Chris Oswald

Chris has more than 20 years of Good Manufacturing Practice (GMP) pharmaceutical experience, with a background as a manufacturing manager in the pharmaceutical contract manufacturing (CMO) industry. He has experienced the realities of balancing revenue delivery with quality, while navigating the challenges of shepherding products through the molecular development process. Chris has a wide range of experience from being a corporate quality and regulatory representative to plant manager for Agilent Technologies. Chris has led many operational aspects including quality systems engineering, personnel and staffing proposals, shift structures, cost of goods estimations, return on investment, equipment evaluation and DQ, as well as the countless CMC items that are necessary to help push product(s) through to commercialization. Chris graduated from Colorado State University with a BS in Biology and a BS in Zoology with minors in Chemistry and Biochemistry.