{"schemaVersion":"jobsearcher.job.v1","id":"37772da99bc345d8241978e9","url":"https://jobsearcher.com/jobs/37772da99bc345d8241978e9","canonicalUrl":"https://jobsearcher.com/jobs/37772da99bc345d8241978e9","title":"Scientist III","description":"Salary Range: $85,000 - $95,000/yr DOE\nJOB QUALIFICATIONS:\nBS/MS in Chemistry or related Scientific Discipline with a minimum of 8 years of pharmaceutical experience or equivalent combination of education and experience with testing Finished Products, Raw Materials, and Analytical Method Verification, Validations and Transfers.\nAdvanced technical skills in HPLC and GC required, including theoretical understanding of technique, troubleshooting, maintenance and consumable replacements.\nAdvanced level of Chromatography Data Software (CDS) preferably Empower 3.\nAbility to enable quantification for assays and impurities calculations, create custom calculations, and design chromatographic reports in CDS.\nAble to interpret data, including evaluation of stability testing for trends.\nDemonstrated use of analytical techniques in support of product development activities.\nComprehensive knowledge of current Good Manufacturing Practices (cGMP), regulatory requirements, and ICH Guidelines\nUnderstanding and adherence with CFR 21 Part 11 requirements.\nUnderstanding, Knowledge, and performing of Raw Material qualifications of new incoming raw materials along with annual review requirements for existing Raw Materials.\nComprehension and ability to follow procedures of various pharmacopeias (USP, EP, JP).\nComprehension of regulated guidance (WHO, FCC, FDA, and ICH)\nUnderstanding and basic regulatory requirements and applies knowledge appropriately to activities.\nDemonstrated ability to work well in a fast-paced setting with teams.\nSelf-starter with a strong work ethic.\nMust possess problem solving skills.\nMust be able to operate with minimal supervision.\nDemonstrated ability to train and/or mentor employees.\nExcellent written and verbal communication skills.\n\nPOSITION RESPONSIBILITIES:\nThe Ability to analyze Finish Good Products and Raw Materials on HPLC, GC, FTIR, and Titrations (visual and potentiometric).\nAbility to manage multiple projects and accurately project realistic timelines.\nAbility to Qualify Raw Materials by compendial testing procedures.\nAuthors Analytical Method Validation or Method Verification Protocols as guided by ICH, FDA, and cUSP.\nResponsible for analytical method validation/verification/transfer from clients or R&D to QC when assigned.\nPerforms testing on raw material, in-process, & finished good samples when applicable.\nDocuments all data in corresponding laboratory notebook and files documentation according to approved SOP and data integrity guidelines.\nInterface with contract labs regarding QC sample handling and reporting.\nEvaluate and interpret the test results and other related technical documentation.\nAdditional document writing includes, but not limited to, preparation and review of SOPs, STMs, failure investigation and process deviation report, stability study protocol/report, instrument qualification protocol/report and analytical technical transfer protocol/report.\nOther duties may be assigned as deemed appropriate by management.\nMentors QC chemists and assists with training and professional development.\nUpholds all elements of data integrity.\n\nPHYSICAL REQUIREMENTS:\nEmployees are required to wear eye protection and lab coats while in the lab area.\nWork safely and follow all OSHA regulations and company safety policies and procedures.\nAbility to frequently lift and/or move up to 25 lb.\nAbility to occasionally lift and/or move up to 35 lb.\nAbility to regularly stand, sit and walk to perform tasks.