Role Overview & Mandate
Executive Summary
For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug...
Reviewed by Compensation & Visa Analysts •
Sources: USCIS E-Verify & Home Office CoS
For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.
IMPORTANT: In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please make sure work history and education are added correctly.
Job Summary
The primary function of Chromatographic Bioanalysis is to perform quantitative analysis of drugs and/or metabolites in biological samples, usually fluids such as plasma and serum. These samples arise from both preclinical and clinical studies aimed at providing data for the development and registration of pharmaceuticals.
The main duties of this position will involve the validation and application of analytical methods to quantify the levels of drugs and metabolites in biological fluids. As an Assistant Scientist you will be fully trained in all aspects of these studies, including sample processing, set-up/operation of analytical systems, primarily HPLC with mass spectrometric detection (LC-MS), and data review and processing (using Watson Laboratory Information Management System), so that you can play a full role in the conduct of bioanalytical studies.
A working knowledge of sample preparation and chromatographic techniques, including HPLC and/or LC-MS, would be a distinct advantage, though not essential as full training will be given.
- Use HPLC with MS detection for quantification of compounds in liquid matrices
- Carry out experiments in support of method validation and subsequent routine samples generated within GLP Voluntary and GLP regulatory studies
- Required to follow written instructions (SOPs, protocols, analytical procedures) and document details of steps carried out to ensure compliance through recreation of events
- Performing technical laboratory activities in support of client studies or procedures
- Performing analysis of data for quality and completeness and determines if results are as expected.
- Recording data in compliance with company and regulatory policies and standards to meet quality and accuracy requirements.
- A BSc in a Chemistry or related discipline
- A working knowledge of sample preparation and chromatographic techniques
- Good problem solving skills and be able to work to tight deadlines and record data accurately
- The ability to communicate effectively
The starting salary for this position is £24,876.69. Successful candidates will be appointed to the bottom of the pay band if they have no relevant experience. In exceptional circumstances where the candidate has relevant equivalent experience, this will be taken into consideration.
The closing date for applications is 21 February 2023.
Profile and Requirements
IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.
About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.
