Idap Ts/ms Steward

Eli Lilly UK

Indianapolis, Indiana, US
Base: $66,000 - $171,600; bonus/equity: compyny bo...
On-site
Technical leadership across all processes
Maintain validated state of all idap processes
Establish metrics for capability and control
The Technical Services Manufacturing Scientist (TS/MS) Product Steward is responsible for providing technical leadership across all processes and products within the Indianapolis Device Assembly and Packaging (IDAP) site

Job Summary

  • The Technical Services Manufacturing Scientist (TS/MS) Product Steward is responsible for providing technical leadership across all processes and products within the Indianapolis Device Assembly and Packaging (IDAP) site.
  • Primary objectives include maintaining the validated state of all IDAP processes, establishing metrics to ensure a state of capability and control, harmonization of control strategies across process teams, improvement of the processes, and serving as an escalation point for day-to-day operations.
  • The role is also responsible for technical leadership of commercialization activities at the site and is expected to serve as a mentor to other employees within the TS/MS team and other functions within IDAP.

Matching Summary

The Technical Services Manufacturing Scientist (TS/MS) Product Steward is responsible for providing technical leadership across all processes and products within the Indianapolis Device Assembly and Packaging (IDAP) site.

Salary

Base: $66,000 - $171,600; Bonus/Equity: Company bonus (depending on performance); Benefits: Comprehensive benefit program including 401(k), pension, vacation, medical, dental, vision, life insurance, time off, and well-being benefits

Skills & Requirements

Must-have

  • technical leadership across all processes
  • maintain validated state of all IDAP processes
  • establish metrics for capability and control
  • harmonization of control strategies
  • technical leadership of commercialization activities

Nice-to-have

  • mentor to other employees
  • serve as interface with upstream suppliers
  • collaborate with cross-functional teams

Key Requirements

  • Bachelors degree or higher in engineering, science, or related field
  • Clear understanding of cGMPs
  • 5 years of experience in a manufacturing organization
  • Pharmaceutical manufacturing experience
  • Authorized to work in the United States on a full-time basis

Work Rights

Must be authorized to work in the US

Tailored Resume

Cover Letter