Sr. Automation Engineer – DeltaV

Novartis•Durham, NC

9d•Onsite

About The Position

Novartis is seeking a Sr. Automation Engineer – DeltaV to serve as a technical expert supporting and optimizing critical automation systems in a GMP-regulated manufacturing environment. The role is based onsite in Durham, North Carolina; relocation support is not available. The engineer will lead automation initiatives, improve system reliability and performance, and work with cross-functional teams to support operational excellence and the manufacture of innovative medicines.

Requirements

Bachelor's degree in Engineering, Computer Science, Automation, or a related technical field with at least 8 years of experience supporting GMP pharmaceutical or biopharmaceutical manufacturing operations, or equivalent experience.
Strong hands-on experience programming, troubleshooting, and maintaining DeltaV DCS automation systems.
Experience supporting SCADA, HMI, PLC, BMS, and manufacturing automation platforms in a regulated environment.
Knowledge of GMP, FDA, and 21 CFR Part 11 requirements for manufacturing automation systems.
Experience with automation system validation, qualification, and lifecycle management within GMP operations.
Ability to lead automation projects, execute complex change controls, and drive continuous improvement initiatives.
Experience developing automation documentation, technical specifications, and test protocols.
Strong communication and collaboration skills, including experience partnering across Engineering, Manufacturing, Quality, Validation, and IT teams.

Responsibilities

Serve as a DeltaV subject matter expert, providing technical expertise for automation systems supporting GMP manufacturing operations.
Design, configure, troubleshoot, and optimize DeltaV control strategies and system performance.
Support the full automation system lifecycle, including implementation, upgrades, maintenance, and retirement.
Lead automation projects from concept through commissioning, qualification, and operational handover.
Partner with Manufacturing, Engineering, Quality, Validation, and IT teams to deliver automation solutions.
Drive continuous improvement initiatives to enhance system reliability, efficiency, and product quality.
Investigate automation deviations, implement corrective actions, and support CAPA activities.
Develop and maintain automation documentation, including specifications, test protocols, and system drawings.
Ensure automation systems remain compliant with GMP, FDA, and data integrity requirements.
Provide technical mentorship and subject matter expertise for DeltaV and site automation technologies.