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
Contact Detail:
Resolian UK Recruiting Team