Artosai
Solution Scientist
San Francisco
Sponsorship not specifiedDetected 56 days ago
LLMsFDA RegulatoryLeadershipCommunicationRegulatory Affairs
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odds of building a lasting career here
16Unrated
Cap-exempt (no lottery)0
Sponsors this role0
Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70
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About the role
- Evaluate AI-generated outputs for correctness, structure, and regulatory soundness
- Identify gaps, inconsistencies, and edge cases, and work with engineers to resolve them
- Communicate technical system behavior to non-technical users, and user needs back to engineers
Responsibilities
- Is excited by product design and system thinking, not just writing
- Help implement Artos in customer environments and support early adoption
Requirements
- Ability to analyze workflows and extract rules, patterns, and constraints
- Comfort reviewing structured or semi-structured system outputs (including AI-generated content)
- Ability to communicate clearly with engineers and product teams
- Ability to operate independently in a fast-moving startup environment
- Strong understanding of regulatory expectations across FDA, EMA, and ICH
- Experience working cross-functionally with regulatory, scientific, and technical stakeholders
- 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 written and verbal communication skills
Nice to have
- Familiarity with structured data formats (XML, JSON) is a plus
- Experience working with life sciences software tools is a plus
Skills
- It's a hybrid:
- part domain architect, part technical translator, part customer-facing problem solver.
Visa & Work Authorization
- You'll work across a wide range of content: CTD modules, internal summaries, briefing packages, templates, and sponsor-facing deliverables.
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This listing is sourced directly from Artosai's careers page and normalized into a canonical job model.