Pharmaceutical engineering consulting for sterile process design and sustainability
Hyde E+C is a 30-year-old engineering consulting firm serving pharma and biopharma clients on process design, validation, and commissioning. The tech stack—Honeywell, Rockwell FactoryTalk, AutoCAD, Revit, Solidworks—reflects a capital-equipment and facility-design focus rather than software product development. Current project work centers on DCS/PLC/SCADA automation, clean-room commissioning, and cGMP equipment qualification, with hiring concentrated in engineering roles (senior and mid-level), suggesting active project delivery scaling rather than new-product expansion.
Hyde E+C provides end-to-end engineering consulting for pharmaceutical manufacturers and biopharma companies. The firm specializes in sterile process design, equipment validation, commissioning, and qualification of clean utilities and production facilities. With offices across the US, Europe, India, Singapore, Malaysia, and Canada, Hyde delivers global project capability across upstream and downstream processes, CIP systems, and regulatory compliance. Core service areas include 3D modeling, HVAC and BMS commissioning, computerized systems validation, and process automation—all oriented toward improving throughput while reducing water, energy, and chemical consumption.
Hyde uses Rockwell FactoryTalk (PLC/SCADA), Honeywell controls, AutoCAD, Revit, and Solidworks for equipment modeling and facility design. Documentum handles document management.
Yes. Hyde has 7 active roles, with 5 in engineering and 1 in research. Hiring spans senior and mid-level positions across the United States and India.
Current projects include automation of DCS/PLC/SCADA systems, clean-room and HVAC commissioning, cGMP equipment design for pharma, computerized systems validation, and 3D modeling for process piping and unit operations.
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