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
Job ID: 490917044
Originally Posted on: 8/27/2025
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