At cGMP Consulting, we specialize in providing expert validation, qualification, and compliance services to the life sciences industry. Our team works with clients to ensure their facilities, equipment, and processes meet regulatory standards, enabling the safe and efficient production of pharmaceuticals. cGMP Consulting is based in Lake Forest, IL. Our main client locations are Melrose Park, IL, North Chicago, IL, Waukegan, IL and Pleasant Prairie, WI. Position Summary cGMP Consulting is seeking an experienced MES Engineer to support manufacturing production activities. They will support projects that improve manufacturing efficiency and safety, decrease costs, decrease opportunity for human error, or increase compliance. This individual will use POMS, SAP, and other systems, programs, and databases to input, verify, monitor, and analyze pertinent data. They will be able to identify opportunities for improvement of manufacturing and business processes. They will propose, plan and facilitate the improvement solutions and are responsible for production metrics, standards, and reporting on a weekly basis. This role requires excellent analytical abilities, the ability to understand complex solutions and processes, and a strong focus on driving data quality improvements. This candidate will work cross-functionally with local and global teams in a GMP-compliant manufacturing environment.