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