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innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research. A Cell Manufacturing Associate (Level 1 or Level 2 depending on education and
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compliance with all Federal and State laws and regulations and other accrediting agency requirements in the collection, processing, preparation, and distribution of biopharmaceutical products manufactured in
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, preventing, and curing diseases, shaping the future of medicine through cutting-edge research. Responsible for manufacturing and isolating of human islets from pancreas donors under limited supervision
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-process and release testing of GMP Manufacturing and analytical development for cellular immunotherapy products. This is a fast-paced lab involved in cutting edge technology, research and clinical cellular
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Manufacturing and analytical development of cellular immunotherapy products. As a successful candidate, you will: · Manage QC staff and oversee in-process and release testing for GMP Manufacturing
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Summary: Coordinates and develops coverage analyses and budgets for both industry sponsored and non-industry sponsored clinical trials, along with any corresponding amendments. Liaises between external
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. They will be responsible for completion and management of regulatory documents for industry and other sponsors, such as, FDA Form 1572, financial disclosures, protocol cover pages, and other documents
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collaboration with other team members and external partners from academia and industry, including presentation of progress internally or externally · Train and supervise technical staff Your qualifications
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cryopreserve cell cultures (e.g., T cell and tumor cell lines). · Assist in developing and adapting new manufacturing procedures and analytical methodology. · Assist in creating, reviewing and
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edge technology, research and clinical immunotherapeutic programs. New personnel will be trained in project specific techniques and procedures. As a successful candidate, you will: · Manufacture