Automation Engineer III - BMS/PLC/OEM

Role: Automation Engineer III focusing on GMP manufacturing automation systems at Novartis in Durham, NC, responsible for maintaining, troubleshooting, and optimizing BMS, PLC, OEM, and SCADA systems. Core responsibilities include supporting automation hardware/software lifecycle, integrating third-party equipment, leading automation projects, developing validation and system documentation, executing change controls, and ensuring regulatory compliance aligned with FDA and GMP standards. Requirements: Bachelor's in Engineering, Computer Science, or related field; minimum 5 years' experience in biopharma or 9 years industry equivalent; hands-on experience with DCS platforms (preferably DeltaV), PLC, BMS, SCADA/HMI, automation validation, change controls, and familiarity with OSI PI historian. Preferred skills include strong knowledge of industrial communication protocols, instrumentation, and control architecture, along with excellent cross-functional collaboration skills. High-Value: GMP manufacturing, biopharma automation, regulated environment, validation, FDA compliance, capital project support, and operational reliability. Work setup: onsite role in Durham, NC.