Cody Beaumont
Associate Director Quality Compliant and Regulatory, CAI
Experienced quality professional with expertise in the quality, analytical method development, formulation, clinical research, and characterization of material properties. I have extensive experience in clinical and commercial manufacturing drug substance, drug product, and API as well as coordinating CMO and CDMO activities related to manufacturing and quality processes. A large part of my career has been dedicated to developing high functioning and efficient teams focused on GMP/GLP QA/QC, and research. I have a passion for developing and organizing efficient fit for purpose processes. I have a deep understanding of GMP/GLP compliant practices in manufacturing and clinical research. I am adept at management and leadership and highly dedicated to staff growth through career development. I have a great deal of experience in coordination and overseeing phase specific and commercial activities related to CMO/CDMO for process and technical transfers from upstream development through complete fill/finish.
