Sr. Automation Engineer - Downstream/Buffer
Novartis
October 2, 2026
Full-time
On-site
Durham, NC
Operations
Role: Senior Automation Engineer supporting downstream/buffer manufacturing operations in a GMP biopharmaceutical setting, with a focus on automation systems for reliable, compliant production. Responsibilities include leading automation system design, configuration, lifecycle management, and project execution; acting as SME for DCS, BMS, MES; supporting system integrations, validation, and continuous improvement initiatives; and providing technical manufacturing support. Requirements: Bachelor's in Engineering, Computer Science, or related; 8+ years in GMP pharma/biopharma automation; hands-on experience with DCS platforms (preferably Emerson DeltaV), PLC, SCADA, HMI; strong knowledge of GMP regulations, validation, and 21 CFR Part 11; proven project leadership including managing contractors. Preferred: experience applying ISA-88 standards and supporting automation standards within regulated environments. High-Value: expertise in automation in biologics or small molecule manufacturing, GMP compliance, validation, and cross-functional project collaboration. Work Setup: onsite in Durham, NC; no relocation support; travel not specified.