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TE Connectivity

Location: Brooklyn Park

Job Type: Full time


At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.

Job Overview

Responsible for quality issue documentation and resolution, analysis and trending of data, coordination and execution of training activities, receiving inspection and product release activities, auditing to regulated standards, maintenance of documentation, and executing testing with little or no supervision.


  • Document and disposition Non-Conformances, conduct & determine root cause analysis including corrective actions.
  • Conduct First Article Inspections, Inspection Method Qualifications, and Process Validation activities as required.
  • Develop/improve inspection processes, equipment/fixtures, and product flow.
  • Conduct area practice vs. procedure/Good Documentation Practice audits and follow up on findings to ensure satisfactory closure.
  • Train operators/inspectors on work instructions and procedural updates.
  • Participate in preparing & ongoing maintenance of FMEAs and Control Plans. Reporting function Quality metrics.
  • Support NPI/Operations area projects and initiatives e,g, Kaizen, yield improvement, cost reduction etc.
  • Support and/or perform batch review and release of the product.
  • Follow up on Corrective Actions for in-process and customer complaint issues.
  • Processing procedure changes.
  • Provide support for internal, customer, and external audits to ISO 13485.
  • Participate/drive quality improvement projects/activities.
  • Other tasks as directed by the functional area Quality Manager/Engineer.

What your background should look like:


  • Associate Degree in related discipline preferred (work experience may suffice in lei of degree)
  • 2 years of medical device or similar regulated industry experience
  • Excellent organization skills with strong attention to detail
  • Strong written and oral communication skills
  • Excellent skills in interpersonal relationships, communication, teamwork, and collaboration
  • Solid computer skills and proficiency in Microsoft Office
  • Work independently and possess a high level of self-motivation and initiative
  • Clear understanding of medical device quality systems and requirements.
  • Experience in product inspection techniques
  • Knowledge of root cause analytical and problem-solving skills


Values: Integrity, Accountability, Teamwork, Innovation