{"schemaVersion":"jobsearcher.job.v1","id":"c5c8f6c83c07ad227a6e154a","url":"https://jobsearcher.com/jobs/c5c8f6c83c07ad227a6e154a","canonicalUrl":"https://jobsearcher.com/jobs/c5c8f6c83c07ad227a6e154a","title":"Quality Analyst I","description":"If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.\nQuality Analyst I Full Time Professional Dallas, TX, US\n2 days ago Requisition ID: 1006\nJOB SUMMARY :\nAs a Quality Analyst, individuals will work as part of the Quality Unit, alongside manufacturing operations, participating in activities such as reviewing and approving planned and unplanned manufacturing events, reviewing processes and suppliers against cGMP requirements, performing testing, and participating in the documentation lifecycle.\nDUTIES & RESPONSIBILITIES :\nCompletes incoming, in process and finished goods analytical testing to ensure all specifications are met.\nDraft, review and approve documentation for planned (change control, protocols, etc.) and unplanned (deviations, corrective maintenance, etc.) laboratory and manufacturing changes/events.\nAnalyze/Review process data to assess trends and propose corrective/preventive actions.\nPerforms Environmental Monitoring of production areas, including sample collection.\nReviews line clearance and setup in production areas prior to the start of a new batch or operation.\nProvides Quality approval and acceptance, including the release of raw materials, components, and finished products/preparations.\nProvides oversight and guidance of MCCPMC staff to ensure cGMP adherence during compounded sterile preparations.\nCollects retention samples and monitors drug storage requirements.\nCompletes other projects and duties as required and/or necessary.\nEDUCATION / TRAINING :\nBachelor's Degree in a Chemistry, Microbiology or related scientific field, or Equivalent years of directly related experience.\nTrained in lab testing processes and procedures.\nKnowledge of USP Sterile and Non-sterile Compounding requirements and FDA regulatory requirements (i.e. 21 CFR and FDA Guidance documents specific to Drug Manufacturing).\nWORK EXPERIENCE :\nMinimum of two (2) years of pharmaceutical experience in a pharmaceutical company or quality role.\nQuality-driven, results oriented, and strong attention to detail.\nProven organizational and time management skills.\nGood computer skills with basic knowledge of Microsoft based programs.\nADDITIONAL QUALIFICATIONS (OPTIONAL):\nAbility to work independently with little to no supervision.\n\n#J-18808-Ljbffr","company":"Evolving Solution Services","rawCompany":"evolving solution services","city":"Dallas","state":"TX","isRemote":false,"isActive":false,"createdAt":"2026-08-08T03:15:00.339Z","occupations":[{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"51-9061.00","title":"Inspectors, Testers, Sorters, Samplers, and Weighers","slug":"inspectors-testers-sorters-samplers-and-weighers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"code":"325411","title":"Medicinal and Botanical Manufacturing","slug":"medicinal-and-botanical-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Quality Analyst I","description":"If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.\nQuality Analyst I Full Time Professional Dallas, TX, US\n2 days ago Requisition ID: 1006\nJOB SUMMARY :\nAs a Quality Analyst, individuals will work as part of the Quality Unit, alongside manufacturing operations, participating in activities such as reviewing and approving planned and unplanned manufacturing events, reviewing processes and suppliers against cGMP requirements, performing testing, and participating in the documentation lifecycle.\nDUTIES & RESPONSIBILITIES :\nCompletes incoming, in process and finished goods analytical testing to ensure all specifications are met.\nDraft, review and approve documentation for planned (change control, protocols, etc.) and unplanned (deviations, corrective maintenance, etc.) laboratory and manufacturing changes/events.\nAnalyze/Review process data to assess trends and propose corrective/preventive actions.\nPerforms Environmental Monitoring of production areas, including sample collection.\nReviews line clearance and setup in production areas prior to the start of a new batch or operation.\nProvides Quality approval and acceptance, including the release of raw materials, components, and finished products/preparations.\nProvides oversight and guidance of MCCPMC staff to ensure cGMP adherence during compounded sterile preparations.\nCollects retention samples and monitors drug storage requirements.\nCompletes other projects and duties as required and/or necessary.\nEDUCATION / TRAINING :\nBachelor's Degree in a Chemistry, Microbiology or related scientific field, or Equivalent years of directly related experience.\nTrained in lab testing processes and procedures.\nKnowledge of USP Sterile and Non-sterile Compounding requirements and FDA regulatory requirements (i.e. 21 CFR and FDA Guidance documents specific to Drug Manufacturing).\nWORK EXPERIENCE :\nMinimum of two (2) years of pharmaceutical experience in a pharmaceutical company or quality role.\nQuality-driven, results oriented, and strong attention to detail.\nProven organizational and time management skills.\nGood computer skills with basic knowledge of Microsoft based programs.\nADDITIONAL QUALIFICATIONS (OPTIONAL):\nAbility to work independently with little to no supervision.\n\n#J-18808-Ljbffr","datePosted":"2026-08-08T03:15:00.339Z","dateModified":"2026-08-08T03:15:00.339Z","hiringOrganization":{"@type":"Organization","name":"Evolving Solution Services","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Dallas","addressRegion":"TX","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"c5c8f6c83c07ad227a6e154a"},"url":"https://jobsearcher.com/jobs/c5c8f6c83c07ad227a6e154a"}}