Scientific Associate

3 weeks ago

Tranent, United Kingdom Charles River Laboratories Full time

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.

**Job Summary**:
We are seeking an Assistant Scientist for our Veterinary Residues and Agrochemical Residues Group which is located at our site in Elphinstone, Tranent.

The following are responsibilities related to the Scientific Associate position:

- 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.

The following are minimum qualifications related to the Scientific Associate position:

- 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

**Profile and Requirements**:
**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 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

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