Join this thriving CRO as their next QC Officer Biologics.
They are looking for candidates with demonstrable cell and molecular-based experience.
This is a permanent role offering an attractive salary and a comprehensive benefits package, including many extras.
Responsibilities:
1. Oversee and manage routine batch release testing in the Biosafety and Cell Based Assay Department, including client correspondence, weekly calls, management of subcontractors, and ensuring samples are released within required timelines (scheduling tests, reviewing basic data, liaising with QA, generating CoA).
2. Generate and update GMP-compliant SOPs, protocols, and reports.
3. Source, purchase, and stock consumables, standards, and reagents required for testing.
4. Receive and process test samples in LIMS.
5. Perform data calculations, basic statistics, and trending. Provide additional information to clients as needed.
6. Assist in internal, regulatory, and client visits/audits, and respond to findings.
Minimum Requirements:
* At least 2 years of relevant experience in scientific research, preferably within a GMP-regulated environment (EMEA/FDA) in the pharmaceutical, medical device, or CRO industry.
* Project management experience is desirable.
* BSc/MSc in a relevant science discipline (e.g., cell biology, molecular biology, biomedical science).
* Experience in cell-based assays or molecular techniques is desirable but not essential.
Please note: Applicants must have a Stamp 4 visa or unrestricted full working rights for Ireland.
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