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A leading contract research organization seeks a Scientific Associate in Tranent. In this role, you will perform analyses using HPLC and ensure compliance in laboratory studies. The ideal candidate holds a BSc in Chemistry and has experience with chromatographic techniques. This position offers a competitive salary of £27,163.48 annually and various benefits, including health care and employee discounts.
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Tranent, United Kingdom
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12.08.2025
26.09.2025
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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.
We are seeking an experienced Scientific Associate for our Safety Assessment Group located in Elphinstone, Tranent. This position is a 12-month fixed-term contract.
The following are responsibilities related to the Scientific Associate position:
The following are minimum qualifications related to the Scientific Associate position:
What you can expect from us:
Salary for this role is £27,163.48 per annum. The closing date for applications is 18 August 2025.
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 experienced team designs and executes programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Approximately 300 IND programs are conducted annually in our Safety Assessment facilities.
About Charles River: Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both GLP and non-GLP, supporting clients from target identification through preclinical development. We also provide products and services for clinical laboratory testing and manufacturing. This broad portfolio allows clients to create a flexible drug development model, reducing costs and increasing speed to market.
With over 20,000 employees across 110 facilities in over 20 countries, we are positioned to coordinate worldwide resources and apply multidisciplinary perspectives to resolve client challenges. Our client base includes global pharmaceutical and biotech companies, government agencies, hospitals, and academic institutions worldwide.
At Charles River, we are passionate about our role in improving lives. Our mission, science, and purpose guide us daily, and our work helps improve health and well-being globally. We have contributed to 80% of drugs approved by the FDA in the past five years.
We value diversity and inclusion and actively recruit talent from all backgrounds.