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CMC Workflow Specialist; Analytical​/Tech Transfer

Job in New York, New York County, New York, 10261, USA
Listing for: Raycaster
Full Time position
Listed on 2026-03-01
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
  • IT/Tech
    Data Analyst, Data Scientist
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Position: CMC Workflow Specialist (Analytical/Tech Transfer)
Location: New York

About Raycaster

We build AI agents for life sciences. Backed by leading life sciences investors and YC, we’re already working with Agilent, Yokogawa Life Sciences and many leading companies to automate their regulated, complex processes to accelerate drug development.

The role (what you’ll do)
  • Partner with CMC teams to map current workflows end-to-end (inputs, systems, approvals, artifacts).
  • Decompose tech-transfer packages (method revs, redlines/rationales, representative chromatograms, acceptance tests) into steps an AI can execute with citations.
  • Capture validation/stability/release processes (accuracy/precision/linearity/LOQ, OOT rules, spec checks, CoAs) and translate them into checklists, schemas, and templates.
  • Define data and document requirements (e.g., LIMS/CDS exports, S3/SharePoint/Vault locations), edge cases, and “fail-closed” rules (no source → no claim).
  • Review AI-generated drafts for scientific correctness and compliance expectations (21 CFR Part 11).
  • Create clear SOPs/playbooks for each automated workflow; iterate with engineers to reach “ready for pilot” quality.
You might be a fit if you have
  • 3 years in CMC/Analytical Development or QC
    , ideally touching Phase 2/3 or tech transfer to CRO/CMO/CDMO.
  • Hands‑on with HPLC/LC-MS (Ion‑Pair, HILIC, AEX), method/SOP authoring, and interpreting system‑suitability & chromatograms.
  • Built or reviewed validation packets (ICH Q2(R1/R2)),
    stability trending/OOT,
    release specs/Co As , and change control narratives.
  • Operated in non‑GMP → GMP handoffs; practical understanding of 21 CFR Part 11 expectations (audit trail, e‑sig routing, data integrity).
  • Familiarity with at least some of:
    Veeva Vault (or Master Control),
    ELN/LIMS (Benchling, Lab Ware, Sample Manager),
    CDS (Empower/Chromeleon),
    Jira/Service Now
    .
  • Comfort collaborating with engineers; you enjoy turning tacit know‑how into templates, schemas, and acceptance criteria
    .
Nice to have
  • ASO, mRNA/LNP, peptides, or oligo experience;
    Phase 3/registration exposure.
  • Awareness of CSV (computerized system validation), ALCOA+, and doc control practices.
  • Light data skills (reading CSVs, understanding units/columns) and curiosity about AWS/S3/Athena‑style data lakes.
Why this is interesting

You’ll help design the cutting edge of audited AI workflows that save teams hours per artifact while keeping reviewers in control. Your fingerprints will be on how modern CMC gets done.

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