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
Ideal Candidate
* 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
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