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