Quality Control Microbiologist

🔬 QC Microbiology Specialist📍 Location: Athlone, Co. Westmeath, IrelandWe're currently recruiting for an experienced QC Microbiology Specialist to join a leading pharmaceutical manufacturing site in Athlone. This is an excellent opportunity to work in a GMP-regulated sterile manufacturing environment, supporting critical quality control activities that help ensure the safety and quality of life-changing medicines.About the RoleAs a QC Microbiology Specialist, you'll play a key role in supporting sterile manufacturing through environmental monitoring, water and microbial testing, laboratory investigations, validation activities, and sterility assurance. You'll work closely with Manufacturing, Quality, and Technical teams to maintain the highest standards of GMP compliance and product quality.Key ResponsibilitiesPerform environmental monitoring of cleanroom manufacturing areasConduct water, utility, and microbial testing, including:Bioburden testingEndotoxin testingTOC and conductivity testingGrowth promotion testingBiological indicator testingBacterial identificationExecute process and method validation protocolsSupport laboratory investigations and root cause analysis using structured problem-solving techniquesReview laboratory data and GMP documentationMaintain laboratory equipment and ensure compliance with GMP requirementsDevelop and support laboratory procedures and site documentationDeliver sterility assurance and microbiology awareness trainingParticipate in media fill studies to support sterile manufacturing qualificationEscalate quality, safety, or compliance risks where appropriateWhat We're Looking ForDegree in Microbiology or a related Life Sciences disciplineMinimum 5 years' experience in a cGMP Quality Control Microbiology laboratoryAt least 2 years' experience within the pharmaceutical industryHands-on experience with microbiological testing in sterile manufacturing environmentsExperience performing environmental monitoring and utility testingStrong understanding of sterility assurance principles and current GMP regulationsExperience with method validation and quality risk managementExcellent attention to detail, documentation, and problem-solving skillsWhy Apply?Join a highly regulated, modern pharmaceutical manufacturing facilityWork with an experienced Quality team supporting sterile manufacturingOpportunity to contribute to patient safety through critical quality operationsCollaborative team environment with ongoing learning and development opportunities