Ce & Ic
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We've assisted our clients in the successful completion of hundreds of critical projects, and we'd welcome the opportunity to work with you. We are proactive in finding brilliant solutions for our clients that best achieve their goals and plans. We recognize the importance of innovation and fostering a culture of continuous improvement.

The process of building a workforce for the future requires tremendous adaptability and vision. In many cases, we begin working with our clients in the early stages of their projects to develop the process and facility requirements, site requirements, equipment lists, sizing and availability of supporting infrastructure, space planning, layouts and equipment arrangements, process flow diagrams, automation philosophy, alternate approaches, etc.
Services
CE&IC is a full-service engineering and architectural design firm established in 1984 and focused specifically on serving the pharmaceutical, biotechnology and specialty chemical industries. We provide our services on projects located across the United States and some internationally. CE&IC is recognized as a leader in the planning and design of cGMP development and manufacturing facilities.
CE&IC employs a full-time staff of engineers, architects, and designers. We can provide a full range of design support for our clients' projects utilizing our resources in process, mechanical, instrumentation and controls, electrical, structural and civil engineering as well as architecture and CAD/3D design.
CE&IC employs a full-time staff of engineers, architects and designers to deliver our client's projects from our office in Burlington, New Jersey. CE&IC is always looking for qualified engineers, architects, and CAD/3D designers to join our team.

Please respond to the positions identified below if your career goals include continued professional development, working in a fast paced environment, and assisting professional clients in the development of technical solutions.CE&IC is a highly regarded engineering and design consulting firm established in 1984 and focused on serving the pharmaceutical and biotechnology industries.
CE&IC has successfully completed hundreds of GMP development and manufacturing projects for our bio/pharmaceutical clients. Our primary practice areas include Biologics, API's, Sterile Fill/Finish, Oral Solid Dosage forms, Liquid Dosage forms, and Highly Potent Compounds.

Within these practice areas, we can assist our clients in delivering their projects from planning and concept development through preliminary and detailed design, procurement, construction assistance, commissioning and validation.Please find following an overview of CE&IC's capabilities within each of these practice areas.
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