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. This is a 4 Cycle shift position, 2 days 7am - 7pm followed by 2 nights 7pm - 7am with a 35% shift allowance. 12 month contract Duties will include: Environmental Monitoring of Grade 8/9 Cleanrooms Environmental Monitoring of Grade 5/7 Cleanrooms & Isolators Reading of Environmental Monitoring Plates Bioburden testing of water & disinfectants as required Writing technical reports Water sampling Testing of In Process samples such as Protein Concentration, Density & pH Qualifications & Experience Bachelor's degree in a science discipline Biopharmaceutical QC experience in Environmental Monitoring within a GMP microbiology lab Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products Experience working in an aseptic cleanroom performing Environmental Monitoring Proficient in the use of LIMS & LMES Core Competencies Technically strong background in microbiology and aseptic manufacturing Experience in LIMS, Change Control, Trackwise, SAP and CDOCS an advantage Flexibility - the EM role often encounters changing priorities on a daily basis Experience with Regulatory inspectors and interacting with inspectors desirable Demonstrated ability to work independently and deliver right first time results Work is guided by objectives of the department or assignment Refers to technical standards, principles, theories and precedents as needed May set project timeframes and priorities based on project objectives and ongoing assignments. Recognises and escalates problems Demonstrated leadership and communication skills Auditing documentation and operation process Demonstrated ability to interact with regulatory agencies Skills: Environmental Monitoring cleanrooms grade A - D microbiology autoclaves sterile plate reads