Joe has 19 years of experience working in in the pharmaceutical and biotechnology industries with focuses on cellular therapy, plasma purification, monoclonal antibody production, and medical devices within research and development and GMP QC functions. He possesses a background in method development and validation, equipment qualification, lean laboratory management, and commercial testing across multiple types of product streams. His past experience includes greenfield startup of a plasma fractionation testing lab, streamlining sample workflows and testing to improve efficiency and reduce costs, and end to end management of QC testing from incoming raw material receipt to environmental monitoring and drug product release to support GMP operations.
Joseph Dwyer
