As an HPLC / LC-MS Laboratory Engineer, you will join a team of five scientists and report directly to the Technical Leader. Working with a remarkable diversity of samples, including small molecules, proteins, oligonucleotides, viral vectors, mRNA vaccines, peptides, formulation excipients and nanoparticles, you will play a direct role in generating the analytical evidence that supports the development of future medicines.
From early research activities through to clinical development and commercialisation, your expertise in liquid chromatography coupled with mass spectrometry will help ensure the quality, reliability and regulatory compliance of pharmaceutical products. Every analysis you perform contributes to bringing safe and effective therapies to patients faster.
now
- ing existing analytical methods to determine the identity, purity, and assay of various products in compliance with GMP requirements
- ing existing analytical in the context of bioanalytical studies in compliance with GLP (Good Laboratory Practice) and GcLP (Good Clinical Laboratory Practice) requirements
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Developing, validating, and adapting analytical protocols to meet specific project needs
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Performing analyses using state-of-the-art LC-MS instrumentation, including XevoTQ systems, QDa, and LC-SQD2
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Conducting stability studies and QC release testing
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Processing and interpreting analytical data
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Preparing analytical reports and related scientific documentation
