Idm Ts/ms Product Steward (r2-r3)

Eli Lilly UK

Indianapolis, IN, US
Base: $101,254.00 py; bonus/equity: compyny bonus ...
Design control and validation activities
Cad software packages expertise
Root cause analysis and corrective actions
Eli Lilly unites caring with discovery to make life better for people around the world and is a global healthcare leader

Job Summary

  • Eli Lilly unites caring with discovery to make life better for people around the world and is a global healthcare leader.
  • The role involves leading root cause investigations, organizing FMEA meetings, and supporting manufacturing objectives through cross-functional collaboration.
  • Lilly offers a comprehensive benefits program including 401(k), pension, medical coverage, and well-being benefits, and is committed to equal opportunity employment.

Matching Summary

Eli Lilly unites caring with discovery to make life better for people around the world and is a global healthcare leader.

Salary

Base: $101,254.00 per year; Bonus/Equity: Company bonus depending on performance; Benefits: Comprehensive benefits including 401(k), pension, medical, dental, vision, life insurance, and well-being programs

Skills & Requirements

Must-have

  • Design control and validation activities
  • CAD software packages expertise
  • Root cause analysis and corrective actions
  • Regulated manufacturing operations environment
  • Failure Modes and Effects Analysis (FMEA)
  • Drug product and medical device regulatory compliance

Nice-to-have

  • Continuous improvement of test systems
  • Multi-functional project team leadership
  • Participation in Design and Manufacturability reviews
  • Support for CMO Joint Process Teams
  • Employee resource group involvement

Key Requirements

  • Bachelor’s degree in Mechanical, Biomedical, Electrical Engineering or related
  • 3 years experience in technical services or manufacturing sciences
  • 3 years experience with CAD software (Solidworks, ProE, Inventor)
  • 3 years experience with GD&T drawing practices
  • 3 years experience in continuous improvement and validation processes
  • 3 years experience with drug product and medical device regulatory standards
  • Up to 10% domestic and international travel

Work Rights

Not specified

Tailored Resume

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