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...
Employment Type (feed only): |
FULL TIME
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