Lilly is building a state-of-the-art manufacturing facility dedicated to advanced therapies, leveraging next-generation technologies and analytics to improve safety, quality, and process performance
Job Summary
Lilly is building a state-of-the-art manufacturing facility dedicated to advanced therapies, leveraging next-generation technologies and analytics to improve safety, quality, and process performance.
The Associate Director role involves leading technology transfer, process validation, and ensuring GMP compliance while supporting clinical and commercial supply for gene therapy products.
Employees receive a comprehensive benefits package including eligibility for bonuses, 401(k), pension, medical and dental benefits, and participate in strong employee resource groups supporting diversity and inclusion.
Matching Summary
Lilly is building a state-of-the-art manufacturing facility dedicated to advanced therapies, leveraging next-generation technologies and analytics to improve safety, quality, and process performance.
Salary
Base: $123,000 - $180,400; Bonus/Equity: Company bonus based on performance; Benefits: Comprehensive benefits including 401(k), pension, medical, dental, vision, and wellness programs
Skills & Requirements
Must-have
cGMP commercial manufacturing experience
technology transfer and process validation
gene therapy manufacturing knowledge
cross-functional team collaboration
GMP compliance and documentation oversight
technical leadership and team management
Nice-to-have
experience with AAV and mRNA/LNP manufacturing
strong project management skills
strategic mindset and technical governance
effective communication and influencing skills
rapid technical knowledge application
experience in advanced therapies manufacturing
Key Requirements
BS/MS in Biochemistry, Biotechnology, or related field
5+ years cGMP commercial manufacturing experience
3+ years experience leading teams
knowledge of global regulatory manufacturing expectations