These design/build projects consisted of architectural/engineering, design, construction, and start-up of all systems for the upgrade and conversion of existing manufacturing suites for new therapeutic protein biosynthesis and purification processes at the Chiron Manufacturing Facility (CMF) in Emeryville, and the Vacaville Manufacturing Facility (VMF).
The Vacaville facility was one of the first local multi-host, multi-product fermentation facilities for the production of FDA licensed biological pharmaceutical products. Eichleay’s scope of work included the design of, and design modifications to, the processing and critical services utility systems for the cGMP pharmaceutical manufacturing processes at both facilities. A new HVAC system was also included for the CMF facility.
The scope of work included: methanol, ethanol, ammonium hydroxide, acetic acid, glycerol, oxygen, nitrogen storage and delivery systems; chromatography systems; depth filtration; solvent and purification waste systems. Deliverables included: preliminary design criteria; equipment layouts; P&IDs; data sheets; SOPs; automated functional requirements; procurement; construction support; system walkdowns and as-builts; and start-up assistance.
VMF and CMF Fermentation/New Purification Process Projects
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Transparency in Coverage (Federal ID: 26-1194667)