Build the future of source-traced scientific reports.

PharmD, MSc, or PhD with hands-on formulation development experience. You will be the scientific authority of Pure Monograph — validating Build Monograph reports, refining formulation logic, and authoring the quality standards the pipeline generates against.

• 5+ years in pharmaceutical formulation development — solid oral, semi-solid, or parenteral
• Working knowledge of ICH Q1–Q12, USP / EP / JP, and 21 CFR Part 211
• Comfortable reading and critiquing formulation and stability reports in detail
• Strong scientific writing — you'll author the rules the platform follows

RAC-certified regulatory professional. You'll own the evidence-readiness of every report the platform produces — citations that resolve, measured versus predicted marked, gaps left as gaps. FDA, EMA, Health Canada, and ICH expectations inform the report design system. This seat owns evidence readiness, not document volume.

• RAC certification (US, EU, or global) and 5+ years in pharmaceutical regulatory affairs
• Direct experience reviewing scientific reports against FDA, EMA, Health Canada, and ICH expectations
• You know how regulators read evidence, and what must be refused when sources run out
• You translate those expectations into report behavior

Build the next modules of Pure Monograph. Extend the RAG pipeline, integrate new pharmacopeial and literature sources, and improve generation quality. You'll work directly with the founder and the formulation and regulatory leads.

• 4+ years building production systems with LLMs, RAG pipelines, or large-corpus retrieval
• Comfortable with FAISS or comparable vector stores, embedding models, and inference at scale
• Python fluency; FastAPI or similar backend experience
• Bonus: prior work on regulated or scientific document pipelines