Lily Liu Shin
About Lily Liu Shin
Lily Liu Shin is a Senior Scientist and Global QC Raw Materials Lead at Kite Pharma, Inc., with extensive experience in analytical and formulation development within GMP and non-GMP environments. She has a strong background in biophysical and biochemical characterization of biologics, having held various roles at Agensys, Inc. over a span of more than a decade.
Work at Kite Pharma
Lily Liu Shin currently serves as the Senior Scientist and Global QC Raw Materials Lead at Kite Pharma, Inc. since 2018. In this role, she focuses on quality control processes related to raw materials, ensuring that they meet the necessary standards for therapeutic development. Her responsibilities include overseeing compliance and quality assurance in various projects, contributing to the overall success of Kite Pharma's operations in Santa Monica, California.
Experience at Agensys, Inc.
Lily Liu Shin has extensive experience at Agensys, Inc., where she held multiple positions from 2004 to 2015. She began her career there as a Quality Control Associate I in Analytical Development and progressed through various roles, including Biochemistry Associate I and II, Senior Biochemistry Associate, and Principal Associate in Analytical and Formulation Development. Her tenure at Agensys involved analytical method development, life cycle management, and setting up new QC/AD groups and labs.
Education and Expertise
Lily Liu Shin holds a Doctor of Philosophy in Molecular Biology, Biochemistry, and Philosophy from the University of Miami, Miller School of Medicine. She also earned a Master of Science in Biochemistry from the University of Saint Joseph and a Bachelor of Science in Biology and Chemistry from Emory University. Her educational background supports her expertise in GMP and non-GMP environments, particularly in the biophysical and biochemical characterization of biologics.
Background in Research
Lily Liu Shin began her research career as a Research Associate at Emory University School of Medicine, where she worked from 2000 to 2005. This role provided her with foundational experience in scientific research, which she later applied in her various positions within the pharmaceutical industry. Her background in research has been instrumental in her contributions to contract research and manufacturing organization activities.
Regulatory Compliance and Quality Assurance
In her current role and previous positions, Lily Liu Shin plays a key role in regulatory submissions, ensuring compliance and quality in therapeutic development projects. Her expertise in analytical method development and lifecycle management aids in maintaining high standards for product quality and regulatory adherence, which is critical in the biopharmaceutical industry.