← All roles

Solution Scientist

Artos· Operations
Apply on company site
Mission Bay, San Francisco$131k - $187kFull-timePosted 1mo ago

About the role

Domain-expert technical product lead to bridge engineering and life-sciences domain experts, designing and implementing systems for regulatory and R&D documentation in pharma/biotech environments.

Responsibilities

  • Deconstruct how regulatory and R&D documents are authored, reviewed, and QC’d in real organizations
  • Translate domain rules, conventions, and preferences into clear product and engineering requirements
  • Help implement Artos in customer environments and support early adoption
  • Evaluate AI-generated outputs for correctness, structure, and regulatory soundness
  • Identify gaps, inconsistencies, and edge cases, and work with engineers to resolve them
  • Help validate features ahead of release by stress-testing them against real-world use cases
  • Communicate technical system behavior to non-technical users, and user needs back to engineers
  • Work across content types: CTD modules, internal summaries, briefing packages, templates, sponsor-facing deliverables

Qualifications

  • 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-functional with regulatory, scientific, and technical stakeholders
  • Strong written and verbal communication skills

Skills

Required:Medical writingCTD content drafting/reviewingRegulatory knowledge (FDA/EMA/ICH)Cross-functional collaborationCommunicationTechnical translationCustomer-facing/implementation support
Nice to have:Structured data familiarity
Last updated Oct 21, 2026. Interested? Apply on the company site.
Artos logo

About Artos

Authoring documents for life sciences in minutes, not months.

Artos is an AI-based document-drafting platform that helps life sciences companies turn their data into critical documents in minutes. These submissions currently take months and are the final hurdle before life sciences companies are allowed to sell their product.

Company profileWebsite

More open roles at Artos