USFDA-audited CRO delivering in vitro and analytical testing for pharma
VitelyBio is a contract research organization (CRO) based in Ahmedabad, India, focused on in vitro bioequivalence, analytical characterization, and microbiological testing for pharmaceutical, nutraceutical, and cosmetic clients. The tech stack reveals dual operating modes: analytical chemistry instrumentation (HPLC, LC-MS/MS) paired with modern software engineering (Node.js, React, PostgreSQL, AWS) — indicating investment in lab data management and automation alongside wet-lab capabilities. Active hiring is skewed toward research roles, with process standardization and QMS strengthening as current pain points, suggesting the organization is scaling beyond founder-led operations.
VitelyBio operates as a USFDA-audited contract research organization providing in vitro bioequivalence studies, pharmaceutical characterization, dissolution development, and microbiological testing. The company serves pharmaceutical, nutraceutical, herbal, and cosmetic manufacturers across product development and lifecycle stages. Based in Ahmedabad with 51–200 employees, VitelyBio combines state-of-the-art analytical instrumentation (HPLC, LC-MS/MS, GCP) with custom protocol development and regulatory compliance expertise. The organization manages projects ranging from standard testing to complex studies, working to regulatory standards across R&D, quality, and compliance functions.
VitelyBio operates HPLC, LC-MS/MS, and related analytical instrumentation. The company is currently adopting advanced HPLC and LC-MS capabilities while running GCP infrastructure.
Backend and cloud: Node.js, PostgreSQL, AWS, GCP. Frontend: React, JavaScript. Analytics and lab data: SAS, R, JMP, Python. QA automation: Selenium, Playwright, Cypress. Mobile (iOS): Swift, Xcode, SwiftUI, RxSwift.
VitelyBio has 14 active open roles focused on research (5), engineering (4), and support functions. Current hiring is limited to India with minimal posting velocity.
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