Generative AI Medical Writing Solution for Biotech, Life Sciences, Pharma & Medical Devices | Artos AI. Book a demo online. Backed by Y Combinator.
About the role
As a core member of Artos’s product team, you will act as the bridge between engineering and domain experts. Your primary responsibility will be to help design, implement, and evolve systems that generate and manage regulatory and R&D documentation—particularly in the non-clinical and/or CMC domains—by ensuring that domain reality is faithfully represented in the pro
What they're looking for
- 3+ years of experience in medical writing, regulatory affairs, or a closely related pharma role
- Direct experience drafting, reviewing, or overseeing CTD content (especially non-clinical)and/or CMC)
- Strong understanding of regulatory expectations across FDA, EMA, and ICH
- Experience working cross-functionally with regulatory, scientific, and technical stakeholders
- Strong written and verbal communication skills
- Ability to analyze workflows and extract rules, patterns, and constraints
More about this role
At Artos, we build tools that help biopharma companies create and manage their R&D documentation in a fraction of the time. If you’re looking to join a team whose mission is to fundamentally change the way that drug development gets done, we’d love to talk to you.
We’re growing very fast, and we’re looking for a domain-expert technical product lead —someone with a strong pharma background who can sit between engineering teams and end users, help implement our system in real customer environments, and translate deeply technical capabilities into workflows that actually make sense to scientists, medical writers, and regulatory teams.
This is not a traditional product manager role, nor a traditional medical writing role. It’s a hybrid: part domain architect, part technical translator, part customer-facing problem solver.
As a core member of Artos’s product team, you will act as the bridge between engineering and domain experts.
Your primary responsibility will be to help design, implement, and evolve systems that generate and manage regulatory and R&D documentation—particularly in the non-clinical and/or CMC domains—by ensuring that domain reality is faithfully represented in the...
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