Process Engineer – Device Assembly

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.  Lilly is a fortune 500 company in operation for 150 years creating high-quality medicines for our patients. The new facility at the Kenosha County campus will be one of Lilly’s most technically advanced manufacturing sites. The facility will include high-speed manufacturing, robotics, advanced data collection and analytics that will result in safety improvements, increased productivity, and variability reduction for Device Assembly lines.   This is an exciting opportunity to help build a state-of-the-art facility and Quality System from the ground up.

As the  Process Engineer – Device Assembly, you will be supporting and managing the Device Assembly crucial to Lilly's supply chain. This role will be part of the LKC Site Engineering organization responsible for the delivery of the lines and support of continuous operations by providing subject matter expertise in process control, improvements, project management, and technical leadership to the process team. This position will require the development of expertise in production processes, commissioning, qualification, and validation requirements and equipment specific code and/or control system technologies. Individuals who have passion to integrate, qualify, and start up complex Device Assembly systems while serving as the technical bridge between OEM equipment, manufacturing control systems, MES, warehouse systems, and site operations are encouraged to apply. Key Objectives/Deliverables: Partner with Corporate Automation, Global Packaging & Robotics, Automation Integrators, and Global Facilities Delivery to design, install, and qualify the new LKC Device Assembly lines. Take overall responsibility for the safe design and safe operation of the equipment within the area. Lead or participate in qualification activities (including commissioning activities of new equipment or areas). Assist in the integration of these lines into the site data collection and SCADA layer. Lead activities through the full project lifecycle including design review, FAT, installation, SAT, qualification, and startup support. Assist for integration between Device Assembly equipment and enterprise manufacturing systems including MES, warehouse management systems, scheduling systems, and site automation platforms. Review OEM electrical, controls, and safety designs to ensure compliance with Lilly standards and applicable industry standards (e.g., machine safety, electrical safety, and control panel requirements). Assist automation verification and qualification activities, including IV/OV testing, system integration testing, and startup troubleshooting. Support implementation and lifecycle management of Lilly manufacturing platforms such as Global Packaging Platform (GPP), GRIP, GPM, Global Scheduler, and MES integrations. Support manufacturing system interfaces including PLCs, HMI/SCADA systems, databases, servers, virtual environments, networks, and middleware platforms. Partner with Quality, Operations, Engineering, IT, OEMs, and global platform teams to resolve complex automation and integration challenges during project execution and commercial operations. Assist manufacturing system startup readiness activities including PSSR execution, safety verification, automation cutovers, and qualification support. Communicate