Analytical Chemist - GMP and Mass Spectrometry

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Posted 2 weeks ago
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About the role

An exciting opportunity has arisen for an experienced and technically skilled Analytical Chemist to join a specialist GMP laboratory supporting the development and analysis of advanced pharmaceutical products. This role offers the chance to work with cutting-edge analytical technologies while contributing to a rapidly expanding and highly collaborative scientific environment. The Opportunity As a key member of the analytical team, you will take a leading role in the development, validation, and optimisation of analytical methods for complex pharmaceutical matrices. You will serve as a technical expert in mass spectrometry and support the ongoing growth of analytical capabilities within a regulated GMP environment. Key Responsibilities Lead analytical method development, optimisation, and validation in line with ICH Q2(R2) guidelines Operate and develop methods using LC-MS/MS and GC-MS/MS platforms Utilise high-resolution mass spectrometry and ICP-MS for advanced analytical investigations Perform analysis using UHPLC, HPLC, and GC-based techniques Troubleshoot complex sample matrices, including lipid-based formulations and botanical extracts Support equipment qualification activities (IQ/OQ/PQ) and lifecycle management Contribute to computerised system validation (CSV) activities Act as a technical lead for mass spectrometry applications and capability development Support regulatory submissions, inspections, and audit readiness activities About You You will bring a strong background in analytical chemistry combined with hands-on GMP laboratory experience. Essential Requirements: MSc or PhD in Analytical Chemistry (or equivalent experience) Proven experience within a GMP-regulated laboratory environment Strong expertise in LC-MS/MS and GC-MS/MS method development Experience with ICP-MS analysis Knowledge of ICH Q2(R2), EU GMP, and ALCOA+ principles Experience using industry-standard chromatography and mass spectrometry software Desirable Experience: Pharmaceutical, cannabinoid, lipid, or botanical extract analysis High-resolution mass spectrometry Method transfer and lifecycle management activities Regulatory submission support

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