Director, Engineering, Parenteral (m2-m3)

Eli Lilly UK

Concord, NC, US
Base: $186,767.00 py; bonus/equity: compyny bonus ...
Automation system expertise
Cgmp environment experience
Biopharmaceutical equipment knowledge
Eli Lilly and Company seeks a Director, Engineering, Parenteral (M2-M3) to lead a team of professionals in delivering the full scope of parenteral/DAP systems—from user requirements through design, build, commissioning, qualification, validation, and operation—while supporting site leadership in building a diverse, engineering-driven organization

Job Summary

  • Eli Lilly and Company seeks a Director, Engineering, Parenteral (M2-M3) to lead a team of professionals in delivering the full scope of parenteral/DAP systems—from user requirements through design, build, commissioning, qualification, validation, and operation—while supporting site leadership in building a diverse, engineering-driven organization.
  • Achieve business goals related to safety, quality, and process efficiency by maintaining performance metrics and driving improvements.
  • Lilly offers a comprehensive benefit program including 401(k), pension, medical, dental, vision, life insurance, and well-being benefits, along with eligibility for company bonuses based on performance.

Matching Summary

Eli Lilly and Company seeks a Director, Engineering, Parenteral (M2-M3) to lead a team of professionals in delivering the full scope of parenteral/DAP systems—from user requirements through design, build, commissioning, qualification, validation, and operation—while supporting site leadership in building a diverse, engineering-driven organization.

Salary

Base: $186,767.00 per year; Bonus/Equity: Company bonus eligibility; Benefits: Comprehensive benefits program including 401(k), pension, medical, dental, vision, life insurance, and well-being benefits

Skills & Requirements

Must-have

  • Automation System expertise
  • cGMP environment experience
  • Biopharmaceutical equipment knowledge
  • Parenteral/DAP systems lifecycle
  • On-call availability
  • Domestic and international travel

Nice-to-have

  • Continuous Improvement initiatives
  • Regulatory agency engagement
  • Diversity and inclusion support
  • Change management tools experience
  • Employee resource group participation

Key Requirements

  • Bachelor’s degree in relevant engineering field
  • 7 years automation or process engineering experience
  • 7 years industrial Automation System experience
  • 5 years cGMP environment experience
  • 5 years biopharmaceutical process experience
  • Experience with Rockwell Automation, OSIPI, SQL
  • Experience with MES and Trackwise tools

Work Rights

Not specified

Tailored Resume

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