Eli Lilly and Company logo

Associate Director - Operational Readiness

Eli Lilly and Company
Full-time
Remote friendly (Houston, TX)
United States
Operations

Want to see how your resume matches up to this job? A free trial of our JobsAI will help! With over 2,000 biopharma executives loving it, we think you will too! Try it now β€” JobsAI.

Role Summary

The Associate Director β€šΓ„Γ¬ Operational Readiness is a key site leader responsible for developing and managing an integrated project plan to prepare the manufacturing facility for operational readiness. This role leads the siteβ€šΓ„Γ΄s Operational Excellence group, establishing Lean principles and a continuous improvement framework, to ensure a safe, timely, and successful startup of GMP manufacturing operations.

Responsibilities

  • Identify essential pre-manufacturing elements for facility readiness with input from cross-functional stakeholders.
  • Collaborate with the GFD project team and site functions to develop an integrated startup plan, addressing dependencies, timelines, and resource needs.
  • Serve as the main liaison between the GFD project and site teams to ensure clear communication and aligned priorities.
  • Lead a cross-functional team to implement the plan, foster collaboration, and build team morale.
  • Align scope, goals, and timelines with stakeholders to meet project objectives.
  • Drive timely decision-making under tight deadlines.
  • Manage communications and relationships with internal and external stakeholders.
  • Proactively resolve issues and implement corrective actions.
  • Forecast and manage resource needs to avoid project delays.
  • Report key metrics to site and network governance forums.
  • Apply lean management practices to streamline meetings, communication, and escalation.
  • Build a culture of operational excellence and embed Lean principles into site governance.

Qualifications

  • Bachelor's degree in a relevant discipline (STEM degree preferred) and experience in a functional or operational leadership role within the pharmaceutical industry.
  • 5+ years of experience supporting GMP operations

Additional Preferences

  • Proven experience leading large, cross-functional projects from initiation to successful delivery
  • Ability to thrive in dynamic environments and adapt quickly to shifting priorities
  • Skilled in influencing decisions on complex technical challenges
  • Strong organizational and self-management skills; able to prioritize and adjust workload effectively
  • Effective collaboration across diverse functions (e.g., Technical Services, Engineering, Quality, QC, IT, Operations) with ability to integrate workstreams
  • Demonstrated ability to influence peers and business partners
  • Strong interpersonal and team-building skills; fosters effective collaboration among diverse styles
  • Track record of delivering high-performance projects on time and within budget
  • Proficient in continuous improvement methodologies (Lean, Six Sigma, etc.)
  • Familiarity with documentation, deviation, and change management systems (e.g., TrackWise, Veeva, QualityDocs, Kneat)
Apply now
Share this job