanoencapsulation and targeted therapy platform. By merging Fulgent Genetics and Fulgent Pharma&#39;s fields of expertise, we aim to become a fully integrated precision medicine company.</span></span></span></span></span></span></span></p>\r\n\r\n<p style=\"text-align:justify\">&nbsp;</p>\r\n\r\n<p style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><b><span lang=\"EN\" style=\"font-family:&quot;Calibri&quot;,sans-serif\">Summary of Position</span></b></span></span></span></p>\r\n\r\n<p style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span lang=\"EN\" style=\"font-family:&quot;Calibri&quot;,sans-serif\">The Analytical Chemist (Contractor)<b> </b>is to assist the Analytical Director to lead/coordinate the technical and scientific efforts for physical and chemical characterizations using HPLC, GC, SEC, LS, PM, method development, validation, implementation, testing, reporting and method transfer to support pharmaceutical R&amp;D, CMC, and support regulatory filing for drug compounds and formulations.</span></span></span></span></p>\r\n\r\n<p style=\"text-align:justify\">&nbsp;</p>\r\n\r\n<p style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><b><span lang=\"EN\" style=\"font-family:&quot;Calibri&quot;,sans-serif\">Key Job Elements</span></b></span></span></span></p>\r\n\r\n<ul>\r\n\t<li style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Independently develops, optimizes, qualifies, validates, troubleshoots, and transfers HPLC/UPLC methods for assay, potency/content, related substances, degradation products, residual free drug, process impurities, formulation components, and stability-indicating applications.</span></span></span></span></li>\r\n\t<li style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Executes phase-appropriate analytical method validation activities, including specificity, accuracy, precision, linearity, range, LOD/LOQ, robustness, system suitability, forced degradation, solution stability, and sample stability assessments.</span></span></span></span></li>\r\n\t<li style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Performs CMC analytical testing for APIs, polymers/excipients, linkers/payloads where applicable, formulated drug products, and development batches, including release, in-process, characterization, and stability testing.</span></span></span></span></li>\r\n\t<li style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Performs or supports additional CMC and physical-chemical testing, which may include GC/residual solvents, SEC, UV/Vis, FTIR, light scattering/particle size, particulate matter/subvisible particles, pH, osmolality, viscosity, appearance, water content, concentration, and formulation performance testing.</span></span></span></span></li>\r\n\t<li style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Prepares and reviews analytical protocols, worksheets, raw data packages, method development reports, validation reports, R&amp;D reports, stability summaries, investigation reports, and analytical source documents for CMC sections of IND/NDA or other regulatory submissions.</span></span></span></span></li>\r\n\t<li style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Maintains, calibrates, and troubleshoots analytical instruments, especially HPLC/UPLC systems and chromatography data systems; ensures instrument logbooks, preventive maintenance, calibration, reference standards, reagents, columns, and consumables are properly controlled.</span></span></span></span></li>\r\n\t<li style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Supports stability programs by coordinating sample pulls, executing testing, trending stability data, evaluating OOT/OOS results, and communicating potential product quality risks in a timely manner.</span></span></span></span></li>\r\n\t<li style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Supports CRO/CMO/CDMO analytical activities, including method transfer, technical oversight, protocol/report review, data review, deviation investigation, and communication of analytical requirements for manufacturing and release testing.</span></span></span></span></li>\r\n\t<li style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Participates in laboratory investigations, OOS/OOT/deviation assessments, CAPA, change control, data integrity review, and continuous improvement of analytical procedures and laboratory systems.</span></span></span></span></li>\r\n\t<li style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Works closely with R&amp;D, manufacturing, quality, regulatory, and operations teams to improve workflow efficiency, documentation quality, testing readiness, and CMC package completeness.</span></span></span></span></li>\r\n\t<li style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Adheres to safety and security standards, company policies, applicable SOPs, and laboratory good documentation practices.</span></span></span></span></li>\r\n\t<li style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Completes Daily Timesheet accurately and submits as required.</span></span></span></span></li>\r\n\t<li style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Performs other duties as assigned, such as assay development, sample management, reference standard coordination, vendor/CRO communication, and drafting technical responses to internal or regulatory questions.</span></span></span></span></li>\r\n</ul>\r\n",
