Josh York
About Josh York
Josh York serves as the Director of Operations at EyePoint Pharmaceuticals, bringing over twenty years of experience in cGMP and pharmaceutical manufacturing. His background includes significant roles at various companies, where he contributed to the development and production of dry powder formulations for inhalation.
Work at EyePoint Pharmaceuticals
Josh York has been serving as the Director of Operations at EyePoint Pharmaceuticals since 2021. In this role, he oversees various operational functions within the company, contributing to its strategic objectives. Prior to this position, he worked as the Operations Manager at EyePoint Pharmaceuticals from 2018 to 2021, where he managed operational processes and ensured compliance with industry standards. His extensive experience in pharmaceutical operations supports the company's mission to deliver innovative therapies.
Education and Expertise
Josh York holds a Bachelor of Science degree in Zoology/Animal Biology from New Mexico State University. His educational background provides a foundation for his extensive experience in the pharmaceutical industry. He has over twenty years of experience in current Good Manufacturing Practices (cGMP), focusing on the development and production of dry powder formulations for inhalation. His expertise includes creating and implementing standard operating procedures, master batch records, and protocols with an emphasis on quality and compliance.
Background in Pharmaceutical Manufacturing
Josh York has a diverse background in pharmaceutical manufacturing, having worked at several companies throughout his career. He began his career at Dura Pharmaceuticals Inc as a Manufacturing Associate from 1996 to 2001. He then worked at Control Delivery Systems as a Pharmaceutical Manufacturing/Development Associate from 2001 to 2004. Following that, he joined Millennium Pharmaceuticals as a Senior Research Associate in Formulations for eight months before moving to pSivida Corp, where he spent 13 years in operations focused on pharmaceutical manufacturing.
Key Contributions and Responsibilities
Throughout his career, Josh York has played a significant role in various operational initiatives. He was instrumental in the development, design, setup, and qualification of automated filling, packaging, and thermoforming lines. As a member of the Change Control Board, he was responsible for reviewing and approving controlled documentation, including standard operating procedures (SOPs), master batch records (MBRs), and validations. He also trained and supervised multi-departmental teams during the manufacture of developmental, clinical trial, and commercial products.