Job 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
Skills, Education & Qualifications
- Degree in chemistry, biological or analytical science, or equivalent relevant experience
- Experience in a GXP accredited laboratory is advantageous
- Knowledge of mass spectrometry and/or chromatography techniques