Associate Director - Project Management Office (pmo)

Eli Lilly

Kenosha, Wisconsin, United States
Base: $123,000 - $180,400; bonus/equity: compyny b...
Hybrid
12 years pharmaceutical manufacturing experience
Pmp or pgmp certification required
Fda, ema, and gxp regulatory knowledge
Eli Lilly is seeking an Associate Director for their Project Management Office (PMO) in Kenosha, Wisconsin, to lead project management initiatives, ensure adherence to industry regulations, and foster a culture of accountability. The ideal candidate will possess extensive experience in pharmaceutical manufacturing and project management, along with leadership capabilities to mentor and develop a team

Job Summary

  • The role involves leading a team of project managers to drive consistency and execution across the site project portfolio.
  • Candidates must ensure all projects adhere to strict industry regulations including FDA, EMA, and GxP standards.
  • Eli Lilly offers a comprehensive benefit program including medical, dental, vision, 401(k), and wellness benefits.

Matching Summary

Match Score: 85

Eli Lilly is seeking an Associate Director for their Project Management Office (PMO) in Kenosha, Wisconsin, to lead project management initiatives, ensure adherence to industry regulations, and foster a culture of accountability. The ideal candidate will possess extensive experience in pharmaceutical manufacturing and project management, along with leadership capabilities to mentor and develop a team.

Salary

Base: $123,000 - $180,400; Bonus/Equity: Company bonus depending on performance; Benefits: Comprehensive program including 401(k), pension, medical, dental, vision, and wellness

Skills & Requirements

Must-have

  • 12 years pharmaceutical manufacturing experience
  • PMP or PgMP certification required
  • FDA, EMA, and GxP regulatory knowledge
  • Team leadership of project managers
  • Budget and resource allocation management
  • Microsoft Project and SmartSheet proficiency

Nice-to-have

  • MBA or Master's degree in Project Management
  • Experience with Clinical Research Organizations
  • Strong learning agility and flexibility
  • Cross-functional collaboration skills
  • Hybrid work model availability

Key Requirements

  • Bachelor's degree in Science, Engineering, Business, or related field
  • 12 years of progressive experience in pharmaceutical manufacturing
  • PMP Certified or similar certifications (PgMP, PfMP)
  • Proven experience as a leader of a Project Management Team

Work Rights

Not specified

Tailored Resume

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