Shannon Christensen is an experienced professional in quality management systems and documentation control within the pharmaceutical and engineering sectors. Currently serving as a Consultant QMS at Kronos Bio, Inc. since June 2021, Shannon has previously held roles such as Associate Director of QA Document Control at Intarcia Therapeutics, Inc., and Documentation Specialist/Project Coordinator at Genentech, where responsibilities included the management of documentation in both electronic and printed formats. Earlier experience includes serving as a Documentation Specialist at Transnuclear Inc., where work involved managing documentation for design engineering projects. Shannon holds a Certificate in Regulatory Affairs from UCSC Silicon Valley Extension obtained in 2012.
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