Wire Technician (Weekday Shift - Onsite)

Insulet Corporation•Acton, MA

12d•$18 - $27•Onsite

About The Position

The Wire Technician operates detail-sensitive machines making small parts and works with their hands on small, detailed projects. This is a weekday shift with working hours from 6:00 am - 6:30 pm, Monday - Thursday. The position is working on-site at our Acton, MA location and requires on-site office/plant/lab work.

Requirements

Self-starter capable of dealing with a variety of tasks in a fast paced, multi-tasking environment.
Must be proficient in English language to be able to read documentation, communicate, and write.
Ideal candidate will have keen eye for quality, is dependable, and will work collaboratively within a team, and possess a positive attitude.
Mechanical Aptitude – Knowledge of and experience with automated machines and tools, including design, uses, repair, and maintenance.
Production & Processing – Knowledge of raw materials, measurement instruments, production processes, quality control, and other techniques for the manufacture and distribution of goods.
Mathematics – Knowledge of basic arithmetic, algebra and/or geometry.

Nice To Haves

High School Diploma/GED
Experience in manufacturing
Experience with assembling, debugging, and optimizing discrete component assembly processes

Responsibilities

Perform equipment setup, operation, repair, and basic daily/weekly preventative maintenance tasks to meet all standards for safety, quality, and efficiency.
Maintain machine raw material feeds, perform any fault clearing and clear stoppages on automated equipment.
Utilize human machine interfaces (HMIs) to identify and correct shifts in process control.
Ensure adequate raw material is prepared correctly and jobs are on schedule.
Able to utilize computer systems to support material inventory and quality management processes.
Perform routine cleaning/inspection/lubrication of machinery.
Able to use measuring tools to assess process stability and product quality.
Works from specifications, work orders, and general instructions from Supervisor.
Safely follow standard operating procedures including but not limited to material handling, record keeping, packaging, and shipment preparation.
Identify and report discrepancies in quality, safety and process execution.
Ensure adherence to SOPs and regulatory standards (FDA 21CFR, ISO 13495, cGMP).
Able to work in small groups and cross functional teams to troubleshoot issues, identify and implement collective corrective actions.
Maintain a clean work environment suitable for medical device manufacturing.
Performs other duties as required.