Join a team where precision meets innovation.
At Cadence, we’re advancing what’s possible in medical device manufacturing — and we’re looking for hands-on, detail-driven Automation Engineering Technicians who thrive in fast-paced, high-tech environments. In this role, you’ll support a cutting-edge, integrated manufacturing cell running 24/7 in a cleanroom setting. Your expertise will keep our automation running at peak performance and directly impact the quality, reliability, and efficiency of life-changing medical devices.
Position Summary
The Automation Engineering Technician is responsible for sustaining and optimizing highly integrated, automated manufacturing cells operating in a 24/7 medical device production environment. This role provides advanced electro-mechanical troubleshooting, PLC diagnostics, equipment maintenance, and continuous improvement support to ensure maximum equipment uptime, product quality, and regulatory compliance.
This position plays a critical role in maintaining validated systems in an ISO-regulated cleanroom environment and directly supports the reliable production of life-saving medical devices.
Key Responsibilities:
Equipment Maintenance & Troubleshooting
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Troubleshoot, diagnose, and repair automated and semi-automated production equipment including robotics, servo systems, pneumatic assemblies, and motion control systems.
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Perform root cause analysis of electrical, mechanical, PLC, and process-related failures; implement corrective and preventive actions.
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Interpret electrical schematics, mechanical drawings, and PLC logic to resolve system faults.
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Maintain and troubleshoot PLC-controlled systems, HMI interfaces, sensors, actuators, VFDs, and safety circuits.
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Perform preventive and predictive maintenance activities to maximize uptime and extend equipment life.
Automation & Process Support
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Support integrated manufacturing cells including assembly, inspection, testing, and grinding operations (CNC and/or manual).
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Monitor cycle times and equipment performance metrics; identify and implement improvements to increase OEE.
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Assist engineers with equipment modifications, upgrades, and continuous improvement initiatives.
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Support validation activities including IQ/OQ/PQ documentation and execution for new or modified equipment.
Installation & Commissioning
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Assist with installation, startup, debugging, and validation of new automation systems.
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Support FAT/SAT activities and coordinate with cross-functional teams during new line launches.
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Ensure equipment changes comply with change control and quality system requirements.
Training & Collaboration
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Train operators and maintenance personnel on equipment operation, troubleshooting, and safety best practices.
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Collaborate closely with Manufacturing Engineering, Quality, and Production teams to resolve technical issues.
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Document maintenance activities, corrective actions, and process changes in compliance with quality standards.
Compliance & Cleanroom Standards
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Perform all work in accordance with ISO 13485, GMP, and cleanroom protocols.
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Ensure adherence to EHS policies, lockout/tagout procedures, and safety standards.
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Maintain accurate maintenance records and support audit readiness.
Required Qualifications
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Associate degree or technical diploma in Electro-Mechanical Technology, Automation, Mechatronics, Industrial Maintenance, or related field — or equivalent hands-on experience.
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Minimum 3 years of experience supporting automated manufacturing equipment in a production environment.
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Demonstrated experience troubleshooting PLC systems (Allen-Bradley, Siemens, or equivalent).
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Strong electrical troubleshooting skills (24V control systems, motors, relays, I/O systems).
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Mechanical aptitude including pneumatics, motion systems, bearings, and mechanical assemblies.
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Ability to read and interpret electrical schematics and mechanical drawings.
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Experience working in regulated manufacturing environments.
Preferred Qualifications
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Experience supporting integrated/custom automation cells.
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CNC or manual grinding experience.
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Experience with robotics and servo-driven systems.
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Background in ISO 13485 medical device manufacturing.
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Cleanroom manufacturing experience.
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Familiarity with validation protocols (IQ/OQ/PQ).
Key Competencies
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Strong analytical and root cause problem-solving skills
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High attention to detail in regulated environments
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Clear technical communication skills
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Ability to work independently in a fast-paced production setting
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Collaborative mindset with cross-functional teams
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Flexibility to support off-shift troubleshooting as required
Why Join Our Team
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Work on advanced, custom-built automation systems in a clean, high-tech environment.
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Play a direct role in manufacturing life-changing medical devices.
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Be part of a culture that values continuous improvement and technical excellence.
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Competitive compensation, comprehensive benefits, and career advancement opportunities.
