QC Analyst – Ireland
Contract - PAYE
Location On site - Ireland
Atrium (EMEA) are supporting a global biopharma company we are looking for a detail-driven QC Analyst to join a leading pharmaceutical organisation. This is an exciting opportunity to play a key role in ensuring the quality, safety, and compliance of pharmaceutical products through laboratory testing and analytical excellence.
Key Responsibilities
Perform routine and non-routine testing of raw materials, in-process samples, and finished products and Conduct analytical testing using techniques such as: HPLC, GC, UV/Vis spectroscopy, and dissolution testing
Accurately record and review test results within laboratory systems (e.g. LIMS)
Ensure compliance with GMP / GLP standards, SOPs and regulatory requirements and Verify data for accuracy, integrity, and completeness
Support out-of-specification (OOS) and deviation investigations Troubleshoot analytical issues and equipment failures.
Assist in root cause analysis and implementation of corrective actions
Perform routine calibration and maintenance of laboratory equipment
Ensure the laboratory remains audit-ready at all times
Support method development, validation, and transfer activities
Contribute to continuous improvement initiatives within QC
What We’re Looking For
Degree in Chemistry, Pharmaceutical Science, or Engineer
Experience working in a GMP-regulated laboratory (preferred)
Hands-on experience with analytical techniques (HPLC, GC, etc.)
Strong attention to detail and problem-solving skills
Ability to work both independently and collaboratively
Why Apply
Be part of a high-performing Quality team in a regulated industry
Gain exposure to advanced analytical techniques and systems
Opportunity to contribute to critical quality and patient safety outcomes
Work in a supportive, collaborative environment
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