Scientist/engineer - Technical Services/manufacturing Science (filling)

Eli Lilly

Research Triangle Park, North Carolina, USA
Base: $66,000 - $171,600; bonus/equity: compyny bo...
On-site
Parenteral drug product manufacturing
Aseptic processes
Root cause analysis
Eli Lilly is seeking a Scientist/Engineer for their Technical Services/Manufacturing Science team in Research Triangle Park, North Carolina. The role involves providing technical guidance for parenteral operations, particularly in prefilled syringe manufacturing and routine operations, requiring a strong background in engineering or chemistry and experience in cGMP manufacturing

Job Summary

  • The role provides technical guidance for parenteral operations and projects for filling, spanning the design and delivery of prefilled syringe operations as well as support of routine manufacturing.
  • Key responsibilities include performing root cause analysis for manufacturing deviations, providing technical support for technology transfer and process validation, and authoring/reviewing technical documents.
  • The position requires a BS or MS in a related scientific discipline with a minimum of 5 years of experience supporting cGMP manufacturing and involves frequent presence on the production floor.

Matching Summary

Match Score: 85

Eli Lilly is seeking a Scientist/Engineer for their Technical Services/Manufacturing Science team in Research Triangle Park, North Carolina. The role involves providing technical guidance for parenteral operations, particularly in prefilled syringe manufacturing and routine operations, requiring a strong background in engineering or chemistry and experience in cGMP manufacturing.

Salary

Base: $66,000 - $171,600; Bonus/Equity: Company bonus; Benefits: Comprehensive benefit program including 401(k), pension, vacation, medical, dental, vision, prescription drug benefits, flexible benefits, life insurance, time off/leave of absence, and well-being benefits.

Skills & Requirements

Must-have

  • parenteral drug product manufacturing
  • aseptic processes
  • root cause analysis
  • process validation
  • technical documentation
  • cGMP manufacturing support
  • process variability and capability

Nice-to-have

  • cross-functional team collaboration
  • sharing learnings
  • improving process control
  • safety culture participation

Key Requirements

  • BS or MS in Chemical Engineering, Biochemical Engineering, Mechanical Engineering, Chemistry, Biochemistry, or related scientific discipline
  • Minimum 5 years of experience supporting cGMP manufacturing

Work Rights

Not specified

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