Joyce Bloomfield Merck Sharp & Dohme Corporation

Ms. Bloomfield has been with Merck Sharp & Dohme Corp. since 2008 in the Merck Manufacturing Division. She has held multiple positions in the pharmaceutical industry responsible for providing strategic direction in Global GMP Systems and Compliance, Quality Operations and Quality Management Systems. She was previously head of External Manufacturing Quality Assurance and Quality Management Systems at Merck. She directed the development and implementation of a new harmonized Quality Management System after the Schering Plough and Merck merger. Most recently, she has responsibility for several divisional Quality Assurance groups including Quality Management Systems, Global Regulatory Surveillance, Auditing, Labeling, Stability, Computer and Process Validation where she has oversight of global quality and compliance standards. She has more than 22 years combined pharmaceuticelal, consulting, and regulatory expertise where she provided strategic and technical solutions to senior management on complex regulatory, compliance and cGMP issues for pharmaceutical, medical device and biologic companies. Ms. Bloomfield has held executive roles in Cardinal Health's Pharmaceutical & Technology Services, and Corporate Quality Compliance Branch, was a Senior Consultant with KMI/PAREXEL Consulting, a Compliance Officer in CDER's Division of Manufacturing and Product Quality, and a Parenteral Drug Investigator with FDA's ORA. She holds a B.A. degree from Murray State University and is a certified Medical Technologist of the American Society of Clinical Pathology.