Job ResponsibilitiesSpearhead the design, implementation, and maintenance of process control systems.Independently execute control system upgrades and capital projects, adhering to engineering best practices.Sustain and enhance automation systems through preventive maintenance, troubleshooting, system expansions, and user management.Review and revise engineering standards to align with industry advancements.Foster a safe and compliant workplace by following safety protocols and standard operating procedures.Support manufacturing operations with equipment upgrades, new installations, and troubleshooting assistance.Facilitate rapid restoration of equipment functionality to reduce downtime.Contribute to capital budget planning by identifying system improvement needs and service requirements.Estimate project budgets, including costs for labor, materials, and external services.Ensure adherence to U.S. and international regulatory standards, including FDA, EU, Health Canada, TGA, PIC/S, ISO, USP, NRC, and cGMP.Perform on-site inspections during the installation and implementation of automation hardware and systems.Undertake additional duties as assigned, with or without accommodation.QualificationsBachelor’s in Engineering or related field.8+ years in manufacturing automation; 5+ years preferred in regulated industries (e.g., FDA).Strong background in pharma capital projects and cross-functional team collaboration.Skilled in PLC (Allen Bradley, Siemens), HMI, robotics (Staubli), motor controls, vision systems (Cognex), and sensors.Proficient in commissioning, debugging, validation, and process control.Excellent communication, organization, and multitasking under pressure.Preferred: Knowledge of power distribution, BMS, alarms, communication protocols, SQL, web reporting, and validation systems.Project management experience a plus.Strong problem-solving and adaptable to shifting priorities.Proficient with Microsoft Office.