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The Systems Engineer will design, develop, and maintain MES software applications, ensuring compliance and optimizing manufacturing processes. Responsibilities include troubleshooting, testing, and driving continuous improvement.

The Senior Manager of Engineering leads efforts in asset delivery, process engineering, and validation of the Parenteral/DAP area, focusing on safety and efficiency.

The Principal Associate QA leads quality oversight in laboratory operations, ensuring compliance with cGMP practices and guiding projects during site startup and daily operations.

As an Automation Engineer, you will design and oversee automation for Lilly's new Concord facility, manage system integrators, and support corporate initiatives.

The Director of Engineering will lead a team to manage parenteral systems from design to operation, focusing on safety, quality, and efficiency, while driving continuous improvement and regulatory compliance.

The Process Engineer will ensure a safe working environment, improve safety culture, and lead troubleshooting efforts in pharmaceutical manufacturing processes showing technical expertise and oversight.

The Sr. Director HSE will lead health, safety, and environmental functions, ensuring compliance, developing systems, and promoting safety at the Concord site.

The Associate Director leads the Technical Services/Manufacturing Science group, overseeing staffing, training, and operational support for manufacturing, ensuring safety and quality while driving continuous improvement initiatives.

The role oversees implementation of contamination control strategies in API manufacturing, influences compliance with regulatory expectations, and provides technical support in new product commercialization and site expansions.

The Automation Engineer will oversee the automation systems for Lilly's new manufacturing facility, manage integration processes, and support technology innovation while ensuring safety and compliance standards are met.