Crimp Technician (First Shift - Onsite)

Insulet Corporation•Irvine, CA

3d•Onsite

About The Position

The Crimping Department position works with small, detailed projects and products, production assembly, and detail-oriented machines that make small parts. It also assists with minor and miscellaneous tasks as requested. The role performs equipment setup, operation, minor repairs, and basic daily preventative maintenance under minimal supervision while meeting safety, quality, and efficiency standards. It is an onsite position in a medical-device manufacturing environment.

Requirements

High school diploma preferred.
Ability to use basic hand tools.
Basic computational skills.
Proficiency in English to read documentation, communicate, and write.

Nice To Haves

Associate degree.
Some manufacturing experience.
Familiarity with manufacturing instruments such as micrometers, calipers, feeler gauges, dial indicators, and gauge blocks.
Ability to handle a variety of tasks in a fast-paced, multitasking environment.
Keen eye for quality, dependability, collaborative teamwork, and a positive attitude.
Mechanical aptitude and some experience with automated machines and tools, including their design, uses, repair, and maintenance.
Some Excel experience.

Responsibilities

Set up, operate, make minor repairs to, and perform basic daily preventative maintenance on equipment under minimal supervision.
Maintain machine raw-material feeds and clear faults and stoppages on automated equipment.
Use human-machine interfaces (HMIs) to identify and correct shifts in process control.
Prepare adequate raw materials correctly and run jobs in a timely manner to support on-time delivery.
Troubleshoot mechanical errors or safety issues and identify potential solutions using a troubleshooting table.
Use computer systems to support material inventory and quality-management processes.
Participate in new-product design transfer, process development, equipment validations, and process validations.
Use measuring tools to ensure correct tolerances.
Operate machines or test parts efficiently with minor supervision.
Assist the IQA department.
Work from specifications, work orders, and general instructions from Production Leads.
Follow standard operating procedures and Good Manufacturing Practices (GMPs), including procedures for material handling, record keeping, packaging, and shipment preparation.
Notify the Team Leader or Production Supervisor of discrepancies and maintain quality standards and operational safety.
Work in small groups and cross-functional teams to troubleshoot issues and identify and implement corrective actions.
Maintain a clean work environment suitable for medical-device manufacturing.
Perform other duties as required.