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HomeCompaniesA75f8631 1c72 434e 940f Abf13d0db5c3 19000101 000001Microbiologist Manager

Microbiologist Manager

A75f8631 1c72 434e 940f Abf13d0db5c3 19000101 000001 · Chandler, AZ, US, Chandler, AZ · Active · $80,000–$90,000 / year · ADP Workforce Now Recruiting

Job facts

FieldValue
CompanyA75f8631 1c72 434e 940f Abf13d0db5c3 19000101 000001
TitleMicrobiologist Manager
Normalized title-
Department / team-
LocationChandler, AZ, United States
Work model-
Employment typeFull Time
Salary$80,000–$90,000 / year
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-04-27 / 2026-05-31
Changed / last seen2026-06-06 / 2026-06-06

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PageWhat it containsOpen
Company jobsActive postings from A75f8631 1c72 434e 940f Abf13d0db5c3 19000101 000001.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through ADP Workforce Now Recruiting.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Chandler.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyA75f8631 1c72 434e 940f Abf13d0db5c3 19000101 000001
Source6b819f52-a876-47c7-ab03-aa82df48c757
ATS providerADP Workforce Now Recruiting

Description

Position Summary The Microbiology Manager is responsible for leading and overseeing all microbiological operations within Medivant’s 503B pharmaceutical outsourcing facilities. This role ensures compliance with FDA regulations, cGMP standards, USP requirements, and internal quality systems while supporting sterile manufacturing through effective environmental control, microbiological testing, contamination prevention, and continuous improvement initiatives. The ideal candidate will provide leadership to the microbiology team, maintain inspection readiness, and collaborate cross-functionally with Quality Assurance, Manufacturing, and Validation teams to ensure product quality and regulatory compliance. Key Responsibilities Provide leadership and oversight for all microbiological programs including Environmental Monitoring (EM), Personnel Monitoring (PM), Sterility Testing, Endotoxin Testing (BET), Bioburden Testing, and Microbial Identification. Supervise, train, mentor, and develop microbiology staff while ensuring adherence to cGMP standards, aseptic practices, and ISO cleanroom requirements. Review, approve, and trend microbiological data including EM/PM results, sterility testing outcomes, and microbial identification reports. Lead investigations related to OOS, OOT, contamination events, and environmental excursions, ensuring timely closure and implementation of CAPAs. Support qualification and validation activities including microbiological methods, disinfectant efficacy studies, sterilization cycles, and cleanroom controls. Partner closely with Quality Assurance and Manufacturing teams to provide microbiological guidance for aseptic processing and contamination control strategies. Serve as Subject Matter Expert (SME) during FDA inspections, customer audits, and regulatory reviews. Ensure laboratory readiness through proper inventory management of media, reagents, consumables, and equipment. Develop, review, and approve SOPs, protocols, validation reports, and technical documentation related to microbiology operations. Maintain training programs to ensure staff competency, compliance awareness, and aseptic qualification standards. Evaluate and implement new technologies, testing methods, and process improvements to enhance quality, efficiency, and compliance. Promote a culture of safety, quality, accountability, and data integrity (ALCOA+ principles). Qualifications Required: Bachelor’s degree in Microbiology, Biology, or related scientific field. 6–10+ years of pharmaceutical microbiology experience, preferably within sterile manufacturing or 503B outsourcing facilities. Strong knowledge of cGMP regulations and USP chapters including , , , , , and / as applicable. Proven experience managing microbiology laboratory operations, environmental monitoring programs, sterility assurance, and investigations. Hands-on experience with CAPAs, Change Controls, Deviations, OOS/OOT investigations, and audit readiness. Strong leadership, communication, organizational, and technical writing skills. Preferred: Master’s degree in Microbiology, Biology, or related scientific field. Experience with electronic Quality Management Systems such as MasterControl, Progen, or similar platforms. Previous experience supporting FDA inspections or regulatory audits in a pharmaceutical environment. Key Competencies Leadership & Team Development Regulatory Compliance & Inspection Readiness Technical Expertise in Microbiology Problem Solving & Root Cause Analysis Data Integrity & Quality Focus Cross-Functional Collaboration Continuous Improvement Mindset Please note that we are not providing H1B visa sponsorship for this role. Candidates will be solely responsible for managing and maintaining their own visa sponsorship status.

