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Controls Engineer

Job in Jacksonville, Duval County, Florida, 32290, USA
Listing for: Medical Engineering Consultants (MEC)
Full Time position
Listed on 2025-12-03
Job specializations:
  • Engineering
    Electrical Engineering, Manufacturing Engineer
Job Description & How to Apply Below

Controls Engineer – Contract

Medical Engineering Consultants (MEC) support medical device and pharmaceutical companies by providing resources and expertise. Our vision is to align client needs with the best marketplace resources and drive sustainable improvement.

Key Responsibilities
  • Create, develop, and implement control systems for automated manufacturing equipment, including PLCs, HMIs, and motion control systems.
  • Identify and resolve issues, downtime, and quality problems in automated machinery to optimize safety and efficiency.
  • Ensure all automation and control systems comply with FDA regulations, ISO standards, and GMP requirements specific to medical devices.
  • Develop and maintain technical documentation for control systems, support equipment validation activities, and ensure change control processes are followed.
  • Implement new technologies, conduct root cause analysis for failures, and lead initiatives to enhance reliability and efficiency of manufacturing processes.
  • Support commissioning and upgrades of manufacturing equipment, providing technical support, and training to maintenance teams.
Education and Qualification

A Bachelor's degree in Electrical Engineering, Mechanical Engineering, Manufacturing Engineering, or a related technical field.

Required

Skills and Qualifications
  • Proficiency in PLC programming (e.g., Allen Bradley Control Logix, Siemens), HMI development, motion control, and robotics.
  • Experience with industrial controls, sensors, VFDs, safety hardware, and various automation technologies.
  • Strong analytical and troubleshooting skills to diagnose and resolve complex control system issues.
  • Excellent verbal and written communication skills to collaborate with teams and document technical information.
  • Understanding of the strict regulatory environment for medical device manufacturing, including FDA and GMP.
Duration

Project will start in January 2026 on the 2GT lines 02 and 03, and in Q3‑Q4 2027 will support a new packaging project in the Repack lines. The role is 1 year.

Additional Information

MEC does not accept unsolicited resumes through search firms or staffing agencies. Sponsorship is not available for this position. Reasonable accommodations may be made for individuals with disabilities.

Equal opportunity statement

AAP/EEO DFWP. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

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