Cheiron builds AI-native software for drug programs and is expanding into pharmaceutical CMC (Chemistry, Manufacturing, and Controls) teams. CMC governs how a drug is made, tested, and kept consistent throughout its commercial life, involving numerous regulatory commitments, post-approval changes, and cross-market submissions. Currently, this process relies on documents, spreadsheets, and institutional memory. Cheiron aims to augment these manual workflows with an intelligence and reasoning layer specific to CMC Regulatory. In this role, you will transform product concepts into engineering-ready specifications, collaborating across product, life sciences, and engineering teams. While the "what" and "why" of concepts will be provided, you will be responsible for defining the detailed "how." This includes determining how each component integrates with the existing architecture, what needs to be extended, what should remain unchanged, and outlining the build on paper before any coding begins. The CMC domain is specialized, with its own regulatory frameworks and workflows, but prior knowledge is not required. You will be supported by a life sciences team that manages the domain vocabulary and regulatory rules, and you will learn the domain through close collaboration. The key is your ability to immerse yourself in the subject matter until you can reason from first principles. This is a ground-floor opportunity at an early-stage company, offering direct work with founders, product/design, life sciences, and engineering teams. The role presents a steep learning curve, significant scope, and your specifications will directly impact pharmaceutical teams making critical regulatory decisions.
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Job Type
Full-time
Career Level
Entry Level