Scientist - Qa

Eli Lilly

Research Triangle Park, North Carolina, United States
Base: $65,250 - $169,400; bonus/equity: eligible f...
Hybrid
5+ years quality assurance experience
Gmp compliance and regulatory requirements
Non-conformance investigation and root cause analysis
Eli Lilly is seeking a Scientist - QA for their Device Assembly and Packaging team in Research Triangle Park, NC. The role focuses on maintaining GMP compliance and requires extensive experience in Quality Assurance within the pharmaceutical manufacturing sector

Job Summary

  • The Scientist - QA role provides daily oversight and guidance on non-conformance investigations, change controls, and validations to ensure GMP compliance.
  • Lilly is actively growing its manufacturing footprint globally and seeks experienced professionals to support new pioneering technologies at the Research Triangle Park facility.
  • Employees are eligible for a comprehensive benefit program including medical, dental, vision, 401(k), pension, and performance-based bonuses.

Matching Summary

Match Score: 85

Eli Lilly is seeking a Scientist - QA for their Device Assembly and Packaging team in Research Triangle Park, NC. The role focuses on maintaining GMP compliance and requires extensive experience in Quality Assurance within the pharmaceutical manufacturing sector.

Salary

Base: $65,250 - $169,400; Bonus/Equity: Eligible for company bonus based on performance; Benefits: Comprehensive program including 401(k), pension, medical, dental, vision, and wellness benefits

Skills & Requirements

Must-have

  • 5+ years Quality Assurance experience
  • GMP compliance and regulatory requirements
  • Non-conformance investigation and root cause analysis
  • Review of technical studies and validation protocols
  • Cross-functional team collaboration and mentorship

Nice-to-have

  • Experience with highly automated device assembly
  • Knowledge of Manufacturing Execution Systems
  • ASQ certification (CQM, CQE, or CQA)
  • Familiarity with Trackwise, SAP, or Veeva
  • Experience with US/EU regulations and notified bodies

Key Requirements

  • Bachelor's or Master's degree in Engineering or Life Sciences
  • 5+ years of experience in Quality Assurance
  • Strong proficiency with pharmaceutical manufacturing quality systems
  • Demonstrated ability to train and mentor others
  • Strong oral and written communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter