Operations Intern

Kimball ElectronicsIndianapolis, IN
13d

About The Position

The mission of the Operations Intern is to ensure the highest standards of product quality and compliance by mastering our assembly processes and helping in the launch of new production processes. You will drive improvements while meeting goals of quality, cost and delivery for our customers. This position is for Summer 2026. The Operations Intern will support the department by actively participating in assembly and manufacturing processes. You will have the opportunity to master our procedures and protocols while developing new ways to improve our processes. You will be leading or assisting in projects aimed at improving safety, quality and efficiency within the operations department. You will be able to collaborate with the engineering team to provide feedback on design and assembly processes in a medical device manufacturing setting. This role provides an opportunity to apply theoretical learnings to real-world experiences in a manufacturing environment with a strong emphasis on hands-on assembly experience. To be successful the candidate must be self-motivated, possess excellent communication skills, time/project management skills, a positive attitude, be able to keep timely consistent and accurate records of work. In our business, it is critical the candidate can demonstrate a solid understanding of the importance of quality.

Requirements

  • Self-motivated
  • Excellent communication skills
  • Time/project management skills
  • Positive attitude
  • Be able to keep timely consistent and accurate records of work
  • Demonstrate a solid understanding of the importance of quality

Responsibilities

  • Actively participating in assembly and manufacturing processes
  • Mastering procedures and protocols while developing new ways to improve our processes
  • Leading or assisting in projects aimed at improving safety, quality and efficiency within the operations department
  • Collaborating with the engineering team to provide feedback on design and assembly processes in a medical device manufacturing setting
  • Records complete and accurate information for Device History Records per Good Manufacturing Practices
  • Performing root cause analysis and suggesting improvements to the process
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