Job Opportunity: QC Officer Biologics at a Thriving CRO
Join this dynamic Contract Research Organization as their next QC Officer Biologics. This is a permanent position offering an attractive salary and a comprehensive benefits package, including many additional perks.
Responsibilities:
1. Oversee and manage routine batch release testing in the Biosafety and Cell-Based Assay Department. This includes client correspondence, weekly calls, managing subcontractors, ensuring timely sample releases, scheduling tests, reviewing data, liaising with QA, and generating Certificates of Analysis (CoA).
2. Generate and update GMP-compliant SOPs, protocols, and reports.
3. Sourcing, purchasing, and stocking consumables, standards, and reagents required for testing.
4. Receipt and processing of test samples in LIMS.
5. Perform data calculations, basic statistics, and trending analyses. Provide additional information to clients as required.
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 with 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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