QC Corner: When, Why and How to change vendors for QC testing solutions

Senior Technology and Market Dev Manager
Charles River Solutions
Marie France Quillen is the Senior Technology and Market Dev Manager for Charles River Solutions. With nearly two decades’ of experience in the life science industry,. Marie has a proven track record of driving results within pharmaceutical operations. Marie’s functional expertise includes QC, Lab testing, Engineering, Manufacturing and Quality Operations. Marie has extensive experience in aseptic production and successfully automating endotoxin testing programs within a GMP environment. She has also managed external manufacturing QA operations and compliance. She has worked with specialty API, vaccine products and insulin products and is skilled in compendia microbiological testing methods, analytical method transfer, sterility testing, growth promotion, method/development validation and equipment validation. During her tenure at Cardinal Health, Novo, Pfizer, Marie worked cross functionally across the organizations. Marie received her Bachelor of Science (BS) in Biological Sciences, and a Minor in Chemistry and Microbiology from the Metropolitan State University of Denver.

Learn why it is important and worth it to make a vendor change for QC testing solutions. In this video interview Marie France Quillen, from Charles River talks about the selection criteria process and best practices to make the required change. 

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Senior Technology and Market Dev Manager
Charles River Solutions
Marie France Quillen is the Senior Technology and Market Dev Manager for Charles River Solutions. With nearly two decades’ of experience in the life science industry,. Marie has a proven track record of driving results within pharmaceutical operations. Marie’s functional expertise includes QC, Lab testing, Engineering, Manufacturing and Quality Operations. Marie has extensive experience in aseptic production and successfully automating endotoxin testing programs within a GMP environment. She has also managed external manufacturing QA operations and compliance. She has worked with specialty API, vaccine products and insulin products and is skilled in compendia microbiological testing methods, analytical method transfer, sterility testing, growth promotion, method/development validation and equipment validation. During her tenure at Cardinal Health, Novo, Pfizer, Marie worked cross functionally across the organizations. Marie received her Bachelor of Science (BS) in Biological Sciences, and a Minor in Chemistry and Microbiology from the Metropolitan State University of Denver.