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, charles river laboratories memphis tn. Contract development manufacturing organization CDMO Charles River will increase its existing 16 cleanrooms by adding nine processing 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.

Charles river laboratories memphis tn

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Each year more than 20, biologic testing reports are sent each and over licenses products are supported by our biologics testing solutions team. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

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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.

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. Properly supporting market access for a newly launched product with a single indication is challenging.

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Must be able to meet physical requirements established in this job description. Must be detailed oriented and have excellent organizational skills. Must possess effective written and oral communication skills. Furthermore, the CDMO claims that the suites will be able to accommodate flexible configurations, high volume manufacturing, and the option for dual product lines for late stage and commercial production. 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. 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. The company says that the facility expansion will support its cell therapy clients and help them to speed their programs to commercialization. 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. According to the firm, the suites will include advanced cleanroom facility technology and have been designed to meet GMP requirements. Contract development manufacturing organization CDMO Charles River will increase its existing 16 cleanrooms by adding nine processing suites at its Memphis plant. All signs point towards this rapid growth continuing in the coming years. 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. Display an ability to create and review cGMP documentation.

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Charles River Laboratories is a visionary leader in the development and delivery of advanced drug therapies. Additionally, the suites have dedicated air handling to avoid cross-contamination, as well as templated two-dimensional modular construction to aid the flow of materials and reduce risk to the product. Must be able to meet physical requirements established in this job description. All signs point towards this rapid growth continuing in the coming years. For more information, please visit www. Display an ability to create and review cGMP documentation. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. Perform other duties as assigned. This includes compliance with regulatory agencies and associated guidelines.