Pat Jones is a Medical Laboratory Technologist with more than 40 years of experience in the health-care and pharmaceutical/biologics manufacturing and consulting industries, including over 25 years in Quality and Compliance.
She is currently employed at Therapeutic Products, Inc. (TPIreg), as the Director, Quality and Regulatory Compliance. Pat worked at CanReg, Inc. (now known as OptumInsight), from 1999 to 2008, most recently as Associate Director, Compliance, Clinical Services, then from 2008 to early 2014, as an independent Quality and Compliance consultant.
Pat’s primary focus is compliance auditing, training, and project management in the areas of GLP, GCP, GMP, ISO (medical devices) and related Quality Systems.
Pat is a member of the Regulatory Affairs Professionals Society (RAPS), and holds certifications in Canadian, US, and European Regulatory Affairs. Pat is Past President of the Canadian Chapter of the Association of Clinical Research Professionals (ACRP), past Member of the ACRP Global Membership Committee and a current Member of the Global Professional Development Committee. She is a member of the Clinical Research Association of Canada (CRAC), and the Canadian Association of Professionals in Regulatory Affairs (CAPRA). Pat is a regular speaker at meetings and conferences for ACRP, other professional organizations, and health-care companies and institutions.