Automation Engineer III

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Able to lift 40 lbs. without assistance, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner, and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

Position will sit onsite at the Florence, SC site and will support the Drug Substance Division (DSD) at Thermo Fisher Scientific. This role, reporting to the Production Planning Manager, ensures the flawless import of materials and goods at our Florence, South Carolina locations.

Work schedule will be standard 8-5, M – F fully onsite

As an Automation Manufacturing Engineer III at Thermo Fisher Scientific, you will optimize production processes, implement new automation technologies, and drive continuous improvement initiatives. You'll work with cross-functional teams to ensure the efficient manufacture of high-quality products while maintaining compliance with regulatory requirements. This position offers the opportunity to contribute meaningfully by enabling our customers to make the world healthier, cleaner and safer through innovative manufacturing solutions.

• You will manage process improvement projects, provide technical automation systems expertise for new product introductions and implement industrial controls and automation systems solutions.
• Working with IT, Quality, Production, and other departments, you'll optimize existing automated processes while ensuring consistent product quality and regulatory compliance.
• Your analytical skills and engineering expertise will help drive cost reductions, improve efficiency, and enhance manufacturing capabilities across our operations.
• Design, configure, and troubleshoot industrial I/O systems, including sensors, actuators, and field instrumentation, ensuring accurate signal mapping and reliable integration with control systems.

• Troubleshooting & Support: Provide rotating on-call (24/7) technical support, troubleshooting, and optimization for manufacturing systems, including but not limited to Allen-Bradley (Rockwell) family products, Emerson DeltaV, Wonder Ware, Honeywell, current DCS, and data historians.
• System Design & Implementation: Contribute to automation and control system design; oversee contractors during implementation, commissioning, and validation of systems (e.g., D3 DCS, Siemens, Allen-Bradley) for both production and utility systems.
• Documentation: Develop, review, and maintain documentation including, but not limited to functional design specifications (FDS), software design documentation, and validation protocols.
• Compliance & Validation: Ensure all systems comply with cGMP, GAMP 5, and FDA regulatory requirements.
• Project Execution: Partner with cross-functional teams (Process Engineering, Operations, Validation, Quality, IT) to execute automation projects, manage vendors, and support system upgrades and lifecycle management.

• Leads multidisciplinary project teams and manages third-party contractors and engineering service providers as required. Supervisory responsibilities and mentorship of less-experienced engineers may be required.

• Bachelor’s degree in Computer Science, Engineering, or a related field required.
• Advanced degree required.

• At least 5 years of experience in manufacturing engineering within regulated industries (pharmaceutical, medical device, or similar) required.
• Hands‑on experience with some of a broad range of Allen‑Bradley PLCs and Panel View display products is preferred.
• Experienc…