Lead radiopharmaceutical analytical chemistry at Lilly, advancing method development and validation for phase 1b through phase 3 programs. This technical role supports GMP readiness.

The Advisor, Analytical Chemist serves as the primary analytical chemistry subject matter expert within RLT Chemistry, Manufacturing & Controls Technical Operations. You will guide chromatographic and spectroscopic methods, regulatory documentation, and analytical readiness. Collaboration spans QC, CMC Regulatory, manufacturing, and external CDMO partners.

Key Responsibilities:
Lead analytical method development for APIs and drug products
Optimize HPLC, UPLC, TLC, GC, and spectroscopic methods
Author validation protocols, reports, and regulatory submission sections
Transfer validated methods to QC laboratories and CDMOs




Support investigations, audits, and analytical technology improvements

Requirements:
Bachelor's degree in chemistry, analytical chemistry, or organic chemistry
10+ years in GMP analytical development, validation, or testing
Expertise validating chromatographic and spectroscopic analytical methods
Knowledge of GMP, FDA, EMA, ICH, USP, and PDA guidelines
Canadian citizenship and solid technical communication skills

Apply analytical chemistry expertise, method validation leadership, and GMP knowledge to Lilly radiopharmaceutical programs and regulatory readiness.
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📌 Advisor Analytical Chemistry Radiopharmaceuticals Toronto
🏢 590 Point Canada
📍 Toronto