Re:Build Manufacturing at INTERPHEX 2026

Re:Build Manufacturing will be attending INTERPHEX, taking place April 21-23 at the Javits Center in New York, NY. As one of the premier trade shows for pharmaceutical and biotech manufacturing innovation, INTERPHEX brings together industry leaders, plant managers, engineers, and operations professionals to explore advances in production capabilities, regulatory compliance, and the path from clinical trials to commercial manufacturing.

Visit Re:Build at Booth #3854 to connect with our team of process engineers and fabrication specialists. 

We work with pharmaceutical and biotech manufacturers, applying our deep process engineering expertise to design, fabricate, and deliver custom-engineered systems that support safe, compliant scale-up in demanding regulated environments.

What sets Re:Build apart is our fully integrated approach to pharmaceutical scale-up across the full production lifecycle. We combine process engineering, custom fabrication, automation, installation, and validation under one roof, reducing vendor complexity and accelerating time to market in highly regulated environments. 

From modular skid-based systems and custom process equipment to equipment upgrades and site installation with SAT validation, Re:Build helps organizations reduce risk, accelerate time to market, and bring pharmaceutical and biotech products to market with confidence.

Featured Capabilities

Re:Build delivers advanced solutions tailored specifically to pharmaceutical and biotech manufacturers, including:

• Process skid fabrication: Modular, skid-based systems including custom process skids, CIP/SIP skids, and mixing & dosing systems designed for fast deployment and seamless validation
• Custom process equipment, including pressure vessels, reactors, filtration systems, and drying systems engineered for product integrity
• Equipment upgrades and system modifications to extend asset life, improve efficiency, and maintain compliance without costly revalidation
• System integration and controls engineering that seamlessly connects new equipment with legacy systems using advanced automation
• Site installation, commissioning, and Site Acceptance Testing (SAT) validation to ensure compliance and minimize disruption
• Onsite skilled trades and maintenance support from certified technicians who understand pharma compliance requirements

Our team combines deep process engineering knowledge with proven execution to help pharmaceutical and biotech producers reduce downtime, strengthen operational reliability, and scale production confidently in highly regulated environments. 

We support critical applications including API manufacturing, biotech process development, pharmaceutical packaging, powder processing & granulation, and solvent processing.

Why Re:Build

Re:Build Manufacturing brings U.S.-based engineering and implementation expertise, including ISO 9001:2015 certification, ASME U&R Stamp registration, and UL508A listed panel shop capabilities. These credentials matter in regulated pharmaceutical environments where documentation, traceability, and compliance are non-negotiable at every stage of a project., 

Whether you are scaling a new therapeutic, upgrading aging equipment, or redesigning a production facility, Re:Build partners closely with clients to transform operations into safer, more efficient, and more compliant environments.

Connect at INTERPHEX 2026

Stop by Booth #3854 to discuss your upcoming projects with the Re:Build team.

Business Development Contact

Cait Boyd
Cait.Boyd@optimation.us