Description Responsibilities You will be responsible for development and validation of quantitative LC/MS/MS methods for the analysis of drugs and metabolites in biological matrices Application of these methods to routine analysis of samples from pre-clinical and clinical studies Record-keeping in compliance with GLP/GCP Preparation of study plans and reports Education, Skills & Qualifications Studying towards a Degree in chemistry or related subject Experience of chromatographic techniques i.e. HPLC, LC/MS and ability to problem solve Good written and verbal communication skills Computer literate Ability to work with minimum supervision and as part of a team Conscientious and meticulous in laboratory work Excellent time management skills and ability to work to tight deadlines Highly motivated Willing to get involved with new ideas and initiatives Experience in working in an analytical chemistry laboratory Familiarity with quantitative LC/MS/MS analysis We offer a flexible approach to work, in a friendly and informal environment. As well as a competitive salary, we offer a range of flexible benefits including a group personal pension plan, cycle to work scheme, private health service and many more.