OVERVIEW
For more than three decades, PS&S has been a trusted design partner to the world's leading pharmaceutical and life science companies. We understand that manufacturing environments in this sector demand the highest levels of precision — where regulatory compliance, contamination control, and operational continuity are non-negotiable. Our integrated team of architects, engineers, and technical specialists brings deep industry knowledge to every engagement, delivering facilities that meet current Good Manufacturing Practice (cGMP) standards while remaining adaptable to evolving process and regulatory requirements.
TYPES OF FACILITIES
PS&S provides architecture and engineering design services across the full spectrum of pharmaceutical and life science manufacturing environments, including:
OUR APPROACH
PS&S designs biotech manufacturing environments with a focus on the technical disciplines that define bioprocessing excellence. Our approach encompasses clean manufacturing design, rigorous contamination control strategies, and comprehensive bioprocess integration. We bring specialized expertise in upstream bioprocessing, including fermentation and cell culture system design, and downstream bioprocessing, including chromatography, filtration, and purification train layout and utility support.
Our teams are experienced in the design and specification of both CIP/SIP and single-use technology systems for multiproduct manufacturing environments. We also have extensive experience in the containment of biohazards and the design of biowaste inactivation systems to ensure safe, compliant management of biological materials. Across all project types, we apply an integrated approach that aligns facility design, process systems, and regulatory strategy to deliver efficient, reliable, and compliant facilities.