The ideal candidate will bring strong experience with MES platforms and integrated manufacturing systems, with particular expertise in PAS-X, DeltaV, and SAP within a regulated GMP environment. Key Responsibilities Serve as the MES Subject Matter Expert supporting manufacturing operations and digital manufacturing initiatives. Provide technical leadership for MES configuration, implementation, optimization, troubleshooting, and lifecycle support. Support integration and data flow between PAS-X, DeltaV, SAP, and associated manufacturing systems. Partner with Manufacturing, Automation, Engineering, Quality, IT/OT, and Validation teams to ensure reliable and compliant system performance. Support electronic batch records, master batch record configuration, manufacturing workflows, recipes, and system interfaces. Lead or support system changes, upgrades, testing, commissioning, qualification, and validation activities. Troubleshoot complex MES and system-integration issues and drive root-cause resolution. Ensure solutions comply with GMP, data integrity, computerized system validation, and applicable regulatory requirements. Develop and maintain technical documentation, procedures, specifications, and system lifecycle documentation. Provide technical guidance and mentorship to project and site teams. Qualifications Bachelor's degree in Engineering, Computer Science, Automation, Information Systems, or a related technical discipline. Demonstrated experience supporting MES in pharmaceutical, biotechnology, or other regulated manufacturing environments. Strong hands-on knowledge of Werum/Körber PAS-X. Experience with Emerson DeltaV and SAP integrations in a manufacturing environment. Strong understanding of electronic batch records, manufacturing workflows, automation integration, and production systems. Experience supporting GMP computerized systems, commissioning/qualification, validation, change control, deviations, and system lifecycle activities. Strong troubleshooting, communication, and cross-functional collaboration skills. Experience integrating MES, automation, and enterprise systems in complex pharmaceutical manufacturing environments is highly preferred.