Position DetailsTullyvin, Cootehill, County CavanNegotiablePermanent | Full TimeContact name: UnivetRole OverviewWe are seeking an experienced and detail‑oriented Microbiology Manager to lead microbiological quality control activities within a veterinary pharmaceutical environment. The successful candidate will oversee sterility assurance programs, environmental monitoring, and microbiological testing while leading the microbiology team and ensuring full regulatory compliance.Key ResponsibilitiesManage and oversee all microbiological testing activities, including:Sterility testing of pharmaceutical productsBioburden testing of raw materials and finished productsEnvironmental monitoring of cleanrooms (air, surfaces, personnel)Settle plates and active air sampling programsEnsure timely and compliant execution of media preparation and growth promotion testing (GPT)Review and approve microbiological data, trend reports, and laboratory resultsMaintain and continuously improve quality documentation, including SOPs, protocols, and test recordsLead investigations related to out‑of‑specification (OOS) results and contamination eventsEnsure compliance with GMP, EU/HPRA/FDA regulatory requirements, and internal quality standardsPeople ManagementLead, coach, and develop the microbiology team to ensure high performance and engagementAllocate workload, manage resources, and ensure appropriate staffing levelsConduct training, performance reviews, and competency assessmentsFoster a culture of quality, accountability, and continuous improvementRegulatory & Audit ResponsibilitiesAct as SME for microbiology during regulatory inspections and customer auditsPrepare and deliver responses to regulatory and customer audit observationsLead audit readiness activities and ensure timely closure of CAPAsEnsure inspection readiness of the microbiology laboratory at all timesDrive continuous improvement initiatives within the microbiology functionRequirementsBachelor’s degree (or higher) in Microbiology, Biological Sciences, or related discipline3–5 years’ experience in a microbiology role within the pharmaceutical or veterinary pharmaceutical industryStrong hands‑on experience with:Sterility testingEnvironmental monitoring (including settle plates)Bioburden testingMedia preparation and growth promotion testingSolid understanding of GMP and regulatory guidelinesExperience in quality documentation and data reviewProven people management or supervisory experienceStrong IT skills, including experience with laboratory systems (e.g., LIMS), data trending, and electronic quality systemsDemonstrated knowledge and experience in responding to regulatory and customer auditsStrong analytical, organisational, and communication skillsDesirableExperience in sterile manufacturing environmentsKnowledge of contamination control strategiesExperience with audit management systems or digital quality platformsWhat We OfferCompetitive salary and benefits packageOpportunity to work in a growing veterinary pharmaceutical companySupportive and collaborative team environmentCareer development and progression opportunities
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