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The position may provide technical guidance, training, and day-to-day coordination to junior scientists, analysts, interns, or technicians as assigned.\\r\\n\\r\\n\\r\\nReports To:\\r\\n\\r\\n\\r\\n\\tDirector of Bioanalytical Sciences\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nEnvironment\\r\\n\\r\\nFulgent Therapeutics LLC is an Equal Employment Opportunity Employer.\\r\\n\\r\\nThe work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. 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By merging Fulgent Genetics and Fulgent Pharma&#39;s fields of expertise, we aim to become a fully integrated precision medicine company.\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nSummary of Position\\r\\n\\r\\nThe Analytical Chemist (Contractor) is to assist the Analytical Director to lead/coordinate the technical and scientific efforts for physical and chemical characterizations using HPLC, GC, SEC, LS, PM, method development, validation, implementation, testing, reporting and method transfer to support pharmaceutical R&amp;D, CMC, and support regulatory filing for drug compounds and formulations.\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nKey Job Elements\\r\\n\\r\\n\\r\\n\\tIndependently develops, optimizes, qualifies, validates, troubleshoots, and transfers HPLC/UPLC methods for assay, potency/content, related substances, degradation products, residual free drug, process impurities, formulation components, and stability-indicating applications.\\r\\n\\tExecutes phase-appropriate analytical method validation activities, including specificity, accuracy, precision, linearity, range, LOD/LOQ, robustness, system suitability, forced degradation, solution stability, and sample stability assessments.\\r\\n\\tPerforms CMC analytical testing for APIs, polymers/excipients, linkers/payloads where applicable, formulated drug products, and development batches, including release, in-process, characterization, and stability testing.\\r\\n\\tPerforms or supports additional CMC and physical-chemical testing, which may include GC/residual solvents, SEC, UV/Vis, FTIR, light scattering/particle size, particulate matter/subvisible particles, pH, osmolality, viscosity, appearance, water content, concentration, and formulation performance testing.\\r\\n\\tPrepares and reviews analytical protocols, worksheets, raw data packages, method development reports, validation reports, R&amp;D reports, stability summaries, investigation reports, and analytical source documents for CMC sections of IND/NDA or other regulatory submissions.\\r\\n\\tMaintains, calibrates, and troubleshoots analytical instruments, especially HPLC/UPLC systems and chromatography data systems; ensures instrument logbooks, preventive maintenance, calibration, reference standards, reagents, columns, and consumables are properly controlled.\\r\\n\\tSupports stability programs by coordinating sample pulls, executing testing, trending stability data, evaluating OOT/OOS results, and communicating potential product quality risks in a timely manner.\\r\\n\\tSupports CRO/CMO/CDMO analytical activities, including method transfer, technical oversight, protocol/report review, data review, deviation investigation, and communication of analytical requirements for manufacturing and release testing.\\r\\n\\tParticipates in laboratory investigations, OOS/OOT/deviation assessments, CAPA, change control, data integrity review, and continuous improvement of analytical procedures and laboratory systems.\\r\\n\\tWorks closely with R&amp;D, manufacturing, quality, regulatory, and operations teams to improve workflow efficiency, documentation quality, testing readiness, and CMC package completeness.\\r\\n\\tAdheres to safety and security standards, company policies, applicable SOPs, and laboratory good documentation practices.\\r\\n\\tCompletes Daily Timesheet accurately and submits as required.\\r\\n\\tPerforms other duties as assigned, such as assay development, sample management, reference standard coordination, vendor/CRO communication, and drafting technical responses to internal or regulatory questions.\\r\\n\\r\\n\",\"employmentType\":\"CONTRACTOR\",\"hiringOrganization\":{\"@type\":\"Organization\",\"name\":\"FULGENT THERAPEUTICS LLC\",\"logo\":\"https://www.paycomonline.net/v4/ats/web.php/application/style/logo?clientkey=E86D60EDAF14F62BD0B3F719F912C645\"},\"jobLocation\":{\"@type\":\"Place\",\"address\":{\"streetAddress\":\"824 Interchange Blvd\",\"addressLocality\":\"Newark\",\"addressRegion\":\"DE\",\"postalCode\":19711,\"addressCountry\":\"USA\"}},\"qualifications\":\"Knowledge/Experience\\r\\n\\r\\n\\r\\n\\tBachelor of Science degree with minimum 6 years of laboratory experience or Master&rsquo;s Degree with 4 years of laboratory experience or Ph.D. with 2 years of postgraduate research in Chemistry, Biology or related science disciplines\\r\\n\\tStrong hands-on experience with HPLC/UPLC method development, troubleshooting, validation, and routine drug analysis is required.\\r\\n\\tExperience independently executing method validation studies and preparing validation protocols/reports for pharmaceutical drug development is strongly preferred.\\r\\n\\tExperience with CMC analytical testing for APIs, formulated drug products, impurities/degradants, stability samples, and/or polymer- or nanoparticle-based formulations is preferred.