Principal Scientist, Analytical Development - Gene Therapy

Eli Lilly UK

Indianapolis, Indiana, US
Base: $71,250 - $187,000; bonus/equity: compyny bo...
Analytical method development in regulated environment
Characterizing aav viral vectors
Performing bioassays and elisa
The Development Analytical Development group at Lilly Harborside Laboratories is seeking a Scientist to provide analytical assay development, optimization and routine testing of AAV viral vectors

Job Summary

  • The Development Analytical Development group at Lilly Harborside Laboratories is seeking a Scientist to provide analytical assay development, optimization and routine testing of AAV viral vectors.
  • Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits; life insurance and death benefits; and well-being benefits.
  • Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.

Matching Summary

The Development Analytical Development group at Lilly Harborside Laboratories is seeking a Scientist to provide analytical assay development, optimization and routine testing of AAV viral vectors.

Salary

Base: $71,250 - $187,000; Bonus/Equity: Company bonus depending on performance; Benefits: Comprehensive benefits including 401(k), pension, medical, dental, vision, life insurance, and wellness programs

Skills & Requirements

Must-have

  • Analytical method development in regulated environment
  • Characterizing AAV viral vectors
  • Performing bioassays and ELISA
  • Technical documentation and data integrity
  • Project leadership in analytical development

Nice-to-have

  • Mentoring junior scientists
  • Managing external CRO and CDMO collaborations
  • Experience with mammalian cell culture
  • Strong written and verbal communication
  • Cross-functional team collaboration

Key Requirements

  • Bachelor’s degree with 10+ years or Master’s degree with 8+ years experience
  • Experience supporting gene therapy or advanced modalities
  • Authorized to work in the United States full-time
  • Experience in GMP regulated environment
  • Proven leadership in technical strategy and risk assessment

Work Rights

Authorized to work in the United States full-time

Tailored Resume

Cover Letter