Associate Director - Quality - (qc – Endo Micro)

Eli Lilly UK

Houston, TX, US
Base: $123,000 - $198,000; bonus/equity: compyny b...
Cgmp compliance and manufacturing guidance
Analytical methods for small molecules
Technical leadership in quality control
The Associate Director QC – Endo Micro will be part of the startup team for a greenfield manufacturing site in Houston, TX, helping to build processes and enable successful GMP manufacturing operations

Job Summary

  • The Associate Director QC – Endo Micro will be part of the startup team for a greenfield manufacturing site in Houston, TX, helping to build processes and enable successful GMP manufacturing operations.
  • This role involves providing technical leadership, coaching staff, ensuring GMP compliance, and collaborating across functions to meet quality and business objectives.
  • Lilly offers a comprehensive benefits program including 401(k), pension, medical, dental, vision, life insurance, and well-being benefits, with an anticipated salary range of $123,000 - $198,000 plus potential bonuses.

Matching Summary

The Associate Director QC – Endo Micro will be part of the startup team for a greenfield manufacturing site in Houston, TX, helping to build processes and enable successful GMP manufacturing operations.

Salary

Base: $123,000 - $198,000; Bonus/Equity: Company bonus eligible; Benefits: Comprehensive benefits including 401(k), pension, medical, dental, vision

Skills & Requirements

Must-have

  • cGMP compliance and manufacturing guidance
  • Analytical methods for small molecules
  • Technical leadership in quality control
  • GMP manufacturing operations startup
  • Cross-functional collaboration
  • Process optimization and technical projects

Nice-to-have

  • Project management skills
  • Experience with Empower software
  • Experience with Process Analytical Technologies
  • Experience with LIMS implementation
  • Strong analytical and quantitative problem-solving
  • Ability to influence diverse groups
  • Strategic thinking and relationship building

Key Requirements

  • Bachelor’s Degree in scientific discipline
  • 5+ years Quality Control and leadership experience
  • Authorization to work in the United States
  • Extensive knowledge of pharmaceutical analytical methods

Work Rights

Must be authorized to work in the United States without sponsorship

Tailored Resume

Cover Letter