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Client:
Location:
Tranent, United Kingdom
Job Category:
Other
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EU work permit required:
Yes
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Job Reference:
242324d7f041
Job Views:
7
Posted:
14.07.2025
Expiry Date:
28.08.2025
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Job Description:
For 70 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 anAssistant Technician 1for ourFormulation Services Departmentlocated inElphinstone, Tranent.
Working as an Assistant Technician 1 you’ll join a team responsible for the storage and control of test items and the preparation of formulations supporting toxicology studies.
Duties and responsibilities include:
* Lab preparation and housekeeping
* Stock control, ordering, organisation and replenishment
* Calibration and maintenance of routine lab equipment
* Preparation of Vehicles, general reagents used to prepare formulations
* Disposals
* Delivery of Formulations
* Taking archive samples, test item weighings
Applicants should have:
* At least 3 NAT5s including Maths, English
What you can expect from us:
* A clear career progression
* A structured Training programme
* Access to private medical cover and employee assistance programme
* Employee discount scheme – discounts across hundreds of retailers!
* Paid opportunity to volunteer for 12.5 hours each year
* Free onsite fitness suite and fitness lessons
* Staff canteen
* Free onsite parking
The salary for this position is £23,842.35 per annum. In exceptional circumstances where the candidate has relevant equivalent experience, this will be taken into consideration.
The closing date for applications is Wednesday, 16 July 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 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.
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 Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 17,000 employees within 90 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2019, revenue increased to $2.62 billion.
At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of ~85% of the drugs approved by the FDA in 2019.
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