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
Business Strategy Development
Technology Assessment & Transfer
Project Management Consulting
Healthcare Facilities
Pharmaceutical, Biopharma
Conceptual project for bio-pharma plant
Strategies development
Budget, cost analysis, cost control
Chemical – pharma processes optimization
Engineering procedures
Due diligence
Feasibility studies bio, betalactam, non betalactam, anticancer plant
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