Contract CDMO for viral vectors, cell therapies, and mRNA manufacturing
ProBio is a contract manufacturer focused on advanced therapies—viral vectors, cell and gene therapies, mRNA platforms, and antibody-drug conjugates. The tech stack is heavily industrial (SCADA, PLC, CMMS, UPS) rather than software-forward, reflecting their core competency in GMP-regulated manufacturing operations. Active projects cluster around viral vector scale-up, process technology transfer, and GMP lab buildout, while pain points center on yield optimization and translating research protocols into regulated production—typical friction points for a CDMO ramping manufacturing capacity.
ProBio is a contract development and manufacturing organization headquartered in Pennington, New Jersey, founded in 2020. They serve biotech and pharmaceutical companies seeking outsourced manufacturing for biologics, protein and mRNA vaccines, viral vectors, and cell and gene therapies. The organization spans 201–500 employees across engineering, manufacturing, operations, sales, and product functions, with active hiring in the United States, Japan, and China. Core capabilities include process development, GMP quality control, viral vector purification, engineered cell line generation, and lean manufacturing optimization.
ProBio manufactures viral vectors, mRNA vaccines, cell therapies, antibody-drug conjugates, and protein-based biologics for biotech partners. They provide full CDMO services including process development, technology transfer, and GMP-regulated production.
ProBio is based in Pennington, New Jersey and actively hiring across the United States, Japan, and China. Current open roles span engineering, manufacturing, sales, operations, and product functions.
Key focus areas include scaling viral vector production yield, process technology transfer from research to GMP, managing change control in regulated environments, and improving manufacturing capabilities across advanced therapy modalities.
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