You solve product problems end to end. You go deep into how CMC and regulatory teams actually work and how they use our product: how a manufacturing change moves from the plant through QA and regulatory affairs to a filing in each market, who decides what, and where today’s tools fail them. You keep going until you understand the problem better than the brief that named it, then turn it into real user workflows, engineering-ready specs, and data models, settled on paper before a line of code is written.
CMC is a specialized world with its own regulatory frameworks and its own workflows. You do not need to know it coming in. You’ll learn it first-hand, from the regulations and guidance themselves, from customers’ own trackers and filings, and from the people who do the work, with a life sciences team alongside you who own the regulatory rules and check your reasoning. What matters is that you’re the kind of person who immerses until you can reason from first principles.
This is a ground-floor role at an early-stage company. You’ll work directly with the founders and the product/design, life sciences, and engineering teams. The learning curve is steep, the scope is real, and your specs go directly to pharma teams making real regulatory decisions.