Advisor, Analytical Development-cmc (cell and Molecular Biology)

Eli Lilly Eli Lilly · Pharma · Indianapolis, IN

Develops and optimizes analytical methods for RNA drug substances and LNP products in a healthcare setting, partnering with cross-functional teams and ensuring compliance with regulations.

What you'd actually do

  1. Lead the development, optimization and qualification of analytical methods intended for a variety of purposes, including release and stability testing, product characterization, high-throughput analysis, and characterization of complex raw materials.
  2. Partner across the Analytical Development team and cross-functionally with BR&D and SMDD to lead, plan, and execute complex studies; serve as the analytical lead in cross-functional interactions.
  3. Develop and implement methods intended for product characterization to support late stage and commercialization of gene editing programs.
  4. Work in partnership with internal and/or external QC to coordinate analytical method transfer within the organization or at Contract Manufacturing Organizations (CMOs)/Contract Testing Laboratories (CTLs).
  5. Provide technical oversight for troubleshooting and phase-appropriate qualification and validation of analytical assays for the analysis of gRNA, mRNA, and LNP.

Skills

Required

  • PhD in Molecular Biology, Cell Biology, Biochemistry, Microbiology or a related field, with 5+ years of experience in biotech/pharmaceutical industry, specifically in cell-based assay development.
  • MS in Molecular Biology, Cell Biology, Biochemistry, Microbiology or a related field, with 10+ years of experience in biotech/pharmaceutical industry, specifically in cell-based assay development.
  • Hands-on experience developing and troubleshooting molecular and cell-based analytical methods applied to complex and heterogeneous systems.
  • Excellent scientific knowledge in biochemistry, cell biology and molecular biology with a conceptual understanding of strategies for method development and troubleshooting.
  • Experience in assay development, qualification, validation, and implementation to support target candidate validation from non-GxP to GMP environments.
  • Familiarity with applicable ICH regulations and multi-compendial guidelines related to method validation.
  • Proactive, creative, ability to work effectively on cross-functional teams and positive attitude.
  • Effective oral and written communication skills.
  • Proven people leadership skills.

Nice to have

  • Experience in developing cell-based potency assays is highly preferred.
  • Advanced understanding of lipid nanoparticle delivery, production, and purification is a plus.
  • Knowledge/hands-on experience in automation and liquid handlers are desirable but not required.

What the JD emphasized

  • cell-based assay development
  • method development and troubleshooting
  • cell-based potency assays
  • lipid nanoparticle delivery
  • assay development, qualification, validation, and implementation
  • ICH regulations
  • multi-compendial guidelines