{"schemaVersion":"jobsearcher.job.v1","id":"62ea836e2e751c308f2d7ff7","url":"https://jobsearcher.com/jobs/62ea836e2e751c308f2d7ff7","canonicalUrl":"https://jobsearcher.com/jobs/62ea836e2e751c308f2d7ff7","title":"QC Chemist Pharma Analytics & Method Validation","description":"Job Responsibilities:\nPerform routine chemical analyses using HPLC, GC, UV-Vis, FTIR, titration, and other analytical techniques.\nConduct stability testing and method validations according to ICH guidelines.\nPrepare and standardize laboratory reagents and solutions.\nAccurately document test results in accordance with cGMP requirements and Good Documentation Practices (GDP).\nReview and interpret analytical data, identifying trends or deviations.\nMaintain, calibrate, and troubleshoot laboratory equipment as needed.\nParticipate in investigations related to out-of-specification (OOS) or out-of-trend (OOT) results.\nAssist in the development and revision of SOPs, test methods, and validation protocols.\nEnsure compliance with all applicable regulatory and safety standards (FDA, USP, ICH, etc.).\nCollaborate with other departments such as R&D, Manufacturing, and Quality Assurance to support product release and continuous improvement initiatives.\nQualifications:\nBachelor’s or Master’s degree in Chemistry, Biochemistry, or a related field.\n2–3 years of relevant experience in a QC laboratory within the pharmaceutical industry.\nHands-on experience with analytical instruments (e.g., HPLC, GC, UV-Vis, FTIR).\nKnowledge of USP/NF monographs and pharmaceutical regulatory guidelines (FDA, cGMP, ICH).\nStrong analytical thinking, problem-solving skills, and attention to detail.\nExcellent organizational and time-management abilities.\nProficient in Microsoft Office and Laboratory Information Management Systems (LIMS) is a plus.\n\n#J-18808-Ljbffr","company":"Harba","rawCompany":"harba","city":"Indianapolis","state":"IN","isRemote":false,"isActive":true,"createdAt":"2026-06-17T04:11:46.360Z","occupations":[{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"19-2031.00","title":"Chemists","slug":"chemists"},{"code":"19-4031.00","title":"Chemical Technicians","slug":"chemical-technicians"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325998","title":"All Other Miscellaneous Chemical Product and Preparation Manufacturing","slug":"all-other-miscellaneous-chemical-product-and-preparation-manufacturing"},{"code":"325411","title":"Medicinal and Botanical Manufacturing","slug":"medicinal-and-botanical-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"QC Chemist Pharma Analytics & Method Validation","description":"Job Responsibilities:\nPerform routine chemical analyses using HPLC, GC, UV-Vis, FTIR, titration, and other analytical techniques.\nConduct stability testing and method validations according to ICH guidelines.\nPrepare and standardize laboratory reagents and solutions.\nAccurately document test results in accordance with cGMP requirements and Good Documentation Practices (GDP).\nReview and interpret analytical data, identifying trends or deviations.\nMaintain, calibrate, and troubleshoot laboratory equipment as needed.\nParticipate in investigations related to out-of-specification (OOS) or out-of-trend (OOT) results.\nAssist in the development and revision of SOPs, test methods, and validation protocols.\nEnsure compliance with all applicable regulatory and safety standards (FDA, USP, ICH, etc.).\nCollaborate with other departments such as R&D, Manufacturing, and Quality Assurance to support product release and continuous improvement initiatives.\nQualifications:\nBachelor’s or Master’s degree in Chemistry, Biochemistry, or a related field.\n2–3 years of relevant experience in a QC laboratory within the pharmaceutical industry.\nHands-on experience with analytical instruments (e.g., HPLC, GC, UV-Vis, FTIR).\nKnowledge of USP/NF monographs and pharmaceutical regulatory guidelines (FDA, cGMP, ICH).\nStrong analytical thinking, problem-solving skills, and attention to detail.\nExcellent organizational and time-management abilities.\nProficient in Microsoft Office and Laboratory Information Management Systems (LIMS) is a plus.\n\n#J-18808-Ljbffr","datePosted":"2026-06-17T04:11:46.360Z","dateModified":"2026-06-17T04:11:46.360Z","hiringOrganization":{"@type":"Organization","name":"Harba","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Indianapolis","addressRegion":"IN","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"62ea836e2e751c308f2d7ff7"},"url":"https://jobsearcher.com/jobs/62ea836e2e751c308f2d7ff7"}}