Advisor– Api/ds Network Contamination & Bioburden Control Strategy

Eli Lilly UK

Base: $129,000 - $189,200; bonus/equity: compyny b...
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7+ years pharmaceutical manufacturing experience
Deep understanding of contamination control requirements
Knowledge of cgmps and sterility assurance
** Eli Lilly UK is seeking an Advisor for their API/DS Network Contamination & Bioburden Control Strategy, focusing on contamination control across diverse manufacturing platforms. The ideal candidate will have over seven years of experience in pharmaceutical manufacturing, particularly in API processes, and will be responsible for ensuring compliance with regulatory standards while supporting new product introductions. **

Job Summary

  • This central position provides oversight and drives the harmonization of technical programs governing contamination control strategies across the Lilly API Network.
  • The role ensures control strategies align with regulatory guidance while supporting new product introductions, commercialization, and major process changes.
  • Lilly offers a comprehensive benefit program including medical, dental, vision, 401(k), pension, and well-being benefits alongside a competitive salary range.

Matching Summary

Match Score: 75

** Eli Lilly UK is seeking an Advisor for their API/DS Network Contamination & Bioburden Control Strategy, focusing on contamination control across diverse manufacturing platforms. The ideal candidate will have over seven years of experience in pharmaceutical manufacturing, particularly in API processes, and will be responsible for ensuring compliance with regulatory standards while supporting new product introductions. **

Salary

Base: $129,000 - $189,200; Bonus/Equity: Company bonus depending on performance; Benefits: Medical, dental, vision, 401(k), pension, vacation, wellness programs

Skills & Requirements

Must-have

  • 7+ years pharmaceutical manufacturing experience
  • Deep understanding of contamination control requirements
  • Knowledge of cGMPs and sterility assurance
  • Experience with viral safety strategies
  • Proficiency in environmental monitoring procedures

Nice-to-have

  • Strong influence and mentoring leadership skills
  • Experience with new site startup activities
  • Ability to drive continuous improvement initiatives
  • Engagement with external industry organizations
  • Cross-functional collaboration with PR&D teams

Key Requirements

  • BS/MS/PhD in biological science or engineering
  • Microbiology preferred background
  • 7+ years in pharmaceutical manufacturing
  • Experience with synthesis/fermentation/cell culture stages

Work Rights

Not specified

Tailored Resume

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