Were currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Dublin. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Ideally the person will be responsible for one or more of the following activities in QC including microbiological testing, method transfers, sample and data management and equipment maintenance. This role is for an experienced and technically strong associate who will spend 90% of their work day performing testing. This role will support manufacturing operations on a 24/7 shift pattern and may include extended hours. Responsible for: 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 Writing technical reports Water sampling Testing of In Process samples such as Density & pH 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 Problem solving skills Experience with Regulatory inspectors and interacting with inspectors desirable Demonstrated ability to work independently and deliver right first time results Works under minimal direction Work is guided by objectives of the department or assignment Follows procedures Refers to technical standards, principles, theories and precedents as needed May set project timeframes and priorities based on project objectives and ongoing assignments. Recognizes and escalates problems Demonstrated leadership and communication skills Auditing documentation and operation process Demonstrated ability to interact with regulatory agencies Education and Skills: Bachelors degree in a science discipline?with 2+ years of experience in the pharma or biopharma industry. Biopharmaceutical QC experience in a 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 If interested in this posting please feel free to contact Avishek Singh at Avishek.sing or for further information.