Eli Lilly and Company logo

Engineering Senior Director, Site Expansion

Eli Lilly and Company
On-site
Pleasant Prairie, WI
$147,000 - $215,600 USD yearly
Operations

Role Summary

The Engineering Sr. Director, Site Expansion role is a critical leadership position responsible for guiding the seamless integration of a major site expansion into the siteโ€™s commercial operations. The role focuses on engineering delivery, operational readiness, and alignment with broader project and site objectives.

Responsibilities

  • Deliver engineering support for major expansion project partnering with Lilly Global Project Delivery team to drive efficiency, organizational integration and operational readiness of project integration into the Parenteral manufacturing network
  • Ensure measurement and analytics on key questions, business needs and delivery of key project milestones to help drive the business and better serve our customers
  • Support site annual strategic planning and business plan processes, ensuring project needs including resources are planned and supported
  • Lead and manage operational readiness of major expansion project
  • Building engineering capabilities for site expansion including planning, hiring and onboarding of internal and external resources
  • Partner closely with Engineering leader at the site to ensure alignment between ongoing operations and project needs

Qualifications

  • Required: Bachelorโ€™s degree in engineering
  • Required: 10+ Engineering experience in a parenteral manufacturing site
  • Required: Experience from onboarding and/or executing larger capital projects
  • Required: Previous facility or area start up experience
  • Required: Prior management or leadership experience including leading or working effectively with a cross functional group including network and/or global functions
  • Required: Excellent interpersonal, written, and oral communication skills
  • Required: Strong technical aptitude and ability to train and mentor others
  • Required: Ability to handle multiple competing priorities
  • Preferred: Solid understanding of basic requirements of regulatory agencies
  • Preferred: Previous experience with parenteral engineering/manufacturing
  • Preferred: Previous experience with highly automated equipment
  • Preferred: Previous experience with combination products, device assembly, pharmaceutical packaging, drug product formulation and filling in aseptic environment
  • Preferred: Previous equipment qualification and process validation experience
  • Preferred: Previous experience with Manufacturing Execution Systems and electronic batch release
  • Preferred: Previous experience with Automated Storage and Retrieval System (ASRS) Warehouses or AGVs
  • Preferred: Previous experience with deviation and change management systems including Trackwise