{"schemaVersion":"jobsearcher.job.v1","id":"d905ce7e4b64cfa973b674f5","url":"https://jobsearcher.com/jobs/d905ce7e4b64cfa973b674f5","canonicalUrl":"https://jobsearcher.com/jobs/d905ce7e4b64cfa973b674f5","title":"Cleanroom Microbiologist","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.\n\nCleanroom Microbiologist\nFull Time BOCA RATON, FL, US\n\n2 days ago Requisition ID: 1033\n\n$28.85 To $33.65 Hourly\n\nSummary Statement\n\nThe Cleanroom Microbiologist reports directly to the Cell Processing Supervisor and Scientific Director. This person will be responsible for planning, coordinating, and organizing the overall Quality Control Activities of the Gift of Life Cell and Gene Therapy CNC and cleanrooms.\n\nResponsibilities\n\nPerform tasks associated with maintaining Good Manufacturing Practices (cGMP) compliant Quality Control\n\nPerform environmental testing required for the cleanroom (ISO7 suites)\n\nEvaluate and interpret results of analytical/microbiological testing performed by third parties\n\nWork with the QA department on cleanroom performance qualification.\n\nDevelop an Environmental Monitoring program for GOL cleanrooms.\n\nEstablish sampling plans and collect microbial samples as required.\n\nTrend results of monitoring and determining actions.\n\nResponsible for comprehensive recording of test results.\n\nParticipate in all aspects of cleanroom out of specification, deviations, and contamination event investigations.\n\nEnsure that the necessary microbiology tests are done according to the test specification, test method and working instruction and ensure on time release for cell products.\n\nComplete all required documentation (including, but not limited to, batch records, log books, raw data (charts, graphs, scans, etc.), validation protocols, labels and cGMP-related forms).\n\nMaintain a clean, organized laboratory environment including daily logs and sample tracking\n\nServe as author for qualification protocols and reports for GOL cleanrooms.\n\nPerforms data compilation, review and performs trend analysis on production processes and possible deviations when required.\n\nAssist with manufacturing of cell products, such Hematopoietic Stem Cells and T- cells\n\nPerform Flow cytometry testing (CD34, Viability and B/T cells) as needed\n\nWork closely to QA department and participate in internal and external audits\n\nSupports all lab related tasks\n\nProvides support for projects by attending and participating in team meetings\n\nParticipates in projects, task force jointly with production personnel in case the needs arise\n\nOther duties as assigned by manger\n\nKnowledge, Skills and Experience\n\nExperience with cGMP standards, SOPs, Environmental Health & Safety, and Quality requirements and applicable regulations- maintain awareness of industry best practices\n\nExtensive experience with aseptic techniques\n\nExperience in manufacturing, quality experience in pharmaceutical industry, preferably cell therapy\n\nFamiliarity with standard concepts, practices and procedures in the field of microbiology\n\nExperience with aseptic gowning, environmental monitoring, sterility testing and bacterial endotoxin testing\n\nExperience with Flow Cytometry\n\nCapacity to review and analyze data\n\nExperience defending laboratory practices in regulatory audits\n\nExcellent written communication skills in order to author SOP's, Work Instructions, policies, forms and other documents\n\nGood interpersonal skills\n\nSelf-Starter, team player\n\nAbility to work in a fast-paced controlled cleanroom environment up to 8 hours a day with additional overtime as required.\n\nAbility to work in a cleanroom.\n\nSpecific gowning is required including gloves, hair and beard net and face cover, safety glasses with no makeup, jewelry or piercings.\n\nAbility to use PPE (Personal Protective Equipment) and understand chemical hygiene including labels and SDS (Safety Data Sheets), common chemicals are disinfectant, solvents and IPA (Isopropyl Alcohol 70% and 99%).\n\n#J-18808-Ljbffr","company":"Evolving Solution Services","rawCompany":"evolving solution services","city":"Boca Raton","state":"FL","isRemote":false,"isActive":false,"createdAt":"2026-09-02T04:01:04.449Z","occupations":[{"code":"19-1022.00","title":"Microbiologists","slug":"microbiologists"},{"code":"19-4021.00","title":"Biological Technicians","slug":"biological-technicians"},{"code":"29-2011.00","title":"Medical and Clinical Laboratory Technologists","slug":"medical-and-clinical-laboratory-technologists"}],"industries":[{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"code":"621511","title":"Medical Laboratories","slug":"medical-laboratories"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Cleanroom Microbiologist","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.