Description
Artos is hiring a domain-expert technical product lead to bridge engineering teams and pharma domain experts on systems that generate and manage regulatory and R&D documentation. The role translates document workflows and regulatory rules into product and engineering requirements, helps implement Artos in customer environments, evaluates AI-generated outputs, validates features, and communicates technical behavior to users and engineers. Candidates should have at least three years of experience in medical writing, regulatory affairs, or a closely related pharma role, direct CTD experience, and knowledge of FDA, EMA, and ICH expectations. The position requires in-person work in the Mission Bay office four to five days per week.
