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.
Key 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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