\\r\\n\\tFamiliarity with cGMP/GLP expectations, good documentation practices, data integrity principles, ICH analytical validation guidance, FDA CMC expectations, and phase-appropriate analytical development practices.\\r\\n\\tExperience with instrument maintenance, calibration, and troubleshooting for HPLC/UPLC and other analytical equipment.\\r\\n\\tExperience working with CROs/CMOs/CDMOs, method transfer, external data review, and technical communication is preferred.\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nAdditional Skills\\r\\n\\r\\n\\r\\n\\tStrong practical knowledge of analytical chemistry, organic chemistry, pharmaceutical analysis, and chromatographic separation principles.\\r\\n\\tAbility to independently design experiments, troubleshoot analytical methods, interpret complex chromatograms/data, and recommend scientifically justified next steps.\\r\\n\\tAbility to work in a fast-paced small-company environment and prioritize multiple development, stability, and CMC documentation activities.\\r\\n\\tAbility to maintain confidentiality, meet deadlines, and follow company SOPs, safety practices, and documentation expectations.\\r\\n\\tPreferred experience with oncology drug products, poorly soluble drug formulations, polymer excipients, nanoparticles, ADC-related analytical methods, or a combination of small-molecule and biologics/bioconjugate testing.\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nSupervisory Responsibilities:\\r\\n\\r\\n\\r\\n\\tNo direct reports are required for this role. The position may provide technical guidance, training, and day-to-day coordination to junior scientists, analysts, interns, or technicians as assigned.\\r\\n\\r\\n\\r\\nReports To:\\r\\n\\r\\n\\r\\n\\tDirector of Bioanalytical Sciences\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nEnvironment\\r\\n\\r\\nFulgent Therapeutics LLC is an Equal Employment Opportunity Employer.\\r\\n\\r\\nThe work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. The term &ldquo;qualified individual with a disability&rdquo; means an individual with a disability who, with or without reasonable accommodation, can perform the essential functions of the position.\\r\\n\",\"experienceRequirements\":\"Knowledge/Experience\\r\\n\\r\\n\\r\\n\\tBachelor of Science degree with minimum 6 years of laboratory experience or Master&rsquo;s Degree with 4 years of laboratory experience or Ph.D. with 2 years of postgraduate research in Chemistry, Biology or related science disciplines\\r\\n\\tStrong hands-on experience with HPLC/UPLC method development, troubleshooting, validation, and routine drug analysis is required.\\r\\n\\tExperience independently executing method validation studies and preparing validation protocols/reports for pharmaceutical drug development is strongly preferred.\\r\\n\\tExperience with CMC analytical testing for APIs, formulated drug products, impurities/degradants, stability samples, and/or polymer- or nanoparticle-based formulations is preferred.\\r\\n\\tFamiliarity with cGMP/GLP expectations, good documentation practices, data integrity principles, ICH analytical validation guidance, FDA CMC expectations, and phase-appropriate analytical development practices.\\r\\n\\tExperience with instrument maintenance, calibration, and troubleshooting for HPLC/UPLC and other analytical equipment.\\r\\n\\tExperience working with CROs/CMOs/CDMOs, method transfer, external data review, and technical communication is preferred.\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nAdditional Skills\\r\\n\\r\\n\\r\\n\\tStrong practical knowledge of analytical chemistry, organic chemistry, pharmaceutical analysis, and chromatographic separation principles.\\r\\n\\tAbility to independently design experiments, troubleshoot analytical methods, interpret complex chromatograms/data, and recommend scientifically justified next steps.\\r\\n\\tAbility to work in a fast-paced small-company environment and prioritize multiple development, stability, and CMC documentation activities.\\r\\n\\tAbility to maintain confidentiality, meet deadlines, and follow company SOPs, safety practices, and documentation expectations.\\r\\n\\tPreferred experience with oncology drug products, poorly soluble drug formulations, polymer excipients, nanoparticles, ADC-related analytical methods, or a combination of small-molecule and biologics/bioconjugate testing.\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nSupervisory Responsibilities:\\r\\n\\r\\n\\r\\n\\tNo direct reports are required for this role. The position may provide technical guidance, training, and day-to-day coordination to junior scientists, analysts, interns, or technicians as assigned.\\r\\n\\r\\n\\r\\nReports To:\\r\\n\\r\\n\\r\\n\\tDirector of Bioanalytical Sciences\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nEnvironment\\r\\n\\r\\nFulgent Therapeutics LLC is an Equal Employment Opportunity Employer.\\r\\n\\r\\nThe work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. The term &ldquo;qualified individual with a disability&rdquo; means an individual with a disability who, with or without reasonable accommodation, can perform the essential functions of the position.\\r\\n\",\"industry\":\"Biotech\",\"validThrough\":\"-0001-11-30\",\"educationRequirements\":\"4 Year Degree\"}",
