- Learn how a CDMO can be a Customer-Driven Manufacturing Organization
- How CDMOs can use digital infrastructure to make the experience from technology transfer all the way through lifecycle management more customer-focused
- How CDMOs can partner to integrate the supply chain to simplify processes and increase reliability
- How strategic investments by customers with CDMOs can create value for both customer and CDMO
JR Humbert
VP, Quality
INCOG BioPharma Services
JR Humbert is currently the VP, Quality at INCOG BioPharma Services, and created and implemented the quality system at INCOG, which in three years went from company creation through successful FDA inspection in 3 years.
JR has over 20 years of pharmaceutical and biotechnology industry experience in validation, quality, technology transfer, process engineering, and program management. Some of JR’s previous companies include Piramal Pharma Solutions, Roche/Genentech, Hospira, and Cook Pharmica.
JR has participated in multiple global health authority inspections and developed inspection responses. JR has an MBA from Indiana University, and a BA in Chemistry and Biochemistry from the University of Colorado-Boulder.
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INCOG has been designed and built from decades of experience with a clear purpose: to deliver better CDMO services in the injectable drug product space.
With our dedicated team, best-in-class processes, and state-of-the-art equipment, we deliver meaningful results and stand-out customer experiences. We are here to strive for the best—for our team and for our customers. We are in it with you from the moment we start work on your project. We go above and beyond to understand your requirements, meet your needs, and foster a truly collaborative partnership.
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Founded in June 2020, INCOG BioPharma Services offers development and manufacturing services to both early phase and late phase biopharmaceutical companies. We are located on the northeast corner of Indianapolis in Fishers, IN.
