Hubot is a CDMO focused on formulation, filling, and manufacturing of topicals, oral liquids, and skincare products across aerosol, tube, and jar formats. The operation runs on legacy industrial controls (Allen-Bradley PLC-5, HPLC) paired with modern compliance tools (Veeva Vault, LIMS), and is actively scaling microbiology and stability testing from the ground up while managing critical infrastructure upgrades—signaling both capability expansion and facility modernization pressure.
Hubot operates a turnkey CDMO in South Bend, Indiana, serving OTC, consumer healthcare, cosmetic, and medical-device brands. The company holds FDA registration for both pharmaceuticals and OTC products, plus ISO certifications across medical-device GMP, cosmetics GMP, quality, and environmental standards. Core capabilities span contract development, aerosol and liquid filling, formulation work, regulatory compliance, and supply-chain management. The 51–200 employee base is manufacturing-heavy, with active hiring in the United States and India focused on manufacturing, research, and quality roles.
Hubot is FDA-registered for pharmaceuticals and OTC products, EPA-registered, and holds ISO 13485 (medical-device GMP), ISO 22716 (cosmetic GMP), ISO 9001 (quality), ISO 14001 (environmental), plus Health Canada, TTB alcohol, ITAR, and organic certifications.
Current projects include building a microbiology lab in Winchester, scaling stability testing capability, formulation development, audit readiness, facility upgrades (electrical wiring to NEC standards), and preventive maintenance on compressors and boilers.
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