Build the future of pharmaceutical regulatory intelligence.

PharmD, MSc, or PhD with hands-on formulation development experience. You will be the scientific authority of Pure Monograph — validating CTD outputs, refining formulation logic, and authoring the quality standards the platform 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 CTD Module 3 sections in detail
• Strong scientific writing — you'll author the rules the platform follows

RAC-certified regulatory professional. You'll own the regulator-readiness of every dossier the platform produces — ensuring alignment with FDA, EMA, Health Canada, and ICH expectations across the entire CTD Module 3.

• RAC certification (US, EU, or global) and 5+ years in pharmaceutical regulatory affairs
• Direct experience preparing or reviewing IND, NDA, ANDA, ANDS, or CTA submissions
• Deep familiarity with ICH M4Q(R2), Q9(R1), and Q12 in practice
• You translate regulator expectations into product 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