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MANUFACTURING TECHNICIAN II

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

TE Connectivity's Manufacturing Engineering Teams are process leaders for stamping, molding or assembly related topics, ensuring the processes are running at optimum levels for quality and output. They are experts in mold tooling, die tooling, machining, and assembly techniques, possessing extensive knowledge of the associated manufacturing processes which may include the optimization and standardization of stamping / molding / assembly or other processes within the manufacturing environment. Manufacturing Engineering Teams enable the TE business unit plants to reach TE Operating Advantage (TEOA) requirements, roll out Centers of Excellence (COE), Best Demonstrated Practices (BDP’s) and advise plants on tool and machine duplications / corrections / improvements. They design and develop manufacturing process and automation platforms and apply them for the realization of new product developments as well as optimization of existing products already in production. The Teams also support Product Development in the selection and optimization of tools for piece part production and the selection of the most suitable manufacturing concepts relative to planned manufacturing quantities, quality requirements and manufacturing location. They act as interface between engineering and production to ensure manufacturability of new designs and smooth production ramp up as well as support the research & development teams to produce sample manufacturing equipment, product samples and prototypes.

 

  • Work with R&D engineers to develop basic processes needed for catheter fabrication

  • Refine processes by carrying out DOE’s to ready processes for validations & mfg transfer

  • Oversee and run projects through pilot builds that have reached the stage of incremental improvements

  • Act as a liaison between R&D and Mfg. Engineering to carry out process training of Mfg. Engineers and assist in training operators

  • Manage / modify project documentation, assist in creating new documentation

  • Work with QE Engineers & R&D Engineers to execute and report results of validation studies

What your background should look like:

  • Associates Degree in related field preferred

  • High School diploma or equivalent is required

  • A minimum of three (3) years’ work experience in a related regulated medical device environment.

Work Location:

This position is located in Plymouth, MN

Competencies

Values: Integrity, Accountability,Teamwork, Innovation
Location: 

Plymouth, MN, US, 55441

City:  Plymouth
State:  MN
Country/Region:  US
Travel:  None
Requisition ID:  67095
Alternative Locations: 
Function:  Engineering & Technology


Nearest Major Market: Minneapolis

Job Segment: Industrial, Technician, Engineer, Maintenance, Manufacturing, Technology, Engineering

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