Overview
Our client is seeking a
QC Material Management Analyst
to join the QC Site Operations team at its facility in Cruiserath, Dublin 15.
This is an exciting opportunity to contribute to a world-class biopharmaceutical company dedicated to transforming patients' lives through science.
Reporting to the QC Material Management Supervisor, you will play a key role in supporting site activities related to testing of raw materials, in-process samples, and laboratory duties — all in accordance with cGMP regulations.
You will also be involved in sample management, documentation, and supporting technical transfers.
Responsibilities
Perform QC testing of water samples (TOC, pH, Conductivity).
Analyse raw materials using HPLC, KF, UV, IR, and wet chemistry techniques.
Complete laboratory documentation in a timely and accurate manner.
Ensure compliance with SOPs, registered specifications, and cGMP standards.
Review batch paperwork and reconcile laboratory analyses, escalating out-of-specification (OOS) results per site procedures.
Assist in authoring and reviewing SOPs and other documentation.
Support technical transfer of new projects.
Participate in OOS investigations and deviations using the Infinity system.
Maintain chain of custody for samples using CIMS and LIMS systems.
Stay current with corporate, industry, and regulatory trends impacting QC and aseptic manufacturing.
Perform additional tasks as required by the Lab Supervisor.
Qualifications
A minimum of a third-level qualification (Degree) in Chemistry, Biology, or a related discipline.
2–5 years' experience in a pharmaceutical, healthcare laboratory, or related technical function.
Strong written and verbal communication skills.
Ability to work effectively in a team-based, collaborative environment.
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