{"id":107132,"url":"https://alion.io/job/artos-solution-scientist","title":"Solution Scientist","company":{"id":7635,"name":"Artos","domain":"artosai.com","url":"https://alion.io/company/artos","size_band":null,"is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Ashby","truth_index":null},"role":"Science & Research","role_family":"Science & Research","seniority":"middle","employment_type":"full_time","work_mode":"hybrid","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["San Francisco, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":130500,"max":187000,"currency":"USD","period":"year","gross":null,"usd_annual":187000},"salary_estimate":null,"experience_years_min":3,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"LLM","optional":true}],"status":"live","first_seen_at":"2026-06-05T18:23:18Z","employer_posted_date":"2026-06-05","last_verified_at":"2026-11-02T21:27:36Z","board_verified":true,"closed_at":null,"days_open":150,"trust":{"level":"stale","repost_count":0,"flags":["stale"],"days_open":149},"description":"About Artos:\nAt 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.\nWe’re growing very fast, and we’re looking for adomain-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.\nThis 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.\nThe Role:\nAs a core member of Artos’s product team, you will act as the bridge between engineering and domain experts.\nYour 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\nduct.\nYou will work closely with:\nEnd users: (medical writers, regulatory professionals, scientists) to understand how documents are actually authored, reviewed, and quality-controlled in practice\n\nEngineering teams: to translate those workflows, constraints, and edge cases into system behavior\n\nProduct leadership: to shape feature scope, prioritization, and release readiness\n\nYou will help explain how the system works to users, collect feedback on where it breaks down, and communicate those insights back to engineering in a way that is precise, actionable, and technically useful.\nWhat You’ll Actually Do:\nThis role is about systems, not just documents.\nYou will:\nDeconstruct how regulatory and R&D documents are authored, reviewed, and QC’d in real organizations\n\nTranslate domain rules, conventions, and preferences into clear product and engineering requirements\n\nHelp implement Artos in customer environments and support early adoption\n\nEvaluate AI-generated outputs for correctness, structure, and regulatory soundness\n\nIdentify gaps, inconsistencies, and edge cases, and work with engineers to resolve them\n\nHelp validate features ahead of release by stress-testing them against real-world\n\nuse cases\n\nCommunicate technical system behavior to non-technical users, and user needs back to engineers\n\nYou’ll work across a wide range of content: CTD modules, internal summaries, briefing packages, templates, and sponsor-facing deliverables. You don’t need to be an expert in every document type on day one, but you do need to learn quickly and explain what you learn clearly.\nWho This Role Is For:\nThis role is ideal for someone who:\nComes from pharma or biotech and deeply understands regulatory documentation\n\nIs excited by product design and system thinking, not just writing\n\nEnjoys acting as a translator between technical and non-technical teams\n\nWants to shape how AI systems behave in regulated environments\n\nQualifications:\n3+ years of experience in medical writing, regulatory affairs, or a closely related pharma role\n\nDirect experience drafting, reviewing, or overseeing CTD content (especially non-clinical)and/or CMC)\n\nStrong understanding of regulatory expectations across FDA, EMA, and ICH\n\nExperience working cross-functionally with regulatory, scientific, and technical stakeholders\n\nStrong written and verbal communication skills\n\nRequirements:\nAbility to analyze workflows and extract rules, patterns, and constraints\n\nComfort reviewing structured or semi-structured system outputs (including AI-generated content)\n\nAbility to communicate clearly with engineers and product teams\n\nWillingness to be customer-facing and support implementation\n\nand feedback loops\n\nFamiliarity with structured data formats (XML, JSON) is a plus\n\nExperience working with life sciences software tools is a plus\n\nAbility to operate independently in a fast-moving startup environment\n\nOther Information:\nVery comfortable working in a fast-paced and intense startup environment\nWilling to work in-person in our office in Mission Bay 4-5 days/week\nLikes matcha KitKats, believes every LLM prompt is just Schrödinger’s cat waiting to be observed, and knows too many random facts about the Mongol postal 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