A globally recognized Author of over 50 peer reviewed technical articles, which subjects include strategic planning, compliance, facility design, construction, operational excellence, and strategic long-range planning for the biotech Industry. Publication activities also include being the Lead Author of numerous industry reference guides for biomanufacturing and sterile product facility design, project management, and operations. This publication success has led to being an invited speaker at over 150 international industry forums, discussing various topics relating to strategic planning, program execution and GMP compliance issues. 

Global Industry influence and thought leadership is identified through activities such as completing the successful launch as Lead for the 3^rd Edition of the Biomanufacturing Facilities Baseline Guide, The Autologous Cell Therapies Good Practice Guide, and the Allogeneic Therapies Good Practice Guide for ISPE. Industry influence and thought leadership is also reflected in being a member of the ISPE and PDA Technical Training Faculties for both national and global training programs, an invited speaker to over 150 Industry conferences, a Teaching Fellow at NC State University’s Biomanufacturing Training and Education Cener (BTEC), and a sought-after reference in production of various Industry social media platforms.