Role Overview
As a PLC Automation Engineer, you will be responsible for developing, implementing, and maintaining automation solutions across manufacturing equipment and processes. You will collaborate with cross-functional engineering, quality, and operations teams to ensure reliable, compliant, and efficient production of medical devices.
Key Responsibilities
Design, program, and troubleshoot PLC-based control systems (Siemens, Allen-Bradley, etc.) for automated equipment.
Support installation, validation and commissioning of new automated systems.
Develop HMI/SCADA systems for operator-friendly interfaces.
Ensure compliance with FDA, ISO 13485, and GxP standards in all automation activities.
Collaborate with Manufacturing Engineering, Quality, and Maintenance teams to improve reliability and efficiency.
Conduct root cause analysis and resolve automation-related issues with minimal downtime.
Manage preventive and predictive maintenance strategies for control systems.
Document software, configuration changes, and validation protocols as per regulatory requirements.
Support continuous improvement projects (Lean, Six Sigma, Industry 4.0) with automation solutions.
Train technicians and operators on equipment functionality and safety protocols.
Qualifications & Skills
Bachelor’s Degree in Electrical / Electronics / Mechatronics / Automation Engineering (or related field).
5-7 years of experience in PLC automation engineering, preferably in the MedTech, Pharma, or High-Tech Manufacturing sector.
Hands-on experience with PLC programming (Siemens S7, Allen-Bradley, Omron, etc.) and HMI development.
Knowledge of industrial networks (Ethernet/IP, Profibus, Profinet, Modbus).
Strong understanding of machine safety (LOTO, CE, ISO 13849-1, EN 60204-1).
Excellent troubleshooting, problem-solving, and analytical skills.
Ability to work cross-functionally in a fast-paced manufacturing environment.
Good communication and documentation skills.
Preferred Skills (Nice To Have)
Experience with robotics, vision systems.
Familiarity with 21 CFR Part 11 compliance for electronic records.
Exposure to MES (Manufacturing Execution Systems) and Industry 4.0 technologies.
Lean Six Sigma Green Belt or equivalent certification.
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