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At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.
Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.
As a Charles River employee, you will be part of an industry-leading, customer-focused company at the forefront of drug development. Your skills will play a key role in bringing life-saving therapies to market faster through simpler, quicker, and more digitalized processes. Whether you are in lab operations, finance, IT, sales, or another area, when you work at Charles River, you will be the difference every day for patients across the globe.
Job Summary
We are currently recruiting for a Scientist who will be responsible for the planning and execution of projects to support in-house and contracted programmes of work performed within the MSAT team. The successful candidate will also be required to support wider processing activities within the MSAT team (upstream, downstream, analytics and molecular biology).
Profile and Requirements
Key duties and responsibilities include but aren't limited to:
1. Performing purification of plasmid DNA including Chromatography via AKTA and Tangential Flow Filtration.
2. Executing and completing Small-scale pre-production evaluations.
3. Assisting with Research grade production of plasmid DNA using kits up to giga prep scale.
4. Providing technical input into experimental design and troubleshooting.
5. Providing In-process analytics (productivity/purity) and data analysis.
6. Ensuring documentation is generated for protocols, study plans and study reports in a timely manner, and to a high standard as per Charles River policies, as assigned.
7. Supporting the development/continuous improvement of techniques/processes within the MSAT team and other areas of the business.
Qualifications and Key requirements:
1. A degree in Biology, Biotechnology, Biochemistry or equivalent scientific qualification.
2. Previous practical laboratory experience in Downstream Processing is essential.
3. Previous experience with basic laboratory techniques, including aseptic processing is essential.
4. The ability to demonstrate a strong understanding of cGMP manufacturing.
5. Able to demonstrate strong written and verbal communication skills.
6. The ability to work as part of a team and independently as required.
7. Be able to work under the pressure of client and business milestones and needs.
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 86% of the drugs approved by the FDA in 2021.
At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.
For more information, please visit www.criver.com.
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