Associate Director - Document & Records Management Process Lead

Eli Lilly UK

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Base: $115,500 - $169,400; bonus/equity: compyny b...
Global quality systems leadership
Documentation and records management
Process standardization and governance
The Associate Director delivers global process leadership, governance, and subject matter expertise to ensure documentation and records management processes are compliant, standardized, and scalable across Research, Development, Manufacturing, and Commercial operations

Job Summary

  • The Associate Director delivers global process leadership, governance, and subject matter expertise to ensure documentation and records management processes are compliant, standardized, and scalable across Research, Development, Manufacturing, and Commercial operations.
  • This role offers a significant opportunity to shape the future state of Lilly’s Documentation and Records Management Process Owner Network while strengthening inspection readiness, documentation quality, and operational execution.
  • Lilly offers a comprehensive benefit program including eligibility for 401(k), pension, medical, dental, vision, flexible benefits, life insurance, and well-being benefits.

Matching Summary

The Associate Director delivers global process leadership, governance, and subject matter expertise to ensure documentation and records management processes are compliant, standardized, and scalable across Research, Development, Manufacturing, and Commercial operations.

Salary

Base: $115,500 - $169,400; Bonus/Equity: Company bonus eligibility depending on performance; Benefits: Comprehensive benefits including 401(k), pension, medical, dental, vision, flexible spending accounts, life insurance, and wellness programs

Skills & Requirements

Must-have

  • global quality systems leadership
  • documentation and records management
  • process standardization and governance
  • inspection readiness and audit preparedness
  • cross-functional stakeholder engagement
  • continuous improvement and analytics
  • project and program management

Nice-to-have

  • enterprise mindset and strategic influence
  • effective communication across all levels
  • leadership of global process owner networks
  • collaboration with IT and analytics teams
  • risk identification and escalation
  • mentoring and development of others

Key Requirements

  • Bachelor’s degree in Life Science-related discipline
  • Experience in pharmaceutical or regulated life sciences industry
  • Experience supporting or leading global quality system initiatives
  • Working knowledge of global regulatory requirements
  • Demonstrated leadership and mentoring experience
  • Ability to travel domestically and internationally

Work Rights

Not specified

Tailored Resume

Cover Letter