Provide senior automation engineering support across design, integration, programming, testing, commissioning, validation, troubleshooting, and documentation. Support BMS, COPA-DATA Zenon, EMS, PLC, and process automation systems in an active GMP-regulated manufacturing environment. Collaborate with engineering, quality, validation, IT, operations, vendors, and project teams while ensuring compliance with GMP, safety, data integrity, and site procedures.

Lead automation projects for design, implementation, testing, commissioning, validation support, and closeout in a GMP-regulated manufacturing environment. Coordinate system integration, PLC and BMS/Zenon/EMS modifications and migrations, manage schedules, risks, outages, and stakeholder/vendor coordination while ensuring compliance with safety, quality, and site procedures.

Provides process engineering support in regulated pharmaceutical and biotechnology manufacturing environments. Responsibilities include troubleshooting processes and equipment, optimizing performance, supporting capital projects and equipment modifications, developing technical documentation, and participating in commissioning, qualification, validation, change controls, deviations, CAPAs, and risk assessments. The role collaborates with Manufacturing, Quality, Validation, Automation, Maintenance, vendors, and other technical teams while ensuring GMP compliance and advancing continuous improvement initiatives.