Senior Engineering Lead

7 days ago


Marquand, Missouri, United States Eli Lilly Full time
About Eli Lilly

Eli Lilly is a global healthcare leader committed to making life better for people around the world. We unite caring with discovery to develop life-changing medicines, improve disease management, and give back to our communities through philanthropy and volunteerism.

Job Description

We are seeking a highly skilled Senior Principal Engineer to join our Device and Packaging Manufacturing division. This role will provide technical oversight and support for automated assembly processes, ensuring the reliable supply of products across our site. As a key member of our team, you will be responsible for technical aspects of quality, direct impact systems, and critical components used in production, testing, packaging, labeling, and storing of manufactured products.

Key Objectives and Deliverables:
  • Demonstrate ownership of equipment and packaging areas by being flexible, proactive, and involved. Serve as a responsible engineer for site process lines, possessing deep knowledge of equipment and unit operation design characteristics and capabilities on assembly and packaging lines.
  • Ensure equipment is maintained in its qualified state (AQM). Approve scope of qualification and monitoring activities. Review and/or approve significant changes, maintenance, and other interventions for potential adverse impact on safety or quality integrity of equipment or process.

This role offers opportunities for innovation and problem-solving, with responsibilities including:

  • Providing equipment and processing support for production issue resolution and investigation, ensuring reliable solutions, safe execution, and regulatory compliance.
  • Identifying and driving improvement opportunities. Supporting sites with complex investigations of key safety, quality, and production issues, working on identification and implementation of CAPA plans to address such events and prevent recurrence.

The ideal candidate will have 8+ years' experience in pharmaceutical manufacturing or regulated industry, with in-depth knowledge of GMPs, risk management, and process/equipment commissioning and qualification practices. A strong technical leadership and communication skillset, combined with analytical and problem-solving abilities, is essential for success in this role.



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