Job Description
QC Micro Analyst(Shift) RK9989 12 Months Cork Were currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Cork. 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. Duties: Performing a wide variety of microbiology, chemistry or biochemistry testing to support utilities, raw material, in process, bulk and drug product release. Rapid turnaround of samples to meet manufacturing needs. Performing data review and approval. Providing support and advice to manufacturing on QC related topics. Initiating and leading investigations where required. Initiates and completes, CAPAs and Change Controls in accordance with site procedure Writes new and updates current procedures on electronic documentation system. Providing training to other analysts and to manufacturing personnel. Presents technical analytical data clearly and concisely data to customers, i.e., internal investigations and regulatory inspectors etc. Proactively identifies and implements lab process improvements. Supports lean initiatives in the area of lab operations, i.e. standard work, level loading, test method execution, documentation updates and equipment qualification etc. Supports Team leader on day to day testing operations. Education and Experience : The position of QC analyst requires a degree in a science discipline. A minimum of 2 years experience within the Pharmaceutical Industry Knowledgeable of FDA/EMEA regulatory requirements applicable to pharmaceuticals and aseptic products. Experience with Bioburden, Endotoxin, Sterility Testing, Microbial Identification using genetic methods If interested in this posting please feel free to contact Rachel Kent on or for further information. Skills: Microbiology GMP Bioburden and Endotoxin