Charles river laboratories memphis tn

Charles River Laboratories says it will expand its cell therapy facility in Memphis, Tennessee to enable clients to streamline and accelerate their programs. Contract development manufacturing organization CDMO Charles River will increase its existing 16 cleanrooms by adding nine charles river laboratories memphis tn suites at its Memphis plant. The company says that the facility expansion will support its cell therapy clients and help them to speed their programs to commercialization.

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. Please make sure work history and education are added correctly. The Manufacturing Science and Technology Intern is responsible for successfully completing the internship program course leading up to the potential involvement of various Analytical Science or Manufacturing Science related activities associated with the start-up of GMP production or QC lab activities of a number of novel cellular products. This includes compliance with regulatory agencies and associated guidelines. Must be able to meet physical requirements established in this job description.

Charles river laboratories memphis tn

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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. Each year more than 20, biologic testing reports are sent each and over licenses products are supported by our biologics testing solutions team. Experience with statistical analysis software preferred.

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Headquartered in Memphis, TN, Cognate produces various cell types and technologies used in cellular immunotherapy and immuno-oncology, regenerative medicine, and advanced cell therapy. Cognate specializes in cGMP cell therapy manufacturing, which processes a variety of cellular products and other starting materials to develop and produce allogeneic and autologous cell therapies. Cognate also offers cell therapy manufacturing solutions designed to be comprehensive, as well as solutions for the production of plasmid DNA and other CDMO value chain components. Privately-held Cognate was established in in Baltimore, and has since grown to more than employees, with operations in North America and Europe. Charles River reasons that in acquiring Cognate, it can provide its clients with an integrated solution from basic research and discovery through cGMP production, thus positioning itself as a premier scientific partner for cell and gene therapy development, testing, and manufacturing. That deal, completed on January 3, enabled Charles River to offer cell therapy developers and manufacturers a solution taking them from basic research through commercialization.

Charles river laboratories memphis tn

Manufacturing plant addition features nine new processing suites. Charles River Laboratories International, Inc. The expanded space is suitable for clinical and commercial cell therapy manufacturing, with an additional nine state-of-the-art processing suites, adding to an existing 16 cleanrooms. The suites use advanced cleanroom facility technology and are designed to be fully compliant with current good manufacturing practice GMP and international regulatory standards. They can accommodate flexible configurations to support client requirements, and are designed for high volume production, along with options for dual production lines for late stage clinical- and commercial manufacture. Read more about the expansion here. The partnership revolves around meeting various agency standards and industry requirements pertaining to the drug development and manufacturing lifecycle.

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When you join our family, you will have a significant impact on the health and well-being of people across the globe. With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. 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. Experience with design software preferred. 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. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. This includes compliance with regulatory agencies and associated guidelines. Display an ability to create and review cGMP documentation. 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. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. According to the firm, the suites will include advanced cleanroom facility technology and have been designed to meet GMP requirements.

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Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. For more information, please visit www. Charles River Laboratories is a visionary leader in the development and delivery of advanced drug therapies. Must possess effective written and oral communication skills. For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. 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. Perform other duties as assigned. The Manufacturing Science and Technology Intern is responsible for successfully completing the internship program course leading up to the potential involvement of various Analytical Science or Manufacturing Science related activities associated with the start-up of GMP production or QC lab activities of a number of novel cellular products. This includes compliance with regulatory agencies and associated guidelines. Display an ability to think critically and assess risk. Our dedicated employees are focused on providing clients with exactly what they need to improve and expedite the discovery, early-stage development and safe manufacture of new therapies for the patients who need them. The company says that the facility expansion will support its cell therapy clients and help them to speed their programs to commercialization. Charles River is an early-stage contract research organization CRO. According to the firm, the suites will include advanced cleanroom facility technology and have been designed to meet GMP requirements.