GxP consulting for pharma manufacturing automation and compliance
i-Pharm GxP operates a consulting practice focused on GxP (Good Manufacturing Practice) compliance and operational technology in pharmaceutical manufacturing. The tech stack—SAP EWM, Ignition, PLC/SCADA systems (Allen-Bradley, Siemens, DeltaV), and AutoCAD Plant 3D—reveals a business centered on bridging IT/OT integration and warehouse automation in highly regulated environments. Current hiring is engineering-heavy (9 roles) with senior and lead-level emphasis, and active projects span greenfield pharma programs, automated material handling, and DeltaV control system implementations—all capital-intensive, GMP-critical work that demands deep domain expertise.
Notable leadership hires: Head of Validation
i-Pharm GxP is a New York-based consulting firm founded in 2014, serving pharma and biotech manufacturers across North America, Europe, and Asia-Pacific. The firm specializes in scoping, staffing, and delivering GxP compliance solutions, with particular focus on manufacturing automation, warehouse modernization, and process validation. Core capabilities include SAP EWM integration with operational technology systems, PLC/SCADA implementation, and control system design (DeltaV, Rockwell Automation, Siemens). The firm operates a lean internal team and builds project-specific delivery roadmaps rather than applying template solutions; all core work is performed in-house to maintain compliance rigor and avoid supply-chain complexity.
Primary tools: SAP EWM, Ignition SCADA platform, Rockwell Automation and Siemens PLC systems, DeltaV control systems, and AutoCAD Plant 3D for facility design. Stack reflects deep integration of IT systems with operational technology in GMP environments.
New York, New York. Founded in 2014, the firm operates across North America, Europe, and Asia-Pacific with U.S.-based hiring currently active.
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