Full job record

Job ID62dc701dcfee9b76b3d68ebab77f1dfeae5a6d50
Org ID23904bd9-e730-4f80-9581-79cb269873da
Source ID6b819f52-a876-47c7-ab03-aa82df48c757
Board ID6b819f52-a876-47c7-ab03-aa82df48c757
Provideradp_workforcenow
Provider Job Key567823
TitleMicrobiologist Manager
Normalized Title
Statusactive
Activeyes
Location TextChandler, AZ, US, Chandler, AZ
Department
Team
Employment Typefull_time
Workplace Type
Remote Policy
CountryUnited States
RegionAZ
CityChandler
Salary Raw80000.00 To 90000.00 (USD) Annually
Salary Min80,000
Salary Max90,000
Salary CurrencyUSD
Salary Periodyear
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First Seen At2026-05-31 18:34:48Z
Last Seen At2026-06-06 12:44:43Z
Last Checked At2026-06-06 12:44:43Z
Last Changed At2026-06-06 12:44:43Z
Inactive At
Source Posted At2026-04-27 17:16:00Z
Source Updated At
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This role ensures compliance with FDA regulations, cGMP standards, USP requirements, and internal quality systems while supporting sterile manufacturing through effective environmental control, microbiological testing, contamination prevention, and continuous improvement initiatives.</p><p data-start=\"1039\" data-end=\"1289\">The ideal candidate will provide leadership to the microbiology team, maintain inspection readiness, and collaborate cross-functionally with Quality Assurance, Manufacturing, and Validation teams to ensure product quality and regulatory compliance.</p><p data-start=\"1039\" data-end=\"1289\"><br></p><p data-start=\"1291\" data-end=\"1317\"><strong data-start=\"1291\" data-end=\"1315\">Key Responsibilities</strong></p><p data-start=\"1319\" data-end=\"1547\">Provide leadership and oversight for all microbiological programs including Environmental Monitoring (EM), Personnel Monitoring (PM), Sterility Testing, Endotoxin Testing (BET), Bioburden Testing, and Microbial Identification.</p><p data-start=\"1549\" data-end=\"1702\">Supervise, train, mentor, and develop microbiology staff while ensuring adherence to cGMP standards, aseptic practices, and ISO cleanroom requirements.</p><p data-start=\"1704\" data-end=\"1844\">Review, approve, and trend microbiological data including EM/PM results, sterility testing outcomes, and microbial identification reports.</p><p data-start=\"1846\" data-end=\"1993\">Lead investigations related to OOS, OOT, contamination events, and environmental excursions, ensuring timely closure and implementation of CAPAs.</p><p data-start=\"1995\" data-end=\"2156\">Support qualification and validation activities including microbiological methods, disinfectant efficacy studies, sterilization cycles, and cleanroom controls.</p><p data-start=\"2158\" data-end=\"2319\">Partner closely with Quality Assurance and Manufacturing teams to provide microbiological guidance for aseptic processing and contamination control strategies.</p><p data-start=\"2321\" data-end=\"2424\">Serve as Subject Matter Expert (SME) during FDA inspections, customer audits, and regulatory reviews.</p><p data-start=\"2426\" data-end=\"2539\">Ensure laboratory readiness through proper inventory management of media, reagents, consumables, and equipment.</p><p data-start=\"2541\" data-end=\"2672\">Develop, review, and approve SOPs, protocols, validation reports, and technical documentation related to microbiology operations.</p><p data-start=\"2674\" data-end=\"2789\">Maintain training programs to ensure staff competency, compliance awareness, and aseptic qualification standards.</p><p data-start=\"2791\" data-end=\"2923\">Evaluate and implement new technologies, testing methods, and process improvements to enhance quality, efficiency, and compliance.</p><p data-start=\"2925\" data-end=\"3020\">Promote a culture of safety, quality, accountability, and data integrity (ALCOA+ principles).</p><p data-start=\"2925\" data-end=\"3020\"><br></p><p data-start=\"3022\" data-end=\"3042\"><strong data-start=\"3022\" data-end=\"3040\">Qualifications</strong></p><p data-start=\"3044\" data-end=\"3059\"><strong data-start=\"3044\" data-end=\"3057\">Required:</strong></p><p data-start=\"3061\" data-end=\"3135\">Bachelor&rsquo;s degree in Microbiology, Biology, or related scientific field.</p><p data-start=\"3137\" data-end=\"3265\">6&ndash;10+ years of pharmaceutical microbiology experience, preferably within sterile manufacturing or 503B outsourcing facilities.</p><p data-start=\"3267\" data-end=\"3395\">Strong knowledge of cGMP regulations and USP chapters including &lt;71&gt;, &lt;61&gt;, &lt;62&gt;, &lt;85&gt;, &lt;1116&gt;, and &lt;797&gt;/&lt;800&gt; as applicable.</p><p data-start=\"3397\" data-end=\"3537\">Proven experience managing microbiology laboratory operations, environmental monitoring programs, sterility assurance, and investigations.</p><p data-start=\"3539\" data-end=\"3646\">Hands-on experience with CAPAs, Change Controls, Deviations, OOS/OOT investigations, and audit readiness.</p><p data-start=\"3648\" data-end=\"3729\">Strong leadership, communication, organizational, and technical writing skills.</p><p data-start=\"3731\" data-end=\"3747\"><strong data-start=\"3731\" data-end=\"3745\">Preferred:</strong></p><p data-start=\"3749\" data-end=\"3821\">Master&rsquo;s degree in Microbiology, Biology, or related scientific field.</p><p data-start=\"3823\" data-end=\"3931\">Experience with electronic Quality Management Systems such as MasterControl, Progen, or similar platforms.</p><p data-start=\"3933\" data-end=\"4035\">Previous experience supporting FDA inspections or regulatory audits in a pharmaceutical environment.</p><p data-start=\"3933\" data-end=\"4035\"><br></p><p data-start=\"4037\" data-end=\"4059\"><strong data-start=\"4037\" data-end=\"4057\">Key Competencies</strong></p><p data-start=\"4061\" data-end=\"4092\">Leadership &amp; Team Development</p><p data-start=\"4094\" data-end=\"4140\">Regulatory Compliance &amp; Inspection Readiness</p><p data-start=\"4142\" data-end=\"4179\">Technical Expertise in Microbiology</p><p data-start=\"4181\" data-end=\"4220\">Problem Solving &amp; Root Cause Analysis</p><p data-start=\"4222\" data-end=\"4254\">Data Integrity &amp; Quality Focus</p><p data-start=\"4256\" data-end=\"4288\">Cross-Functional Collaboration</p><p data-start=\"4290\" data-end=\"4320\" data-is-last-node=\"\" data-is-only-node=\"\">Continuous Improvement Mindset</p></div></section><p><br></p><p><span data-teams=\"true\" data-pasted=\"true\"><strong>Please note that we are not providing H1B visa sponsorship for this role. 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