Automation Engineer (3DP) (371)

Réalta Technologies are searching for an Automation Engineer with strong Allen-Bradley PLC and 3D Printing (3DP)/Additive Manufacturing technologies experience to support our Medical Device client based in Raynham, MA, USA.

The ideal candidate will support the development, deployment, and optimisation of automated equipment in a regulated FDA environment. This role requires deep technical capability, strong documentation discipline and the ability to collaborate across Engineering, Quality and Operations.

Job Responsibilities

• Design, program, and troubleshoot automated equipment using Allen-Bradley platforms (ControlLogix, CompactLogix, Studio 5000).
• Lead integration and automation initiatives for 3D Printing/Additive Manufacturing processes, ensuring consistent, validated operation.
• Support equipment installation, commissioning, and qualification activities (IQ/OQ/PQ).
• Develop and maintain technical documentation, including specifications (URS/FDS), design documentation, test protocols, and change controls.
• Improve equipment performance and reliability through data-driven root cause analysis and continuous improvement activities.
• Ensure compliance with FDA 21 CFR Part 820, ISO 13485, GAMP 5, and internal quality system requirements.
• Collaborate with cross-functional teams to troubleshoot manufacturing issues and implement corrective actions.
• Provide ongoing technical support and training to operations and maintenance teams.
• Participate in risk assessments (FMEA), CAPA investigations, and process validation activities.

Job Requirements

• 6+ years of experience in automation engineering within medical devices, pharmaceuticals, aerospace, automotive, or other regulated manufacturing sectors.
• Demonstrated proficiency with Allen-Bradley PLC programming, ladder logic, structured text, and control system architecture.
• Hands-on experience working with 3D printing/additive manufacturing systems, including process automation, integration, and optimisation.
• Strong understanding of industrial communications (EtherNet/IP, DeviceNet, etc.).
• Experience with HMI development (FactoryTalk View or equivalent).
• Solid knowledge of equipment qualification and regulatory compliance in the U.S. medical device industry.
• Excellent analytical, documentation, and communication skills.