OUR LEADERSHIP

Experienced people. A new standard for softgel manufacturing.

Ryte brings together experienced leadership in manufacturing, operations, and quality to build a dedicated softgel manufacturing operation where quality and accountability guide every decision.
THE PEOPLE BEHIND RYTE

Experience that sets the foundation.

Ryte's leadership brings together experience in manufacturing operations, facility development, and quality oversight. Together, they're building a dedicated softgel manufacturing operation centered on consistency, accountability, and long-term partnerships.
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Scott Pecora

Founder & CEO
Scott brings extensive experience in manufacturing operations, facility development, and large-scale production environments. His expertise in building and optimizing manufacturing facilities, investing in advanced equipment, and developing efficient operations helps establish the foundation for Ryte's long-term success. His focus on operational excellence, infrastructure, and quality-driven manufacturing ensures Ryte is built to support both current production needs and future growth.
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Brad McCurley

President & Co-Founder
Brad brings 13 years of manufacturing experience, including seven years specializing in softgel manufacturing. His focus is on building transparent partnerships and dependable manufacturing processes that brands can trust.  
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Barry Brown

VP of Quality & Regulatory

Barry is a biochemist with more than 30 years in pharmaceutical, nutraceutical, and specialty chemical manufacturing, and he has worked on both sides of the audit table. As a GMP certification auditor for NSF International, he audited supplement manufacturers against 21 CFR 111 and NSF/ANSI 173. At a nutraceutical contract manufacturer, he built the quality system from the ground up and led the facility through its first NSF cGMP certification.

His experience covers every step from the lab to finished product release: analytical chemistry and method validation, multi-site quality control, supplement formulation, and manufacturing for Phase I and II NIH-sponsored clinical trials.

At Ryte, Barry leads the quality program. It is built to 21 CFR 111 from day one, so it’s in place before the first batch rather than after the first audit.

B.S. Biochemistry, Virginia Tech

LET'S WORK TOGETHER

Experienced people. Ready to hear your ideas.

Whether you're developing a new softgel product or planning future manufacturing needs, our team is ready to learn about your project and discuss the next steps.