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maintenance. Develop and implement process control plans, including equipment qualification and process change control. Enter patient/product information into databases, generate reports, and ensure meticulous
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operation of mechanical systems, monitoring systems, and equipment. Coordinate preventative maintenance and maintain cGMP compliance for building systems and major process equipment. Conduct internal cGMP and
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Associate II (QCA II) to support in-process and release testing for GMP Manufacturing and analytical development of gene and cellular immunotherapy products. This fast-paced lab engages in cutting-edge
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Associate III (QCA III) to support in-process and release testing for GMP Manufacturing and gene and cellular immunotherapy products. This fast-paced lab uses cutting-edge technology for clinical
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techniques. · Receives, distributes and maintains supply inventories in laboratories as needed · Prepares simple stains, solutions, culture media, and may process tissue following established
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metabolic alterations in this process. They are also interested in characterizing the role of health disparities on these mechanisms. For more information about Dr. Shuck’s lab, please visit here. As a
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to appropriate committees, ensuring timely completion of the approval process. Keep stakeholders informed of protocol approval and activation issues, including regulatory status updates for sponsors and
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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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accurate documentation throughout the research process. Compile and submit data according to protocol guidelines, ensuring compliance with study requirements. Actively recruit patients for studies and assist
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, shaping the future of medicine through cutting-edge research. The QC team for Cellular and Gene Therapy Operations seeks a skilled Quality Control Manager to oversee in-process and release testing for GMP