Nancy Mize has extensive experience in quality assurance and compliance within the pharmaceutical industry, currently serving as the QA Documentation Lead at Gilead Sciences since June 2013. Prior roles include QA Documentation Specialist II at Gilead, Manager of Compliance at Roche Palo Alto from July 2002 to March 2010, Sr. Compliance Analyst at Roche Bioscience from November 1998 to July 2002, and Business Project Coordinator at Roche from July 1995 to November 1998. Mize began her career as a Supervisor in Administrative roles at Syntex from September 1974 to July 1995. Educationally, Mize holds a Business Management Certificate from Cañada College.
This person is not in any teams
This person is not in any offices