Participation in one of Switzerland’s largest pharmaceutical Fill & Finish projects, supporting the creation of advanced sterile manufacturing capacity for the biopharmaceutical industry.
The scope included HVAC and cleanroom systems for GMP-controlled areas, with a strong focus on contamination control, environmental conditions, pressure cascade philosophy, commissioning readiness and qualification support.
This project represents a key milestone in my professional experience, combining large-scale pharmaceutical engineering, cleanroom technology and CQV execution in a highly regulated environment.
Over 20 years of experience in Sterile, Biological Pharmaceutical and Hospital Facilities Engineering Design, Construction and Validation.





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