UCLA Health Los Angeles, CA, USA
Responsibilities Under the supervision of the Director of the Human Gene and Cell Therapy Facility (HGCTF), you will be responsible for the day-to-day Good Manufacturing Practices (GMP) quality assurance compliance activities including document control. Qualifications Bachelor of Science Degree or Master's degree in Biology, Chemistry, or related field and a minimum of one year of GMP quality assurance experience. Previous experience directly involved with federal regulations regarding GLP and GMP. Strong interpersonal communication skills to effectively and diplomatically interact with physicians, staff, administration & sponsors. Demonstrated skill in gathering pertinent data, preparing narrative reports, statistical reports, charts, graphs, and tables. Demonstrated ability to carry out analytical tasks, to identify and define issues and alternatives, to resolve problems, and to draw logical conclusions. Demonstrated skill in reviewing data and material...
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