Advisor/senior Advisor, Engineering, Biologics Drug Product Development

Eli Lilly

Base: $126,000 - $204,600; bonus: compyny bonus el...
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Parenteral drug product development
Cgmp and ich regulatory guidelines
Process control strategy definition
** Eli Lilly is seeking an Advisor/Senior Advisor for Engineering in Biologics Drug Product Development, responsible for defining clinical manufacturing processes for parenteral drug products and collaborating with cross-functional teams. The role requires significant industry experience in pharmaceutical development, particularly with biologics, and offers competitive compensation and benefits. **

Job Summary

  • This role is accountable for defining parenteral drug product clinical manufacturing processes along with associated control strategies for Eli Lilly's biologics portfolio.
  • The successful candidate will serve as a technical expert to drive technology transfer, manage risk assessments, and author regulatory documents for IND, BLA, and NDA submissions.
  • Eli Lilly offers a comprehensive benefit program including medical, dental, vision, 401(k) matching, and a company bonus based on performance.

Matching Summary

Match Score: 75

** Eli Lilly is seeking an Advisor/Senior Advisor for Engineering in Biologics Drug Product Development, responsible for defining clinical manufacturing processes for parenteral drug products and collaborating with cross-functional teams. The role requires significant industry experience in pharmaceutical development, particularly with biologics, and offers competitive compensation and benefits. **

Salary

Base: $126,000 - $204,600; Bonus: Company bonus eligible; Benefits: Medical, dental, vision, 401(k), vacation

Skills & Requirements

Must-have

  • Parenteral drug product development
  • cGMP and ICH regulatory guidelines
  • Process control strategy definition
  • Tech transfer and scale-up expertise
  • Biologics manufacturing experience

Nice-to-have

  • Experience with ADC and mRNA LNP technologies
  • Track record advancing products to BLA/NDA
  • Strong stakeholder influence skills
  • Statistical analysis and data management
  • Mentoring junior scientists

Key Requirements

  • PhD/MS/BS in Pharmaceutical Chemistry or Engineering
  • 2-12 years industry experience depending on degree level
  • Deep understanding of cGMP requirements and ICH guidelines

Work Rights

Not specified

Tailored Resume

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