Pharma Domain Architect & Technical Translator

Artos AI

San Francisco (CA)

On-site

USD 140,000 - 210,000

Full time

3 days ago
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Job summary

Artos AI is seeking a domain-expert technical product lead with a strong pharma background to bridge engineering and end users. You will design and evolve systems that generate and manage regulatory and R&D documentation, especially in non-clinical and CMC domains, translating domain reality into actionable product requirements.

This hybrid role blends domain architecture with technical translation and customer-facing problem solving, requiring collaboration with medical writers, scientists, and

Qualifications

  • 3+ years in medical writing or regulatory affairs within pharma
  • Experience drafting CTD content (non-clinical or CMC)
  • Strong understanding of FDA, EMA, and ICH expectations
  • Cross-functional collaboration with regulatory, scientific, and technical stakeholders
  • Excellent written and verbal communication skills

Responsibilities

  • Deconstruct how regulatory 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 against real-world use cases
  • Communicate technical system behavior to non-technical users and relay user needs to engineers

Skills

Pharma domain knowledge
Technical translation
Cross-functional collaboration
Regulatory thinking
Communication skills

Tools

XML
JSON

Job description

Artos AI is seeking a domain-expert technical product lead with a strong pharma background to bridge engineering and end users. You will design and evolve systems that generate and manage regulatory and R&D documentation, especially in non-clinical and CMC domains, translating domain reality into actionable product requirements.

This hybrid role blends domain architecture with technical translation and customer-facing problem solving, requiring collaboration with medical writers, scientists, and

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