Chad Glyde

Chad Glyde

Director Of Quality @ Noveome Biotherapeutics

About Chad Glyde

Chad Glyde serves as the Director of Quality at Noveome Biotherapeutics, Inc., where he has worked since 2018. He possesses a strong analytical background and extensive experience in quality control within the pharmaceutical industry.

Work at Noveome Biotherapeutics

Chad Glyde has been with Noveome Biotherapeutics, Inc. since 2016. He initially served as Associate Director of Quality Control from 2016 to 2018, where he contributed to quality assurance processes. In 2018, he advanced to the position of Director of Quality, a role he has held for six years. In this capacity, he oversees quality systems for both clinical-stage and commercial products, ensuring compliance with regulatory standards.

Previous Experience at Hospira

Prior to his tenure at Noveome Biotherapeutics, Chad Glyde worked at Hospira as a Quality Engineer in Marketed Product Quality from 2014 to 2015. His role involved maintaining quality standards and addressing product-related issues, contributing to the overall quality management system.

Background at Boehringer Ingelheim

Chad Glyde's career includes significant experience at Boehringer Ingelheim, where he held multiple positions. He started as a Chemist II from 2005 to 2010, then became Stability Coordinator from 2010 to 2012, and later served as Stability Program Supervisor - Quality Control from 2012 to 2014. His roles involved managing stability programs and ensuring quality control in pharmaceutical products.

Education and Expertise

Chad Glyde earned a Bachelor's degree in Chemistry from Ohio University, completing his studies from 1999 to 2004. His educational background, combined with his extensive laboratory and analytical experience, has equipped him with the skills necessary to identify and solve complex problems in a cGMP environment.

Achievements in Quality Management

Throughout his career, Chad Glyde has implemented and overseen quality systems for both clinical-stage and commercial pharmaceutical products. His expertise in managing stability programs and his leadership in quality control have contributed to the integrity and compliance of the products he oversees.

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