Associate Director - Device, Assembly, And Packaging

Lilly

Indianapolis, Indiana, US
$123,000 - $198,000; bonus eligible; comprehensive...
Operations readiness and startup
Process development and validation
Cross-functional team leadership
The Associate Director is responsible for staffing, training, and leadership of operations groups supporting asset delivery, process development, operations readiness, start up, and validation of parenteral or device, assembly, and packaging areas

Job Summary

  • The Associate Director is responsible for staffing, training, and leadership of operations groups supporting asset delivery, process development, operations readiness, start up, and validation of parenteral or device, assembly, and packaging areas.
  • Key objectives include leading investigations, presenting to regulatory agencies, ensuring operational consistency, and developing strategies for continuous improvement, root cause analysis, and failure modes effect analysis.
  • The role involves managing a workforce of approximately 40-70 individuals, leading cross-functional process teams, and representing the team on the Plant Flow Team, while also providing leadership to deliver business plan goals related to production, finances, safety, quality, and people.

Matching Summary

The Associate Director is responsible for staffing, training, and leadership of operations groups supporting asset delivery, process development, operations readiness, start up, and validation of parenteral or device, assembly, and packaging areas.

Salary

$123,000 - $198,000; Bonus eligible; Comprehensive benefits program

Skills & Requirements

Must-have

  • Operations readiness and startup
  • Process development and validation
  • Cross-functional team leadership
  • cGMP standards and FDA guidelines
  • Continuous Improvement methodologies
  • Stop Work Authority enforcement

Nice-to-have

  • Lean and Six Sigma expertise
  • Automated Storage and Retrieval Systems
  • Employee Resource Groups participation
  • Philanthropy and volunteerism focus

Key Requirements

  • Bachelor's degree in STEM or pharmaceutical field
  • 7+ years in pharmaceutical industry
  • Previous management or leadership experience
  • Understanding of regulatory agencies (FDA, EMEA, DEKRA, OSHA)
  • 4+ years in supervisory role
  • Experience with cGMP standards and FDA guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter