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Requisition ID:  2156
Location:  Plymouth, MN, US, 55446
Alternative Locations: 
Education Experience:  -
Employment Experience:  -
Travel:  None

Company Information

TE Connectivity (NYSE: TEL) is a $12 billion global technology leader. Our connectivity and sensor solutions are essential in today's increasingly connected world. We collaborate with engineers to transform their concepts into creations - redefining what's possible using intelligent, efficient and high-performing TE products and solutions proven in harsh environments. Our 72,000 people, including over 7,000 engineers, partner with customers in over 150 countries across a wide range of industries. We believe EVERY CONNECTION COUNTS -

The TE Medical business unit, part of the Industrial Solutions segment, offers medical device OEMs, a complete product offering, and capability portfolio for minimally invasive, imaging, surgical, diagnostic, and therapeutic devices. With more than 350 design engineers and a global presence in all key medical device hubs, we are a premier partner to the world's leading medical technology companies for their next-generation medical devices. We are experts in all aspects of device design and manufacture, from access and delivery solutions for interventional medicine; to sensors and connectors for surgical applications. Our innovative solutions enable ground breaking medical therapies such as treating heart disease without opening the body, placing microscopic devices into brain arteries and powering robotic surgery.

Job Overview

Job Overview

TE Connectivity's Manufacturing/Production Teams transform raw materials into finished goods and ensure component flow. They perform changeovers and setups according to production schedule, perform quality checks according to established processes and document the results as required by our quality procedures. Every team member is responsible for maintaining housekeeping and organization of the work area as well as following TE Connectivity's EH&S policies and procedures.

This position is scheduled to work 2nd shift or Split-Shift (2nd overlapping 3rd).

Responsibilities & Qualifications

This role is responsible for performing a wide variety of operations in support of production, quality and safety goals.
•Confer with management or subordinates to resolve worker problems, complaints, or grievances.
•Conduct performance reviews and set expectations and goals and objectives for employees.
•Enforce safety and sanitation regulations.
•Direct and coordinate the activities of employees engaged in the production or processing of goods.
•Confer with other supervisors and managers to coordinate operations and activities within or between departments.
•Demonstrate equipment operations and work and safety procedures to new employees, or assign employees to experienced workers for training.
•Ability to perform and demonstrate all Manufacturing procedures after training.
•Ability to train operators on manufacturing procedure.
•Read and analyze charts, work orders, production schedules, and other records and reports to determine production requirements and to evaluate current production estimates and outputs.
•Accurately completes all essential documents (i.e., Lab Notebooks, Device Master Records (DMR’s), Lot History Records (LHR’s), Inspections records and validation documentation).
•Monitor the sign-off of routing paperwork and verify the in-process testing is done on time and accurately.

EDUCATION and/or EXPERIENCE: High School Diploma and/or GED or equivalent experience, post secondary education preferred. Minimum of 3 years experience as a production supervisor or lead in a manufacturing environment; preferably medical device.


  • Values: Integrity, Accountability,Teamwork, Innovation
  • SET : Strategy, Execution, Talent (for managers)


Nearest Major Market: Minneapolis

Job Segment: Industrial, Manager, Manufacturing, Management

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