KP Charpentier
Manager, Quality Systems, Trilink Biotechnologies 

Quality compliance professional with expertise in US/EU cGMP manufacture of sterile injectables as well as ISO 9001:2015 quality systems requirements. Background includes 11 years as a quality control microbiologist supporting sterility assurance testing and environmental monitoring activities – a role in which I was also responsible for leadership of the lab – as well as 6+ years in quality compliance roles with a focus on auditing, including conducting supplier audits and internal audits, as well as managing and hosting customer audits and ISO certification audits for a contract manufacturing biotechnology firm.