You will own a content domain end to end, move multiple data-validated concepts into production, maintain accurate and current source documentation, contribute to at least one AI-assisted improvement in how content is built, set up a repeatable process for tracking new approvals, label changes, and HCPCS updates, and show measurable results in edit accuracy, speed, or client value. You will learn Machinify's content portfolio, source library, technology, and development process; build working relationships with Product and Data Science; assess current drug editing coverage against high-cost therapeutic areas; and deliver a prioritized list of specialty drug content gaps and opportunities.