Director, Engineering, Parenteral (m2-m3)

Eli Lilly UK

Concord, NC, US
$186,767.00 py; bonus eligible; comprehensive bene...
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Parenteral/dap systems
Automation system experience
Cgmp environment experience
** Eli Lilly is seeking a Director of Engineering for its Parenteral division in Concord, NC, to lead a team responsible for the design and operation of parenteral systems. The ideal candidate will have extensive experience in automation and process engineering within the pharmaceutical industry, particularly in biopharmaceutical processes. **

Job Summary

  • Lead a team of professionals in delivering the full scope of parenteral/DAP systems from user requirements through operation.
  • Achieve business goals related to safety, quality, and process efficiency by maintaining performance metrics and driving improvements.
  • Strategically participate in initiatives like Continuous Improvement, RCA, and FMEA, direct engagement with regulatory agencies, and influence over manufacturing control strategies.

Matching Summary

Match Score: 75

** Eli Lilly is seeking a Director of Engineering for its Parenteral division in Concord, NC, to lead a team responsible for the design and operation of parenteral systems. The ideal candidate will have extensive experience in automation and process engineering within the pharmaceutical industry, particularly in biopharmaceutical processes. **

Salary

$186,767.00 per year; Bonus eligible; Comprehensive benefit program

Skills & Requirements

Must-have

  • Parenteral/DAP systems
  • Automation System experience
  • cGMP environment experience
  • Biopharmaceutical processes and equipment
  • Automated equipment and aseptic processing

Nice-to-have

  • Continuous Improvement initiatives
  • Regulatory agency engagement
  • Manufacturing control strategies influence
  • Diverse, engineering-driven organization

Key Requirements

  • Bachelor's degree in Engineering
  • 7 years of automation or process engineering experience
  • 7 years industrial experience in Automation System
  • 5 years industrial experience in cGMP environment
  • 5 years experience with biopharmaceutical processes and equipment
  • Experience with MES systems and change management tools

Work Rights

Not specified

Tailored Resume

Cover Letter