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development and quality control (QC) activities to ensure GMP compliance for CBM products. Recruit, manage, and train QC staff for tasks in a cGMP facility. Review, revise, and develop standard operating
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experience or combined education and experience in related field. City of Hope is an equal opportunity employer. To learn more about our commitment to diversity, equity, and inclusion, please click here
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and graphical representations. Develop specialized skills in relevant laboratory research areas to support ongoing projects. Ensure strict compliance with safety protocols in material handling, storage
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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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facility following SOPs. Develop and perform assays for product release (e.g., viral vectors, plasmid DNA, recombinant proteins). Maintain inventory, lab support, and equipment maintenance, including quality
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and procedures regarding conducting multiple clinical research trials. Develop and maintain knowledge of institutional protocol submission procedures and requirements. Manage multiple medium to high
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, plasmid DNA, and recombinant proteins. Maintain accurate inventory, support routine lab activities, and handle data entry and reporting. Develop and adapt analytical methodologies, process control plans