QC Analyst

About

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