Principal Associate Qa - Idm (r3 – R4)

Eli Lilly UK

Indianapolis, IN, US
Base: $124,200.00 py; bonus/equity: compyny bonus ...
Quality oversight for medical devices
Technical transfer to contract manufacturing
Design for manufacturability reviews
Eli Lilly and Company seeks a Principal Associate QA - IDM (R3 – R4) to provide quality oversight and support for medical devices and combination products during technical transfer to contract manufacturing operations

Job Summary

  • Eli Lilly and Company seeks a Principal Associate QA - IDM (R3 – R4) to provide quality oversight and support for medical devices and combination products during technical transfer to contract manufacturing operations.
  • The position requires ensuring design meets critical requirements and risks to product quality have been identified, addressed, and tested, and verifying manufacturing readiness for contract manufacturers and suppliers.
  • Lilly offers a comprehensive benefit program including 401(k), pension, medical, dental, vision, life insurance, and well-being benefits, and is dedicated to equal opportunity and workforce accommodation.

Matching Summary

Eli Lilly and Company seeks a Principal Associate QA - IDM (R3 – R4) to provide quality oversight and support for medical devices and combination products during technical transfer to contract manufacturing operations.

Salary

Base: $124,200.00 per year; Bonus/Equity: Company bonus eligibility; Benefits: Comprehensive benefits including 401(k), pension, medical, dental, vision, life insurance, and well-being benefits

Skills & Requirements

Must-have

  • Quality oversight for medical devices
  • Technical transfer to contract manufacturing
  • Design for manufacturability reviews
  • Experience with plastic molding and assembly
  • Use of Microsoft applications, Veeva, TrackWise

Nice-to-have

  • Supportive employee resource groups
  • Commitment to diversity and inclusion
  • Part-time telecommuting permitted
  • Up to 25% domestic travel

Key Requirements

  • Bachelor’s degree in Chemical or Mechanical Engineering or related field
  • 5 years experience in Quality, Technical Services, Product Development or Manufacturing of medical devices
  • 5 years experience with global medical device regulations
  • 5 years experience with Quality System elements and manufacturing validation
  • 5 years experience with plastic molding/assembly operations
  • 5 years experience with Microsoft applications, Veeva, TrackWise

Work Rights

Not specified

Tailored Resume

Cover Letter