Principal Assembly Process Engineer

Eli Lilly and Company

Indianapolis, Indiana, US
$126,000 - $204,600; bonus/equity: compyny bonus; ...
Hybrid
Assembly process development
Medical device manufacturing
Combination product assembly
The Principal Assembly Process Engineer serves as a senior technical authority and process development leader within the DDCS Embedded Systems and Process Engineering (ESPE) group, accountable for building and advancing assembly process engineering capabilities across Lilly’s drug delivery device portfolio

Job Summary

  • The Principal Assembly Process Engineer serves as a senior technical authority and process development leader within the DDCS Embedded Systems and Process Engineering (ESPE) group, accountable for building and advancing assembly process engineering capabilities across Lilly’s drug delivery device portfolio.
  • Responsibilities include leading design, development, and optimization of assembly processes, establishing engineering best practices, and guiding cross-functional teams through the design, development, and scale-up of automated and semi-automated assembly processes.
  • Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance), and Lilly offers a comprehensive benefit program including 401(k), pension, vacation, medical, dental, vision, and more.

Matching Summary

The Principal Assembly Process Engineer serves as a senior technical authority and process development leader within the DDCS Embedded Systems and Process Engineering (ESPE) group, accountable for building and advancing assembly process engineering capabilities across Lilly’s drug delivery device portfolio.

Salary

$126,000 - $204,600; Bonus/Equity: Company bonus; Benefits: Comprehensive benefit program

Skills & Requirements

Must-have

  • Assembly process development
  • Medical device manufacturing
  • Combination product assembly
  • Automated assembly systems
  • Process FMEA
  • Risk management frameworks

Nice-to-have

  • Digital health devices
  • Industry 4.0 concepts
  • Statistical rigor
  • Cross-functional team leadership
  • External professional organizations engagement

Key Requirements

  • Bachelor of Science in Engineering
  • 10+ years of experience
  • Process/equipment commissioning, qualification, validation (CQV)
  • FDA 21 CFR Part 820 Design Controls
  • ISO 13485 quality management systems

Work Rights

Not specified

Tailored Resume

Cover Letter