QC Material Management - Dublin, Ireland - 12-Month Contract
Our client is seeking to recruit a QC Material Management Analyst to join the QC Site Operations team at its Multi-Product Cell Culture Drug Substance Facility in Dublin.
Reporting to the QC Material Management Supervisor, they will be responsible for supporting site activities related to the Sample Management/Buffer Preparation Laboratory, in-process samples, and laboratory duties in accordance with cGMP regulations.
The main responsibilities for this position include;
- 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.
- Buffer preparation activities for the QC Laboratories.
- 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
If this role is of interest to you, please apply now!
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