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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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. · 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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-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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for Gene Therapy. You will join a well-established group performing cutting-edge research, development and qualification of large-scale processes, and manufacture of products for gene therapy clinical trials
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, determine substitute material availability, communicate risks or concerns to supply, manage open orders and requests Consult with Purchasing, Sourcing, Manufacturing/Quality Control and Vendors, as required
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close collaboration with other team members and external partners from academia and industry. Train and supervise technical staff.
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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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. Review and provide feedback on monitoring findings to ensure compliance. Prioritize urgent requests from multiple sites and communicate issues to the Director. Serve as liaison between drug manufacturers
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analytics within industry or academic environment, developing and successfully implementing statistical and machine learning models for data mining, classification, prediction and clustering
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, determine substitute material availability, communicate risks or concerns to supply, manage open orders and requests Consult with Purchasing, Sourcing, Manufacturing/Quality Control and Vendors, as required