Are you an experienced QC Micro Analyst who specialises in Environmental Monitoring within your current role and you're looking for an exciting new role where you will support manufacturing operations during the qualification of new clean rooms. This is a 4 Cycle shift position, 2 days 7am – 7pm followed by 2 nights 7pm – 7am with a 35% shift allowance.18 month contract with specific duties such as:Environmental Monitoring of Grade 8/9 CleanroomsEnvironmental Monitoring of Grade 5/7 Cleanrooms & IsolatorsReading of Environmental Monitoring PlatesBioburden testing of water & disinfectantsWriting technical reportsWater samplingTesting of In Process samples such as Protein Concentration, Density & pHQualifications & ExperienceBachelor's degree in a science disciplineBiopharmaceutical QC experience in a microbiology labExperience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical productsExperience working in an aseptic cleanroom performing Environmental MonitoringProficient in the use of LIMS & LMESCore CompetenciesTechnically strong background in microbiology and aseptic manufacturingExperience in LIMS, Change Control, Trackwise, SAP and CDOCS an advantageFlexibility – the EM role often encounters changing priorities on a daily basisExperience with Regulatory inspectors and interacting with inspectors desirableDemonstrated ability to work independently and deliver right first time resultsWork is guided by objectives of the department or assignmentRefers to technical standards, principles, theories and precedents as neededMay set project timeframes and priorities based on project objectives and ongoing assignments.Recognises and escalates problemsDemonstrated leadership and communication skillsAuditing documentation and operation processDemonstrated ability to interact with regulatory agencies