Job Summary:
We are currently recruiting for a QC Analyst to join a busy Quality Control laboratory in Dublin on an initial 12 month contract. This is a hands-on analytical role supporting raw material, in-process, finished product, and stability testing. The successful candidate will ensure all laboratory testing and data review activities are completed on time and in full compliance with GMP, GLP, and regulatory requirements, directly supporting production and product release schedules.
Responsibilities:
- Perform analytical testing on raw materials, intermediates, finished products, and stability samples, ensuring all testing is completed within required timelines and in compliance with GMP and GLP standards
- Support production and shipping schedules through timely and accurate testing and data review
- Peer review analytical data and laboratory documentation
- Report Out of Specification (OOS), Out of Trend (OOT), and atypical results in line with approved SOPs
- Support method troubleshooting, investigations, and continuous improvement initiatives
- Update and maintain QC test methods, procedures, and associated documentation as required
- Drive Right First Time (RFT) performance and contribute to achieving laboratory KPIs
- Perform all laboratory activities in accordance with GMP, GLP, and applicable regulatory requirements, including EU MDD 93/42/EEC and EN ISO 13485
- Maintain a strong safety, quality, and compliance culture within the QC laboratory
- Ensure high standards of housekeeping and 6S are consistently maintained
- Ensure correct use, care, and maintenance of laboratory equipment and support preventive maintenance activities
- Demonstrate competency in analytical techniques and laboratory systems such as LIMS, LabX, and UV software
- Participate in all required training, assessments, and SOP reviews
Requirements:
- Degree or equivalent qualification in Chemistry, Pharmaceutical Science, or a related scientific discipline
- Experience working in a GMP/GLP-regulated QC laboratory environment
- Strong knowledge of analytical techniques and laboratory systems (e.g. LIMS, LabX, UV software)
- Experience with raw material, finished product, and/or stability testing
- High attention to detail with strong documentation and data review skills
- Proactive, collaborative mindset with a commitment to continuous improvement
- Strong understanding of quality, compliance, and safety standards
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