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 rele...