\n\nCleanroom Microbiologist\nFull Time BOCA RATON, FL, US\n\n2 days ago Requisition ID: 1033\n\n$28.85 To $33.65 Hourly\n\nSummary Statement\n\nThe Cleanroom Microbiologist reports directly to the Cell Processing Supervisor and Scientific Director. This person will be responsible for planning, coordinating, and organizing the overall Quality Control Activities of the Gift of Life Cell and Gene Therapy CNC and cleanrooms.\n\nResponsibilities\n\nPerform tasks associated with maintaining Good Manufacturing Practices (cGMP) compliant Quality Control\n\nPerform environmental testing required for the cleanroom (ISO7 suites)\n\nEvaluate and interpret results of analytical/microbiological testing performed by third parties\n\nWork with the QA department on cleanroom performance qualification.\n\nDevelop an Environmental Monitoring program for GOL cleanrooms.\n\nEstablish sampling plans and collect microbial samples as required.\n\nTrend results of monitoring and determining actions.\n\nResponsible for comprehensive recording of test results.\n\nParticipate in all aspects of cleanroom out of specification, deviations, and contamination event investigations.\n\nEnsure that the necessary microbiology tests are done according to the test specification, test method and working instruction and ensure on time release for cell products.\n\nComplete all required documentation (including, but not limited to, batch records, log books, raw data (charts, graphs, scans, etc.), validation protocols, labels and cGMP-related forms).\n\nMaintain a clean, organized laboratory environment including daily logs and sample tracking\n\nServe as author for qualification protocols and reports for GOL cleanrooms.\n\nPerforms data compilation, review and performs trend analysis on production processes and possible deviations when required.\n\nAssist with manufacturing of cell products, such Hematopoietic Stem Cells and T- cells\n\nPerform Flow cytometry testing (CD34, Viability and B/T cells) as needed\n\nWork closely to QA department and participate in internal and external audits\n\nSupports all lab related tasks\n\nProvides support for projects by attending and participating in team meetings\n\nParticipates in projects, task force jointly with production personnel in case the needs arise\n\nOther duties as assigned by manger\n\nKnowledge, Skills and Experience\n\nExperience with cGMP standards, SOPs, Environmental Health & Safety, and Quality requirements and applicable regulations- maintain awareness of industry best practices\n\nExtensive experience with aseptic techniques\n\nExperience in manufacturing, quality experience in pharmaceutical industry, preferably cell therapy\n\nFamiliarity with standard concepts, practices and procedures in the field of microbiology\n\nExperience with aseptic gowning, environmental monitoring, sterility testing and bacterial endotoxin testing\n\nExperience with Flow Cytometry\n\nCapacity to review and analyze data\n\nExperience defending laboratory practices in regulatory audits\n\nExcellent written communication skills in order to author SOP's, Work Instructions, policies, forms and other documents\n\nGood interpersonal skills\n\nSelf-Starter, team player\n\nAbility to work in a fast-paced controlled cleanroom environment up to 8 hours a day with additional overtime as required.\n\nAbility to work in a cleanroom.\n\nSpecific gowning is required including gloves, hair and beard net and face cover, safety glasses with no makeup, jewelry or piercings.\n\nAbility to use PPE (Personal Protective Equipment) and understand chemical hygiene including labels and SDS (Safety Data Sheets), common chemicals are disinfectant, solvents and IPA (Isopropyl Alcohol 70% and 99%).\n\n#J-18808-Ljbffr","datePosted":"2026-09-02T04:01:04.449Z","dateModified":"2026-09-02T04:01:04.449Z","hiringOrganization":{"@type":"Organization","name":"Evolving Solution Services","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Boca Raton","addressRegion":"FL","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"d905ce7e4b64cfa973b674f5"},"url":"https://jobsearcher.com/jobs/d905ce7e4b64cfa973b674f5"}}