Automation Engineer (3DP)

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.