Sr. Automation Engineer - Upstream/Media

Novartis•Durham, NC

10d•Onsite

About The Position

Ready to help power the next generation of life-changing therapies? As a Sr. Automation Engineer - Upstream/Media, you will play a critical role in supporting the automation systems that drive upstream manufacturing and media preparation operations. You'll serve as a technical leader within a GMP environment, partnering with cross-functional teams to optimize process performance, enhance system reliability, and deliver automation solutions that enable consistent, compliant production. This is an exciting opportunity to combine technical expertise, innovation, and project leadership while helping shape the future of advanced biopharmaceutical manufacturing.

Requirements

Bachelor's degree in Engineering, Computer Science, or a related technical discipline.
8+ years of automation experience within GMP pharmaceutical or biopharmaceutical manufacturing environments.
Hands-on experience supporting DCS platforms, preferably Emerson DeltaV.
Proven expertise with PLC, SCADA, HMI, and manufacturing automation systems.
Strong knowledge of validation practices, GMP regulations, FDA requirements, and 21 CFR Part 11.
Experience applying ISA-88 principles and developing automation standards within regulated environments.
Demonstrated project leadership experience, including management of contractors and external partners.
Strong troubleshooting, communication, and technical writing skills with the ability to solve complex challenges.

Nice To Haves

Business Continuity
Cost Management
Decision Making
Operational Excellence
Problem Solving
Project Management
Quality Compliance
Risk Management
Stakeholder Management
Vendor Management

Responsibilities

Lead automation support for upstream manufacturing and media process control systems.
Serve as the technical SME for DCS, BMS, MES, and associated control systems.
Drive automation project execution from concept through implementation and operational handoff.
Oversee integration of third-party equipment into site automation and manufacturing platforms.
Develop URS, FS, and design specifications to support compliant system delivery.
Collaborate with cross-functional teams to establish priorities, timelines, and project objectives.
Support new product introductions and upstream process implementation within GMP manufacturing.
Investigate automation-related non-conformances and implement effective corrective actions.
Execute change controls, system upgrades, and continuous improvement initiatives.
Provide technical support for manufacturing operations, including participation in on-call rotations.