Job Summary:

We are seeking a QC Material Management Specialist to join the QC Site Operations team at a multi-product cell culture drug substance facility in Dublin for a 12 month contract. Reporting to the QC Material Management Supervisor, the successful candidate will support sample management and laboratory activities in compliance with cGMP regulations. This role is critical to ensuring the timely, accurate processing and control of samples across manufacturing, warehouse, and QC operations.

Key Responsibilities:

Liaise with Manufacturing, Engineering Stores, and Warehouse Cryogenics Logistics to ensure timely processing and delivery of Drug Substance, Drug Product, and Raw Material samples
Manage TempTales and shipping documentation for samples received from external sites
Log samples into LIMS/CIMS or logbooks and ensure accurate labelling
Release samples for QC testing and manage storage of backup and reserve samples
Perform monthly sample reconciliations and report any deviations to the Sample Management Lead
Aliquot samples to support QC activities for Global Biologics Laboratory and the MPCC facility
Support buffer preparation for the QC Separations Laboratory
Generate, review, and update SOPs and other GMP documentation as required
Maintain a high standard of GMP compliance, including completion of all required training
Stay up to date with corporate and industry compliance requirements related to laboratory operations and aseptic manufacturing
Carry out additional duties as assigned by the Lab Supervisor

Key Requirements:

Minimum third-level qualification (Degree) in Chemistry, Biology, or a related discipline
At least 1 year’s experience in a pharmaceutical, healthcare laboratory, or related technical role
Strong knowledge of cGMP principles and laboratory practices
Excellent written and verbal communication skills
Ability to work effectively in a team-based, collaborative environment
Strong attention to detail and organisational skills

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