Job Description
Join a Growing GMP Analytical Team
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