Automated Systems Technician — 2nd/3rd Shift (Medical Devices)

The Planet Group

Indianapolis (IN)

On-site

USD 37,000 - 48,000

Full time

14 days+

Get more replies from employers

Send a job-specific resume in minutes.

Benefits offered by this job

3 weeks PTO starting the first year

10 paid holidays

Health/dental/vision benefits starting

401(k) with 50% company match on the 6

Potential annual bonus

Job summary

The Planet Group is seeking an Automated Systems Technician to support highly automated manufacturing lines producing medical drug-delivery devices. You will troubleshoot, maintain, and repair equipment, ensuring compliance with quality and FDA requirements while minimizing downtime on a 2nd or 3rd shift on-site in Indianapolis.

Qualified candidates will have 2+ years in automated environments, strong PLC and robotics experience, and familiarity with Cognex vision systems.

Qualifications

2+ years of experience in an automated manufacturing environment.
Strong PLC experience, preferably Allen Bradley ControlLogix.
Experience with robotics, preferably Fanuc.
Experience with vision systems, preferably Cognex.
Ability to read and understand technical documentation, schematics, and equipment information.

Responsibilities

Troubleshoot and repair highly automated manufacturing equipment to minimize downtime and maintain production schedules.
Identify equipment malfunctions and independently determine appropriate corrective actions.
Work with PLCs, robotics, vision systems, and other programmable automation technologies.
Maintain and troubleshoot Allen Bradley ControlLogix PLCs, Cognex Vision Systems, Fanuc robots, or comparable systems.
Execute preventative maintenance work orders, maintenance protocols, and equipment repairs.
Document all maintenance activities and work performed accurately.
Train on and master automated equipment maintenance procedures and protocols.
Support automated production lines and maintain equipment in a validated state.
Assist Engineering with equipment improvements, testing, process improvements, and cost-reduction initiatives.
Support testing of procedures and documentation required for regulatory compliance.
Maintain customer-specific system documentation in support of FDA requirements.
Write and maintain professional documentation, including protocols, work instructions, and engineering studies.
Manage assigned projects and maintenance activities while meeting aggressive schedules.
Develop the ability to independently support the assigned shift with minimal supervision.
Follow company quality systems, safety procedures, and manufacturing protocols.
Work collaboratively with Engineering, Automation, Maintenance, Quality, and Production teams.