Pharmaceutical & Life Sciences
Validated control systems for cGMP manufacturing, clean rooms, and the environments where product quality is non-negotiable.
Validated control systems for cGMP manufacturing, clean rooms, and the environments where product quality is non-negotiable.
Pharmaceutical and life sciences facilities operate under regulatory regimes that leave little room for interpretation. Environmental conditions, batch records, and system performance must all be documented, validated, and audit-ready. EES has been delivering control systems into this environment for clients including Eli Lilly for decades — work characterized by validation-grade rigor and the kind of detail that withstands FDA scrutiny.
From clean room HVAC and pressure cascade control to process automation for manufacturing suites and Validation IQ/OQ/PQ documentation, we bring the regulatory discipline that life sciences clients require.
Pressure cascade control, temperature and humidity management, particulate monitoring integration, and the documented performance characteristics regulators expect. Designed for ISO classifications and grade requirements from controlled non-classified space through Grade A.
PLC and DCS-based automation for pharmaceutical manufacturing suites — batch sequencing, recipe management, electronic batch records integration, and operator interfaces designed for production realities.
Full IQ, OQ, PQ documentation packages. Change control support, requalification programs, and the evidence packages that survive audit. Our validation work has supported regulatory submissions for some of the largest names in pharmaceutical manufacturing.
Custom process skids with integrated controls, instrumentation, and validation documentation. Factory acceptance testing at our Warren, NJ facility with full FAT documentation.
BMS systems engineered for the environmental tolerances life sciences facilities require — with the alarm management, trending, and reporting needed for both operations and compliance.
“Reviews and behind-the-scenes work seemed to always be complete and we did not have to work with you on improving performance at all. That has been a great relief, as I generally have to hold hands with the contractor.”
— Dan Grill, Eli Lilly Sr. Process Automation Engineer
Pharmaceutical projects benefit from early engineering conversations. Whether you are scoping a new facility, evaluating a retrofit, or reviewing service coverage on an existing validated system, we are happy to start the conversation.