Senior Director - Pr&d Quality Systems

Lilly

Indianapolis, Indiana, US
$156,000 - $228,800; bonus eligibility; comprehens...
Pr&d quality system leadership
Gxp requirements interpretation
Clinical trial manufacturing quality
The PR&D Quality System Sr. Director provides critical technical leadership, leads optimization of the PR&D Quality System to ensure continuous improvement, maintain compliance in a changing regulatory landscape, and network with new R&D facilities for Quality System Integration

Job Summary

  • The PR&D Quality System Sr. Director provides critical technical leadership, leads optimization of the PR&D Quality System to ensure continuous improvement, maintain compliance in a changing regulatory landscape, and network with new R&D facilities for Quality System Integration.
  • Responsibilities include technical leadership of the PR&D Quality System for early phases of clinical manufacturing and supply, interpreting GxP requirements, and influencing the broader PR&D organization regarding quality system changes.
  • Lilly offers a comprehensive benefit program including a company-sponsored 401(k), pension, vacation, medical, dental, vision, and well-being benefits.

Matching Summary

The PR&D Quality System Sr. Director provides critical technical leadership, leads optimization of the PR&D Quality System to ensure continuous improvement, maintain compliance in a changing regulatory landscape, and network with new R&D facilities for Quality System Integration.

Salary

$156,000 - $228,800; Bonus eligibility; Comprehensive benefits package

Skills & Requirements

Must-have

  • PR&D Quality System leadership
  • GxP requirements interpretation
  • Clinical Trial Manufacturing quality
  • Regulatory landscape compliance
  • Continuous improvement initiatives

Nice-to-have

  • Cross-functional problem solving
  • External best practices implementation
  • Proactive senior management influence
  • Quality mindset development
  • Independent and flexible work environment

Key Requirements

  • Bachelor's degree in scientific or medical field
  • 15+ years experience in CGMP manufacturing
  • Experience in Early Phase CT manufacturing
  • Strong working knowledge of cGMP requirements

Work Rights

Not specified

Tailored Resume

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