Associate Director - Document & Records Management Process Lead

Lilly

Base: $115,500 - $169,400; bonus/equity: compyny b...
Global quality system governance experience
Regulatory compliance in gxp environments
Leadership of multi-site quality initiatives
This role serves as a P4-level leader accountable for the design, implementation, and sustainment of Lilly's global Documentation and Records Management process across Research, Development, Manufacturing, and Commercial operations

Job Summary

  • This role serves as a P4-level leader accountable for the design, implementation, and sustainment of Lilly's global Documentation and Records Management process across Research, Development, Manufacturing, and Commercial operations.
  • The position requires influencing enterprise-level strategy by chairing global document review boards and maturing a global process forum to ensure inspection readiness and operational execution.
  • Candidates will benefit from a comprehensive compensation package including a base salary between $115,500 and $169,400, company bonuses, and extensive benefits like 401(k) matching and wellness programs.

Matching Summary

This role serves as a P4-level leader accountable for the design, implementation, and sustainment of Lilly's global Documentation and Records Management process across Research, Development, Manufacturing, and Commercial operations.

Salary

Base: $115,500 - $169,400; Bonus/Equity: Company bonus eligible based on performance; Benefits: 401(k), pension, medical/dental/vision, flexible spending accounts

Skills & Requirements

Must-have

  • Global quality system governance experience
  • Regulatory compliance in GxP environments
  • Leadership of multi-site quality initiatives
  • Process standardization and lifecycle management
  • Inspection readiness and audit support

Nice-to-have

  • Data-driven continuous improvement mindset
  • Enterprise-level strategic influence
  • Cross-functional stakeholder collaboration
  • Systems configuration and optimization skills
  • Mentoring and team development capabilities

Key Requirements

  • Bachelor's degree in Business, Science, Engineering, or Pharmacy
  • Experience in pharmaceutical or regulated life sciences industry
  • Proven track record leading global quality system initiatives
  • Working knowledge of global regulatory requirements and inspections

Work Rights

Not specified

Tailored Resume

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