QC Analyst

Job Description Tittle: QC Analyst Location: Dublin, Ireland Contract Duration: 6-month contract Rate: 19.72 Hourly Looking to take the next step in your QC career? Join a leading biopharmaceutical company and support release and stability testing within a GMP-regulated QC laboratory environment. Responsibilities will include (but not limited to): Perform release and stability testing of drug substance and drug product samples Review and analyse laboratory data Document testing activities in line with GMP and Data Integrity requirements Support OOS, OOT, deviation investigations, and CAPA activities Assist with method transfers, validations, and stability studies Support audit readiness and continuous improvement initiatives Must Have: BSc degree in Biochemistry, Biotechnology, Pharmaceutical Science, Chemistry, Microbiology, or a related Life Sciences discipline. 2-4 years' experience in a GMP-regulated pharmaceutical or biopharmaceutical QC laboratory. Hands-on experience performing HPLC and/or UPLC testing for release, stability, or in-process samples. Experience using Empower or similar chromatography data systems for data acquisition and review. Strong understanding of cGMP, GDP, ALCOA+, and Data Integrity requirements. Experience reviewing analytical data and identifying atypical, OOS, OOT, or deviation events. Experience authoring or reviewing laboratory documentation such as SOPs, protocols, test methods, and reports. Ability to work independently while managing multiple priorities in a fast-paced QC environment. Biologics or biopharmaceutical QC testing experience. Experience supporting method transfers, method validation, or co-validation activities. Experience supporting audits, inspections, or inspection readiness activities. Exposure to stability programs and drug substance/drug product release testing. We're actively shortlisting, apply now or get in touch today to avoid missing out!!