Quality Assurance Operations Specialist (night Shift)

Eli Lilly UK

Kenosha County, WI, US
Base: $65,250 - $169,400; bonus/equity: compyny bo...
Fully remote
Gmp compliance and inspection readiness
Batch disposition experience
Quality systems monitoring
The Quality Assurance Operations Specialist is responsible for providing QA oversight to GMP operations occurring on their respective night shift and ensuring inspection readiness

Job Summary

  • The Quality Assurance Operations Specialist is responsible for providing QA oversight to GMP operations occurring on their respective night shift and ensuring inspection readiness.
  • Lilly offers a comprehensive benefits program including 401(k), pension, medical, dental, vision, life insurance, and well-being benefits.
  • The role requires working 12-hour onsite shifts with potential overtime and off-shift support, and includes opportunities to network globally and participate in continuous improvement projects.

Matching Summary

The Quality Assurance Operations Specialist is responsible for providing QA oversight to GMP operations occurring on their respective night shift and ensuring inspection readiness.

Salary

Base: $65,250 - $169,400; Bonus/Equity: Company bonus eligibility based on performance; Benefits: Comprehensive medical, dental, vision, pension, 401(k), life insurance, and wellness programs

Skills & Requirements

Must-have

  • GMP compliance and inspection readiness
  • Batch disposition experience
  • Quality systems monitoring
  • Deviation assessment and triage
  • Change control and validation oversight
  • On-site night shift work
  • Cross-functional collaboration

Nice-to-have

  • Root cause analysis and troubleshooting
  • Technical writing skills
  • Experience with Manufacturing Execution Systems
  • Knowledge of international pharmaceutical regulations
  • ASQ Certification
  • Team mentoring and coaching
  • Continuous improvement participation

Key Requirements

  • Bachelor's degree in science, engineering, or pharmaceutical field
  • Minimum 3 years pharmaceutical industry experience
  • Authorized to work full-time in the United States
  • On-site presence required
  • Experience with batch disposition
  • ASQ Certification

Work Rights

Authorized to work full-time in the United States without sponsorship

Tailored Resume

Cover Letter