I pursue the advancement of innovative technology platforms that deliver value to the Biotechnology Industries. I partner with individuals and companies who seek to grow the impact they deliver. Inquiries are welcome.

Responsible for bioprocess development from early clinical development through commercial life-cycle management spanning cell line, cell culture, purification, analytical, scale-up, technology transfer, process validation, registration and life cycle management for commercial products, R&D pipeline development programs and contract manufacturing client programs at facilities located in Worcester MA, Puerto Rico and Singapore. Leading a team of 150+ world-class BS, MS and PhD level scientist.

Responsible for the process development and manufacture of biologics drug substance in support of commercial, clinical and contract manufacturing product portfolios. Management responsibilities included oversight of Biologics Production and Engineering at the Worcester, MA facility and Global Process and Manufacturing Sciences with a total of 530 employees across 4 sites located in Worcester, MA, Barceloneta, Puerto Rico, Redwood City, CA and Singapore. Manufacturing portfolio included 3 commerc

Responsible for the manufacture of biologics drug substance in support of commercial, clinical and contract manufacturing product portfolios. Management responsibilities included oversight of Biologics Production and Engineering Departments with a total of 230 employees including four integrated manufacturing suites equipped with 3,000L and 6,000L bioreactors for mammalian cell culture and downstream operations to bulk fill of drug substance, core support, media/buffer prep, planning, logistics,

Responsibilities included strategic management of the biologics drug substance manufacturing portfolio including commercial, clinical and contract manufacturing. Management responsibilities included 5 direct reports including 2 PhD level Chemistry, Manufacturing and Controls (CMC) Directors and 3 Project Managers with significant matrix leadership responsibility for successful execution of multiple internal clinical development drug substance CMC/manufacturing programs and multiple third parties

Held multiple roles of increasing responsibility culminating in Director, Protein Biology.

Laboratory supervisor with 3 direct reports focused on the design, development and implementation of protein purification processes for the large-scale cGMP manufacture of therapeutic proteins. Project leader for cGMP manufacture of Phase I clinical supply of therapeutic protein for contract manufacturing customer. Member of the D2E7 clinical supply manufacturing team, a fully human anti-TNFα monoclonal antibody now marketed by AbbVie as HUMIRA.