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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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, 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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participation in professional organizations, scientific conferences, reading industry journals, and publication of manuscripts. Basic education, experience and skills required for consideration: PhD in applied
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close collaboration with other team members and external partners from academia and industry. Train and supervise technical staff. Your qualifications should include: Recent PhD in the field of either
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. · Cooperates with other performance improvement and compliance activities within the department and in the institution. · Maintains current knowledge of analytical techniques and industry practices
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as Manufacturing, Quality Control, and Quality Assurance staff. You will also assist with regulatory maintenance, amendments/approvals (IRB, IBC, and IACUC), training documentation, etc. to ensure regulatory
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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
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characterization of tumors from extensive multi-omics datasets, • Collaborate with fellow researchers from both academic and industry sectors, • Provide training to other lab members, • Publish
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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