QC Material Management Analyst – Dublin

We are partnering with our Client, a leading global biopharmaceutical company, to hire a QC Material Management Analyst at their state-of-the-art Multi-Product Cell Culture Drug Substance facility in Dublin. This is a fantastic opportunity to be part of a high-performing QC Site Operations team in a GMP-regulated environment.

Key Responsibilities:

• Manage and process samples (Drug Substance, Drug Product, Raw Materials) in collaboration with Manufacturing, Engineering Stores, and Cryogenics Logistics.

• Log and release samples using LIMS/CIMS; store and reconcile backup/reserve samples.

• Perform QC testing (e.g., TOC, Nitrates, Conductivity) and analysis using HPLC, KF, UV, IR, and wet chemistry techniques.

• Ensure compliance with SOPs and GMP standards; assist in document authorship and batch reviews.

Requirements:

• Degree in Chemistry, Biology, or a related scientific discipline.

• Minimum 1 year of experience in a pharmaceutical, healthcare, or technical lab setting.

• Strong communication skills and a collaborative, detail-oriented mindset.

Ready to advance your career with a company that's transforming patients’ lives through science? Apply now or contact us to learn more.