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Genentech, Biotechnology Company, Modernizes Global Drug Safety Submissions Records Management System

Updated: Mar 4




Genentech – Biotechnology

Technical Product Manager – Contract - South San Francisco, CA | Dec. 2007 – Apr. 2008

Technologies: LiveLink Enterprise Document Management and Vignette Portal


In my role as a Sr. Enterprise Content Management expert, I led an effort to define and document requirements for complex Quality Assurance Controlled Documents creation, management, change control, and historic traceability for the enterprise.


I co-created and authored business processes, business requirements, functional, technical, and document taxonomy requirements for this regulated Document Management (DM) system to manage documents being used for the highly regulatory drug safety submission process.


The project included defining a method and process to inventory, migrate, and retire the legacy Quality Assurance Document Control system and workflows migrate 1 million documents into the new DM. 

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