Benjamin Z.

Benjamin Z. has extensive experience in quality control and analytical processes within the biotechnology and pharmaceutical industries. Currently a Senior Quality Control Specialist at Novo Nordisk since April 2020, responsibilities include the deployment of iStability software for lot release and stability data analysis, alongside FDA regulatory filing support. Previous roles include Senior Quality Control Associate at both Lundbeck and Alder Biopharmaceuticals, where project management and data verification for GMP validation were key tasks. Career beginnings involved analytical method development at SNBL USA and research roles in various organizations, focusing on both quality assurance and research initiatives. Benjamin Z. holds a Bachelor of Science in Chemistry from Seattle University.