With over 30 years of experience in big pharma, including roles at Bristol Myers Squibb and Catalent, Mario Baccaro has worked in key positions across Europe, Africa, Asia, and Australia. His expertise includes implementing best practices and guidelines, developing and designing concepts, managing capital projects, strategizing technology and engineering plans, analyzing future plant technologies, and estimating costs and scope. Throughout his career, Mario has focused on engineering conceptual innovations while ensuring compliance with GMP, FDA, and EMA regulations.

• Engineering assessment analysis comparison investment impact, capital budget, cost control

• Development and optimization of chemical / pharmaceutical processes for biopharma products

• Analysis value and consistency of project for future industrial use

• Faesability concept development and design for chemical/pharmaceutical plants

• Planning, development, approval and implementation on projects, network, strategy tecnology

• Best practices and guidelines GMP, FDA, EMA procedure