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IPS is a recognized leader in delivering technical services to help our clients succeed with their capital programs.
Our core services are centered on the design, construction, validation and commissioning of regulated facilities.
Working for Over
700 Pharma and Bio Clients throughout the
world, the IPS perspective is unique. Our single-source capability encapsulates pharmaceutical facility and process equipment engineering, construction management, environmental and complete compliance and commissioning services. We focus our resources on formulating solutions that meet your criteria and your bottom line. It takes a unique blend of experience and skills to effectively program new facilities and reprogram existing facilities. IPS and many of our staff are ex-pharmaceutical operators; industry trained professionals.
Founded in 1989 by engineers having worked from an Owner's perspective, our firm has grown to more than 300 professionals
serving multiple regions of the United States,Puerto Rico
and India. IPS' unique approach has enabled us to develop the full range of services in-house. Through the integration of design, construction and validation, projects can be locked into a target cost, often times with a single-source of accountability and always a unified goal. This full range of services can be bundled and unbundled, to best fit the project condition and parameters. IPS views a project in the full range, whether or not we are involved with all aspects of the project. Accordingly, we have designed and developed projects more successfully and with less rework than is seen elsewhere. We have created
a set of engineering and management
principles that all IPS personnel know and live by.
Our unique blend of professionals apply expertise across a variety of projects including all types of pharmaceutical manufacturing and related clean-industry programs conducted by biotechnology, healthcare, semiconductor and food industries.
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Member USGBC
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