Equipment & Automation Engineer II - Manufacturing Support

Thornton Tomasetti

Madison (WI)

On-site

USD 61,000 - 123,000

Full time

2 days ago
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Job summary

Abbott Cancer Diagnostics in Madison, WI seeks an Equipment and Automation Engineer II to provide manufacturing support for existing equipment and to help launch new equipment into Production. You will work cross-functionally, triage issues, drive improvements, and ensure machines are properly supported throughout their life cycle in a regulated environment.

Responsibilities include developing build procedures, documenting changes, supporting testing of custom equipment, and adhering to FDA,

Qualifications

  • Bachelor's degree in Engineering; 2+ years of experience, or an Associate degree with 4+ years of experience.
  • Knowledge of engineering theories, practices and procedures and applies this to assignments.
  • Demonstrated ability to drive projects to successful completion.

Responsibilities

  • Develop process and procedures for building new equipment.
  • Apply defined procedures to execute and document changes to existing equipment.
  • Create, document, and execute protocols to support process or part changes.
  • Investigate problems, gather facts, analyze data, and draw accurate conclusions.
  • Troubleshoot and repair equipment.
  • Support failure analysis investigations and root cause analysis with support from more experienced team members.

Skills

Project management
Analytical thinking
Cross-functional collaboration
Documentation

Education

Bachelor's degree in Engineering
Associate degree in Engineering/Technology/Electronics

Tools

Electronic Quality Management Systems
Manufacturing Software Systems

Job description

Abbott Cancer Diagnostics in Madison, WI seeks an Equipment and Automation Engineer II to provide manufacturing support for existing equipment and to help launch new equipment into Production. You will work cross-functionally, triage issues, drive improvements, and ensure machines are properly supported throughout their life cycle in a regulated environment.

Responsibilities include developing build procedures, documenting changes, supporting testing of custom equipment, and adhering to FDA,

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