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    "qualifications": "<p style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><b><span lang=\"EN\" style=\"font-family:&quot;Calibri&quot;,sans-serif\">Knowledge/Experience</span></b></span></span></span></p>\r\n\r\n<ul>\r\n\t<li style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Bachelor of Science degree with minimum 6 years of laboratory experience or Master&rsquo;s Degree with 4 years of laboratory experience or Ph.D. with 2 years of postgraduate research in Chemistry, Biology or related science disciplines</span></span></span></span></li>\r\n\t<li style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Strong hands-on experience with HPLC/UPLC method development, troubleshooting, validation, and routine drug analysis is required.</span></span></span></span></li>\r\n\t<li style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Experience independently executing method validation studies and preparing validation protocols/reports for pharmaceutical drug development is strongly preferred.</span></span></span></span></li>\r\n\t<li style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Experience with CMC analytical testing for APIs, formulated drug products, impurities/degradants, stability samples, and/or polymer- or nanoparticle-based formulations is preferred.</span></span></span></span></li>\r\n\t<li style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Familiarity with cGMP/GLP expectations, good documentation practices, data integrity principles, ICH analytical validation guidance, FDA CMC expectations, and phase-appropriate analytical development practices.</span></span></span></span></li>\r\n\t<li style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Experience with instrument maintenance, calibration, and troubleshooting for HPLC/UPLC and other analytical equipment.</span></span></span></span></li>\r\n\t<li style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Experience working with CROs/CMOs/CDMOs, method transfer, external data review, and technical communication is preferred.</span></span></span></span></li>\r\n</ul>\r\n\r\n<p style=\"text-align:justify\">&nbsp;</p>\r\n\r\n<p style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><b><span lang=\"EN\" style=\"font-family:&quot;Calibri&quot;,sans-serif\">Additional Skills</span></b></span></span></span></p>\r\n\r\n<ul>\r\n\t<li style=\"margin-left:32px; text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Strong practical knowledge of analytical chemistry, organic chemistry, pharmaceutical analysis, and chromatographic separation principles.</span></span></span></span></li>\r\n\t<li style=\"margin-left:32px; text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Ability to independently design experiments, troubleshoot analytical methods, interpret complex chromatograms/data, and recommend scientifically justified next steps.</span></span></span></span></li>\r\n\t<li style=\"margin-left:32px; text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Ability to work in a fast-paced small-company environment and prioritize multiple development, stability, and CMC documentation activities.</span></span></span></span></li>\r\n\t<li style=\"margin-left:32px; text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Ability to maintain confidentiality, meet deadlines, and follow company SOPs, safety practices, and documentation expectations.</span></span></span></span></li>\r\n\t<li style=\"margin-left:32px; text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Preferred experience with oncology drug products, poorly soluble drug formulations, polymer excipients, nanoparticles, ADC-related analytical methods, or a combination of small-molecule and biologics/bioconjugate testing.</span></span></span></span></li>\r\n</ul>\r\n\r\n<p style=\"text-align:justify\">&nbsp;</p>\r\n\r\n<p style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><b><span lang=\"EN\" style=\"font-family:&quot;Calibri&quot;,sans-serif\">Supervisory Responsibilities:</span></b></span></span></span></p>\r\n\r\n<ul>\r\n\t<li style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">No direct reports are required for this role. The position may provide technical guidance, training, and day-to-day coordination to junior scientists, analysts, interns, or technicians as assigned.</span></span></span></span></li>\r\n</ul>\r\n\r\n<p style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><b><span lang=\"EN\" style=\"font-family:&quot;Calibri&quot;,sans-serif\">Reports To:</span></b></span></span></span></p>\r\n\r\n<ul>\r\n\t<li style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Director of Bioanalytical Sciences</span></span></span></span></li>\r\n</ul>\r\n\r\n<p style=\"text-align:justify\">&nbsp;</p>\r\n\r\n<p style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><b><span lang=\"EN\" style=\"font-family:&quot;Calibri&quot;,sans-serif\">Environment</span></b></span></span></span></p>\r\n\r\n<p style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">Fulgent Therapeutics LLC is an Equal Employment Opportunity Employer.</span></span></span></span></p>\r\n\r\n<p style=\"text-align:justify\"><span style=\"font-size:11pt\"><span style=\"line-height:normal\"><span style=\"font-family:Arial,sans-serif\"><span style=\"font-family:&quot;Calibri&quot;,sans-serif\">The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. The term &ldquo;qualified individual with a disability&rdquo; means an individual with a disability who, with or without reasonable accommodation, can perform the essential functions of the position.</span></span></span></span></p>\r\n",
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