Ambitious, results-oriented, enthusiastic quality and compliance professional with more than 30 years experience in a regulated industry, combining healthcare and pharmaceutical experiences. Dynamic leader and team builder, motivating others toward success. Certifications as Quality Auditor (ASQ) and Program Manager (University of Penn) with a unique background as a Job Coach, College professor, Clinical Lab Manager, and Quality Auditor. Subject matter expert in regulatory compliance for the development of cell based products in pharmaceutical industry. Responsible for leading the deployment of cell therapy regulations into J&J’s supply chain. Current responsibilities are the deployment and maintenance of the R&D compliance program for GMP aspects within J&J’s Pharmaceutical Sector, which includes the development of the quality and compliance strategies to support new platforms that are in-licensed or developed within the Pharmaceutical Sector.
Director Commercial Apheresis Operations at The Janssen Pharmaceutical Companies of Johnson & Johnson
Master of Science (MS), Organizational Design