Role Title:QC Material Management AnalystRole Type:12 Month ContractLocation:Dublin 15We are currently recruiting a QC Material Management Analyst to join a QC Site Operations team at a Biopharmaceutical Manufacturer in Dublin 15. Reporting to the QC Material Management Supervisor, they will be responsible for supporting site activities related to Sample Management Laboratory, in-process samples, and laboratory duties in accordance with cGMP regulations.Responsibilities:• Liaise with manufacturing to ensure all Drug Substance samples are processed and delivered to the appropriate destination in an appropriate timeframe.• Liaise with Engineering Stores to ensure all Drug Product samples are processed and delivered to the appropriate destination in an appropriate timeframe.• Liaise with Warehouse Cryogenics Logistics (WCL) to ensure all Raw Material samples are processed and delivered to the appropriate destination in an appropriate timeframe.• Manage TempTales and shipping documents when receiving samples from external sites.• Log in of samples to LIMS/CIMS or logbooks, and label accordingly.• Release samples for QC testing.• Storage of backups and reserve samples.• Perform monthly reconciliation and report deviations to Sample Management Lead, if any.• Aliquot samples for the QC activities for Global Biologics Laboratory and Multi Product Cell Culture (MPCC) Facility.• Support buffer preparation for the QC Separations lab• Generate and update SOPs and other relevant documents as required.• Maintain a high standard of GMP compliance including the completion and provision of training as required.• Keeps abreast of current corporate and industry requirements and compliance trends as they pertain to laboratory operations and aseptic manufacturing.• Performing any other activities as indicated by the Lab Supervisor.The successful candidate must demonstrate excellent written and verbal communication skills and the ability to work in a team based collaborative environment.The ideal candidate should hold a minimum of a third level qualification (Degree) in Chemistry/Biology or related discipline along with at least 1 year of experience in a pharmaceutical / healthcare laboratory or related technical function.