QC Batch Release Coordinator Location: West of Ireland Type: Permanent role
Join this thriving CRO as their next QC Officer Biologics.
They are looking for candidates with demonstrable cell and molecular-based experience.
Benefits include an attractive salary and a full suite of comprehensive benefits, with many extras included.
Responsibilities: Oversee and manage routine batch release testing in the Biosafety and Cell-Based Assay Department, including client correspondence, weekly calls, management of subcontractors, ensuring samples are released within required timelines (scheduling tests, reviewing basic data, liaising with QA, generating CoA, etc.
). Generate and update GMP-compliant SOPs, protocols, and reports. Source, purchase, and stock consumables, standards, and reagents required for testing. Receive and process test samples in LIMS. Perform data calculations, basic statistics, and trending analyses.
Provide additional information to clients as required. Assist in internal, regulatory, and client visits/audits and respond to findings. Minimum Requirements: A minimum of 2 years 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 and molecular techniques is desirable but not essential. Applicants must have a Stamp 4 or unrestricted full working rights for Ireland. Application: Reach out to ******
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