Madelyn Yost

Madelyn Yost, MBS, currently serves as Associate Manager in Regulatory Affairs at Ferring Pharmaceuticals, where responsibilities include the preparation, coordination, execution, and ongoing maintenance of CMC regulatory submissions, as well as the preparation of CMC sections for various reports. Prior to this role, Madelyn worked at Legend Biotech as a Quality Control Analyst, focusing on the creation and approval of QC documents and performing QC testing for CAR-T product manufacturing in a cGMP cleanroom environment. Earlier experience includes serving as a Quality Control Laboratory Technician at Roche Molecular Systems, where analysis of compounds and maintenance of databases were key responsibilities. Madelyn holds a Master’s Degree in Biological and Biomedical Sciences from Rowan University and a Bachelor of Science in Public Health and Biology from Rutgers University.