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!!