Lebanon, Indiana, United States
Key technologies and capabilities for this role
Common questions about this position
The position is full-time employment.
The role is based at Lilly's advanced manufacturing facility in Lebanon, IN.
Responsibilities include maintaining regulatory compliance, executing the production plan, troubleshooting process problems, monitoring equipment, and upholding a safety-first, quality-always mindset.
The culture emphasizes collaboration, creativity, and resilience during the startup phase, with roles being fluid and dynamic as the team builds processes and the organization for GMP operations.
Strong candidates will have experience in API manufacturing, a safety-first and quality mindset, ability to troubleshoot processes, and resilience to thrive in a dynamic startup environment for a greenfield GMP site.
Develops and delivers prescription medicines globally
Eli Lilly and Company is a global pharmaceutical company that focuses on discovering, developing, and delivering medicines to improve health. The company has a long history of scientific achievements, including the creation of insulin, the first life-saving treatment for diabetes. Lilly's operations involve extensive research and development to create new medications and enhance existing ones, ensuring they are safe and effective. Their products are primarily prescription medicines sold to healthcare providers for various medical conditions, including diabetes, cancer, and pain management. What sets Lilly apart from its competitors is its strong commitment to ethical practices and the protection of its products from counterfeiting. The company's goal is to enhance lives through innovative medical solutions while maintaining high standards of quality and ethics.