Lilly is investing over $13 Billion to create a new state-of-the-art manufacturing site for Active Pharmaceutical Ingredient (API) in Lebanon, Indiana. The brand-new facility will focus on peptides and small molecule API manufacturing and will be built using the latest high-tech equipment, advanced highly integrated and automated manufacturing systems, and have a focus on minimizing the impact to our environment. You will be part of the Peptides Process Automation and Control Engineering team responsible for the implementation, support, and optimization of the DeltaV process control system across peptide synthesis and peptide purification. In the project delivery phase and startup phase of the project (startup expected 2027 to 2028), automation engineering roles will be fluid and dynamic as we support the project delivery, build a new organization, develop and implement the necessary systems and business processes required to support GMP operations, and build the site culture. This will require significant collaboration, creativity and resilience as the site grows to a full scale GMP manufacturing through start up.
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Job Type
Full-time
Career Level
Mid Level