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Russell Tobin collaborates with a prominent global biologics manufacturer, known for its dedication to enhancing the well-being of patients and staff. They hold the prestigious title of being one of Ireland's top large workplaces, and their commitment to impactful change is evident in their daily actions.
Currently, they are in search of a QC Material Management Analyst who is responsible for supporting site activities related to Sample Management Laboratory, in-process samples, and laboratory duties in accordance with cGMP regulations.
Qualifications & Experience
* Degree in Chemistry/Biology or related discipline along with at least 1 year of experience in a pharmaceutical / healthcare laboratory or related technical function.
* Coordinate with departments to ensure timely sample processing and delivery.
* Manage sample receipt, logging, labelling, storage, and release for QC testing.
* Perform QC tests (e.g. HPLC, KF, UV, IR, wet chemistry) and document results accurately.
* Support SOP/document creation, batch record review, and GMP compliance.
* Collaborate effectively, communicate clearly, and handle additional lab duties as needed.
What’s on offer:
* A diverse team and a culture of no blame. Every mistake is a learning opportunity.
* Work with a company and co-workers who truly value the difference that they make.
* Excellent work/life balance and onsite benefits including gym, parking and many sports clubs.
Interested?
Please click on APPLY today!
Seniority level
* Seniority level
Associate
Employment type
* Employment type
Contract
Job function
* Job function
Quality Assurance
* Industries
Pharmaceutical Manufacturing
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