Associate Director - Document & Records Management Process Lead

Eli Lilly UK

United Kingdom
Base: $115,500 - $169,400; bonus/equity: compyny b...
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Global process leadership
Quality system design and implementation
Documentation and records management expertise
** Eli Lilly UK is seeking an Associate Director for Document & Records Management, responsible for leading and optimizing global documentation processes within their Quality Systems. The ideal candidate should have a background in the pharmaceutical industry and experience in quality system initiatives, with a focus on compliance and continuous improvement. **

Job Summary

  • This role 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.
  • The Associate Director influences enterprise‑level strategy in one of Lilly’s few truly global process areas and partners closely with senior Quality leadership, QMS governance bodies, and cross‑functional stakeholders.
  • This position 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.

Matching Summary

Match Score: 75

** Eli Lilly UK is seeking an Associate Director for Document & Records Management, responsible for leading and optimizing global documentation processes within their Quality Systems. The ideal candidate should have a background in the pharmaceutical industry and experience in quality system initiatives, with a focus on compliance and continuous improvement. **

Salary

Base: $115,500 - $169,400; Bonus/Equity: Company bonus; Benefits: Comprehensive benefit program

Skills & Requirements

Must-have

  • Global process leadership
  • Quality System design and implementation
  • Documentation and records management expertise
  • Cross-functional stakeholder partnership
  • Inspection readiness support

Nice-to-have

  • Enterprise-level strategy influence
  • Process Owner Network development
  • Data-driven continuous improvement
  • Systems SME for enabling tools

Key Requirements

  • Bachelor’s degree in Business, Physical or Natural Science, Engineering, Pharmacy, or Life Science
  • Experience in pharmaceutical or regulated life sciences industry
  • Experience supporting global quality system initiatives
  • Working knowledge of global regulatory requirements

Work Rights

Not specified

Tailored Resume

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