Paul Magreta has over 25 years of experience in bio-pharmaceutical operations in the United States and Europe, including leadership roles in business development, process engineering, process validation, and manufacturing science and technology (MSAT). He has led cross-functional global teams in facility design, start-up, and technology transfer for cGMP production of clinical and marketed biologics.

Paul has implemented lifecycle process validation for multiple commercial products, led the operational readiness for new facilities, and regularly presented and defended process validation strategies during audits and FDA inspections. He has worked in the UK, Italy, Germany, and Spain; managed tech transfers within the EU and has a working proficiency in Spanish.

Prior to consulting, Paul was responsible for developing a CDMO business within Grifols, was Head of Global Process Engineering at Novartis Vaccines and Diagnostics, and Head of Manufacturing Science and Technology at Genentech’s site in Porriño, Spain.

EDUCATION

University of Michigan
BSE, Chemical Engineering