\nEducation\nRequired\nBachelors or better in Chemistry or related field","company":"Pl Developments","rawCompany":"pl developments","city":"Garden Grove","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-04-12T20:27:07.203Z","occupations":[{"code":"19-4031.00","title":"Chemical Technicians","slug":"chemical-technicians"},{"code":"19-2031.00","title":"Chemists","slug":"chemists"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"}],"industries":[{"code":"325998","title":"All Other Miscellaneous Chemical Product and Preparation Manufacturing","slug":"all-other-miscellaneous-chemical-product-and-preparation-manufacturing"},{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"541715","title":"Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)","slug":"research-and-development-in-the-physical-engineering-and-life-sciences-except-nanotechnology-and-biotechnology"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Scientist III","description":"Salary Range: $85,000 - $95,000/yr DOE\nJOB QUALIFICATIONS:\nBS/MS in Chemistry or related Scientific Discipline with a minimum of 8 years of pharmaceutical experience or equivalent combination of education and experience with testing Finished Products, Raw Materials, and Analytical Method Verification, Validations and Transfers.\nAdvanced technical skills in HPLC and GC required, including theoretical understanding of technique, troubleshooting, maintenance and consumable replacements.\nAdvanced level of Chromatography Data Software (CDS) preferably Empower 3.\nAbility to enable quantification for assays and impurities calculations, create custom calculations, and design chromatographic reports in CDS.\nAble to interpret data, including evaluation of stability testing for trends.\nDemonstrated use of analytical techniques in support of product development activities.\nComprehensive knowledge of current Good Manufacturing Practices (cGMP), regulatory requirements, and ICH Guidelines\nUnderstanding and adherence with CFR 21 Part 11 requirements.\nUnderstanding, Knowledge, and performing of Raw Material qualifications of new incoming raw materials along with annual review requirements for existing Raw Materials.\nComprehension and ability to follow procedures of various pharmacopeias (USP, EP, JP).\nComprehension of regulated guidance (WHO, FCC, FDA, and ICH)\nUnderstanding and basic regulatory requirements and applies knowledge appropriately to activities.\nDemonstrated ability to work well in a fast-paced setting with teams.\nSelf-starter with a strong work ethic.\nMust possess problem solving skills.\nMust be able to operate with minimal supervision.\nDemonstrated ability to train and/or mentor employees.\nExcellent written and verbal communication skills.\n\nPOSITION RESPONSIBILITIES:\nThe Ability to analyze Finish Good Products and Raw Materials on HPLC, GC, FTIR, and Titrations (visual and potentiometric).\nAbility to manage multiple projects and accurately project realistic timelines.\nAbility to Qualify Raw Materials by compendial testing procedures.\nAuthors Analytical Method Validation or Method Verification Protocols as guided by ICH, FDA, and cUSP.\nResponsible for analytical method validation/verification/transfer from clients or R&D to QC when assigned.\nPerforms testing on raw material, in-process, & finished good samples when applicable.\nDocuments all data in corresponding laboratory notebook and files documentation according to approved SOP and data integrity guidelines.\nInterface with contract labs regarding QC sample handling and reporting.\nEvaluate and interpret the test results and other related technical documentation.\nAdditional document writing includes, but not limited to, preparation and review of SOPs, STMs, failure investigation and process deviation report, stability study protocol/report, instrument qualification protocol/report and analytical technical transfer protocol/report.\nOther duties may be assigned as deemed appropriate by management.\nMentors QC chemists and assists with training and professional development.\nUpholds all elements of data integrity.\n\nPHYSICAL REQUIREMENTS:\nEmployees are required to wear eye protection and lab coats while in the lab area.\nWork safely and follow all OSHA regulations and company safety policies and procedures.\nAbility to frequently lift and/or move up to 25 lb.\nAbility to occasionally lift and/or move up to 35 lb.\nAbility to regularly stand, sit and walk to perform tasks.\nEducation\nRequired\nBachelors or better in Chemistry or related field","datePosted":"2026-04-12T20:27:07.203Z","dateModified":"2026-04-12T20:27:07.203Z","hiringOrganization":{"@type":"Organization","name":"Pl Developments","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Garden Grove","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"37772da99bc345d8241978e9"},"url":"https://jobsearcher.com/jobs/37772da99bc345d8241978e9"}}