Sr. Director - Api Manufacturing Quality Assurance

Lilly

Base: $156,000 - $228,800; bonus: compyny bonus ba...
Not specified
10+ years pharmaceutical manufacturing quality experience
5+ years supervision leadership experience
Cgmp standards compliance expertise
Lilly is seeking a Sr. Director of API Manufacturing Quality Assurance to lead the quality assurance efforts at a new advanced manufacturing facility. The role involves overseeing compliance with cGMP standards, managing quality systems, and leading a team dedicated to ensuring the successful startup of the site

Job Summary

  • The Sr. Director – QA serves as the Site Quality Leader overseeing manufacturing, utilities, laboratories, and warehousing for a new Lilly API site.
  • This role ensures continuous improvement of all quality systems while maintaining cGMP standards for raw materials and drug substances.
  • Lilly offers a comprehensive benefit program including medical, dental, vision, 401(k), pension, and a company bonus depending on performance.

Matching Summary

Match Score: 85

Lilly is seeking a Sr. Director of API Manufacturing Quality Assurance to lead the quality assurance efforts at a new advanced manufacturing facility. The role involves overseeing compliance with cGMP standards, managing quality systems, and leading a team dedicated to ensuring the successful startup of the site.

Salary

Base: $156,000 - $228,800; Bonus: Company bonus based on performance; Benefits: Medical, dental, vision, 401(k), pension, vacation

Skills & Requirements

Must-have

  • 10+ years pharmaceutical manufacturing quality experience
  • 5+ years supervision leadership experience
  • cGMP standards compliance expertise
  • API manufacturing facility knowledge
  • Regulatory inspection coordination skills

Nice-to-have

  • Experience in Development or Technical Services
  • Strong statistical analysis proficiency
  • Ability to influence diverse teams
  • Demonstrated problem-solving analytical thinking
  • Greenfield site startup experience

Key Requirements

  • Bachelor's degree (STEM preferred)
  • 10+ years pharmaceutical manufacturing quality experience
  • 5+ years supervision/leadership experience

Work Rights

Not specified

Tailored Resume

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