Responsibilities · Development and validation of LC-MS/MS methods for quantitation of drugs and biomarkers · Application of these methods to routine analysis of biological samples from pre-clinical toxicology, and clinical safety studies · Record keeping in compliance with GLP · Preparation of study plans and reports · You will play an active role in planning your work, managing your time to deliver data to our customers · Work closely as part of a team, supporting one another to achieve our customers goals The ideal candidate will; · Be enthusiastic, proactive, and driven to go the extra mile to support our customers · Focus on quality, and possess an excellent attention to detail · Communicate effectively; explaining the outcome of experiments to peers and customers Education, Skills & Experience · Degree in biological or analytical science, or equivalent relevant experience · Experience in a GXP accredited laboratory is advantageous · Knowledge of mass spectrometry and/or chromatography techniques