Associate Director / Director - Global Medicines Quality Organization

Eli Lilly UK

Indianapolis, Indiana, US
Base: $123,000 - $180,400; bonus/equity: compyny b...
On-site
Global medicines quality organization
Gcp regulations/expectations
Quality system compliance
The purpose of the Associate Director / Director, Global Medicines Quality Organization (GMQO) role is to maintain, develop, and improve quality system compliance and enhance quality by partnering with assigned portfolio/function(s)

Job Summary

  • The purpose of the Associate Director / Director, Global Medicines Quality Organization (GMQO) role is to maintain, develop, and improve quality system compliance and enhance quality by partnering with assigned portfolio/function(s).
  • This position leads GMQO associates responsible for supporting the execution and delivery of submissions to global health authorities, using technical expertise and strong knowledge of internal procedures and external GCP regulations.
  • Primary responsibilities include leadership and resource management, quality system implementation, audit and inspection readiness, quality project management, and process improvement.

Matching Summary

The purpose of the Associate Director / Director, Global Medicines Quality Organization (GMQO) role is to maintain, develop, and improve quality system compliance and enhance quality by partnering with assigned portfolio/function(s).

Salary

Base: $123,000 - $180,400; Bonus/Equity: Company bonus; Benefits: Comprehensive benefit program including 401(k), pension, vacation, medical, dental, vision, life insurance, and well-being benefits

Skills & Requirements

Must-have

  • Global Medicines Quality Organization
  • GCP regulations/expectations
  • quality system compliance
  • audit and inspection readiness
  • clinical development quality

Nice-to-have

  • strategic input
  • results-focused
  • critical thinking
  • team collaboration
  • innovation and inclusivity

Key Requirements

  • Bachelor’s Degree in a health-related or scientific field
  • Experience in clinical development
  • Strong knowledge of GCP guidelines and regulations
  • Supervisory experience
  • Experience working in a global environment
  • Demonstrated project management experience

Work Rights

Not specified

Tailored Resume

Cover Letter