{"schemaVersion":"jobsearcher.job.v1","id":"ef6a849c5b3a119ebcb0800c","url":"https://jobsearcher.com/jobs/ef6a849c5b3a119ebcb0800c","canonicalUrl":"https://jobsearcher.com/jobs/ef6a849c5b3a119ebcb0800c","title":"Quality Control Chemist","description":"Position Summary\n\nA rapidly growing specialty pharmaceutical company is seeking all levels of experienced Quality Control Chemists (I, II, Sr.) . This role is responsible for performing analytical testing of pharmaceutical raw materials, in-process samples, stability samples, and finished drug products to ensure compliance with regulatory requirements and internal quality standards. This role supports product quality, patient safety, and regulatory compliance through laboratory testing, method execution, investigations, and continuous improvement initiatives.\n\nKey Responsibilities\n\nPerform qualitative and quantitative analysis of raw materials, intermediates, and finished pharmaceutical products using validated analytical methods.\n\nOperate, maintain, and troubleshoot laboratory instrumentation including HPLC, UPLC, GC, GC‑MS, LC‑MS, FTIR, UV‑Vis, dissolution systems, and related equipment.\n\nExecute testing in accordance with approved specifications, SOPs, cGMP requirements, and regulatory guidelines.\n\nConduct stability testing and support stability programs in accordance with ICH guidelines.\n\nAssist with analytical method development, verification, transfer, and validation activities.\n\nMaintain accurate laboratory notebooks, test records, electronic data, and documentation in compliance with data integrity requirements.\n\nInvestigate laboratory deviations, out‑of‑specification (OOS) results, and atypical findings.\n\nParticipate in root cause analysis and support corrective and preventive action (CAPA) activities.\n\nPerform routine calibration, qualification, and preventive maintenance of laboratory equipment.\n\nSupport internal audits, customer audits, and regulatory inspections.\n\nCollaborate with Quality Assurance, Manufacturing, Validation, and R&D teams to support product development and commercial operations.\n\nFollow all applicable Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), and company quality procedures.\n\nPerform additional duties as assigned.\n\nQualifications\n\nAssociate of Science (A.S.) Chemistry, Pharmaceutical Sciences, Biochemistry, or a related scientific discipline, plus 2 years of industry experience.\n\nBachelor's or Master’s degree preferred.\n\nExperience\n\n1‑8 years of pharmaceutical quality control laboratory experience levels (I – Senior).\n\nExperience working in an FDA‑regulated cGMP environment.\n\nExperience supporting generic pharmaceutical, sterile, or oral solid dosage manufacturing environments preferred.\n\nTechnical Skills\n\nHands‑on experience with:\n\nHPLC\n\nUPLC\n\nGas Chromatography (GC)\n\nFTIR Spectroscopy\n\nUV‑Visible Spectroscopy\n\nDissolution Testing\n\nLC‑MS and/or GC‑MS\n\nKnowledge of FDA regulations, cGMP requirements, and ICH guidelines.\n\nFamiliarity with ICH Q1 (Stability), ICH Q2 (Method Validation), ICH Q7, and pharmaceutical quality systems.\n\nStrong troubleshooting and analytical problem‑solving skills.\n\nExperience with OOS investigations, deviations, CAPA, and change control processes.\n\nBenefits\n\nCompetitive salary\n\nMedical, dental, and vision insurance\n\n401(k) plan\n\nPaid time off\n\nEstimated Min Rate: $80,500.00 Estimated Max Rate: $115,000.00\n\nNote: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.\n\nYoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.\n\nVisit https://www.yoh.com/applicants-with-disabilities to contact us if you are an individual with a disability and require accommodation in the application process.\n\n#J-18808-Ljbffr","company":"Yoh","rawCompany":"yoh","city":"Sacramento","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-06-20T04:55:32.534Z","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":"Quality Control Chemist","description":"Position Summary\n\nA rapidly growing specialty pharmaceutical company is seeking all levels of experienced Quality Control Chemists (I, II, Sr.) . This role is responsible for performing analytical testing of pharmaceutical raw materials, in-process samples, stability samples, and finished drug products to ensure compliance with regulatory requirements and internal quality standards. This role supports product quality, patient safety, and regulatory compliance through laboratory testing, method execution, investigations, and continuous improvement initiatives.\n\nKey Responsibilities\n\nPerform qualitative and quantitative analysis of raw materials, intermediates, and finished pharmaceutical products using validated analytical methods.\n\nOperate, maintain, and troubleshoot laboratory instrumentation including HPLC, UPLC, GC, GC‑MS, LC‑MS, FTIR, UV‑Vis, dissolution systems, and related equipment.\n\nExecute testing in accordance with approved specifications, SOPs, cGMP requirements, and regulatory guidelines.\n\nConduct stability testing and support stability programs in accordance with ICH guidelines.\n\nAssist with analytical method development, verification, transfer, and validation activities.\n\nMaintain accurate laboratory notebooks, test records, electronic data, and documentation in compliance with data integrity requirements.\n\nInvestigate laboratory deviations, out‑of‑specification (OOS) results, and atypical findings.\n\nParticipate in root cause analysis and support corrective and preventive action (CAPA) activities.\n\nPerform routine calibration, qualification, and preventive maintenance of laboratory equipment.\n\nSupport internal audits, customer audits, and regulatory inspections.\n\nCollaborate with Quality Assurance, Manufacturing, Validation, and R&D teams to support product development and commercial operations.\n\nFollow all applicable Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), and company quality procedures.\n\nPerform additional duties as assigned.\n\nQualifications\n\nAssociate of Science (A.S.) Chemistry, Pharmaceutical Sciences, Biochemistry, or a related scientific discipline, plus 2 years of industry experience.\n\nBachelor's or Master’s degree preferred.\n\nExperience\n\n1‑8 years of pharmaceutical quality control laboratory experience levels (I – Senior).\n\nExperience working in an FDA‑regulated cGMP environment.\n\nExperience supporting generic pharmaceutical, sterile, or oral solid dosage manufacturing environments preferred.\n\nTechnical Skills\n\nHands‑on experience with:\n\nHPLC\n\nUPLC\n\nGas Chromatography (GC)\n\nFTIR Spectroscopy\n\nUV‑Visible Spectroscopy\n\nDissolution Testing\n\nLC‑MS and/or GC‑MS\n\nKnowledge of FDA regulations, cGMP requirements, and ICH guidelines.\n\nFamiliarity with ICH Q1 (Stability), ICH Q2 (Method Validation), ICH Q7, and pharmaceutical quality systems.\n\nStrong troubleshooting and analytical problem‑solving skills.\n\nExperience with OOS investigations, deviations, CAPA, and change control processes.\n\nBenefits\n\nCompetitive salary\n\nMedical, dental, and vision insurance\n\n401(k) plan\n\nPaid time off\n\nEstimated Min Rate: $80,500.00 Estimated Max Rate: $115,000.00\n\nNote: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.\n\nYoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.\n\nVisit https://www.yoh.com/applicants-with-disabilities to contact us if you are an individual with a disability and require accommodation in the application process.\n\n#J-18808-Ljbffr","datePosted":"2026-06-20T04:55:32.534Z","dateModified":"2026-06-20T04:55:32.534Z","hiringOrganization":{"@type":"Organization","name":"Yoh","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Sacramento","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"ef6a849c5b3a119ebcb0800c"},"url":"https://jobsearcher.com/jobs/ef6a849c5b3a119ebcb0800c"}}