Sam Halaby

Sam has over 20 years of experience in master planning, programming, design, and qualification of biotechnology and pharmaceutical facilities ranging from clinical to full-scale production plants. Sam’s particular focus is on CGMP manufacturing design, including process technology evaluation, capacity analysis, potent compound handling, CGMP environmental classification, and operational analysis. Sam draws from his compliance and process experience to create and develop functionally compliant designs, integrating owner and regulatory requirements.

Sam has developed several unique design tools tailored to the early stages of project development. These design aids include production capacity modeling and assessment, manufacturing flow analysis, manufacturing flow diagrams, process logic diagrams, and environmental classification philosophy diagrams. Sam’s experience is international and he has filled the role of project manager and process lead on major capital projects through construction.