Ken Miller

Dr. Miller is a Director in Global Quality at BioMarin and leads a team that is responsible for the design, implementation and harmonization of stability programs for clinical and commercial products within BioMarin’s portfolio. His team is also responsible for the management of CMC analytical data packages that are included in regulatory submissions and annual product reviews. Dr. Miller holds a Bachelor of Science degree in Biochemistry from Case Western Reserve University and a Doctor of Philosophy in Biological Sciences from Carnegie Mellon University. Prior to joining BioMarin, Dr. Miller served in leadership positions for 18 years within analytical functions at MedImmune Biopharmaceutical Development and AstraZeneca Biologics Global Technical Operations. Besides his role at BioMarin, Dr. Miller is also currently an adjunct faculty member at UMBC, where he teaches “Quality Control and Quality Assurance of Biotechnology Products” for a Master’s of Professional Studies in Biotechnology program.