Associate Director, Global Manufacturing & Supply

Eli Lilly and Company; Lebanon (IN); On-site; USD 117,000 - 172,000; Full time

Benefits offered by this job

401(k) plan

Pension

Vacation benefits

Medical, dental, vision benefits

Flexible benefits

Life insurance

Job summary

Eli Lilly and Company in Lebanon, Indiana, is initiating a startup phase for a greenfield manufacturing site focused on external manufacturing. The LP2-EM team leader will drive cross-functional collaboration with contract manufacturers and internal teams to align quality, supply plans, and technical agendas for both clinical and commercial supply.

You will manage product supply, schedules, and key metrics while ensuring regulatory compliance and strong internal/external relationships, with

Qualifications

• Bachelor’s degree or equivalent in Chemical Engineering, Mechanical Engineering, Chemistry/Biochemistry or related science.
• 5+ years of experience in pharmaceutical manufacturing, technical support, quality assurance, and/or quality engineering.

Responsibilities

• Lead cross-functional Joint Process Team (JPT) between Lilly and CM to develop and implement quality, supply, and technical agendas.
• Facilitate and ensure GMP compliance to maintain continuous supply.
• Manage production, batch release and shipment schedules to meet objectives.
• Visit CM sites to strengthen operations and relationships; resolve issues with the Lilly/CM Steering Team.

Skills

Leadership

Cross-functional collaboration

Project management

Communication

Adaptability

Education

Bachelor’s degree in Chemical Engineering, Mechanical Engineering, Chemistry/Biochemistry or related science

Tools

Trackwise

SAP

Veeva Vault

Microsoft Project

Job description

Eli Lilly and Company in Lebanon, Indiana, is initiating a startup phase for a greenfield manufacturing site focused on external manufacturing. The LP2-EM team leader will drive cross-functional collaboration with contract manufacturers and internal teams to align quality, supply plans, and technical agendas for both clinical and commercial supply.

You will manage product supply, schedules, and key metrics while ensuring regulatory compliance and strong internal/external relationships, with