Crimp Technician (First Shift - Onsite)

Insulet Corporation•Irvine, CA

12d•Onsite

About The Position

The Crimp Technician position involves assembling small, detailed components in a fast-paced production environment. The role requires operating and maintaining automated equipment, monitoring processes, troubleshooting minor issues, and ensuring products meet strict quality and safety standards. This position demands attention to detail, basic mechanical aptitude, and the ability to work both independently and as part of a team. Ideal candidates are dependable, comfortable using tools and measuring instruments, and thrive in a clean, regulated (medical device) setting.

Requirements

H.S. diploma preferred.
Ability to use basic hand tools.
Basic computational skills.
Proficient in English language to be able to read documentation, communicate, and write.
Mechanical Aptitude and some experience with automated machines and tools, including design, uses, repair, and maintenance.

Nice To Haves

Associate degree is a plus.
Some manufacturing experience is a plus.
Familiarity with manufacturing instrumentation such as micrometers, calipers, feeler gauges, dial indicators, and gauge blocks.
Self-starter capable of dealing with a variety of tasks in a fast paced, multi-tasking environment.
Keen eye for quality, is dependable, and will work collaboratively within a team, and possess a positive attitude.
Some Excel experience.

Responsibilities

Perform equipment setup, operation, minor repair, and basic daily preventative maintenance tasks to meet all standards for safety, quality, and efficiency.
Maintain machine raw material feeds, perform 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 run in a timely manner to ensure on-time delivery.
Troubleshoot and identify potential solutions using a troubleshooting table for mechanical errors or safety issues.
Utilize computer systems to support material inventory and quality management processes.
Participate in manufacturing processes to support new product design transfer, process development, equipment validations, and process validations.
Use measuring tools to ensure correct tolerances.
Operate machines or test parts with minor supervision, efficiently.
Assist the IQA department.
Work from specifications, work orders, and general instructions from Production Leads.
Safely follow standard operating procedures including but not limited to material handling, record keeping, packaging, and shipment preparation.
Follow all Good Manufacturing Practices (GMPs).
Notify Team Leader or Production Supervisor of any discrepancies.
Ensure quality standards and safety of operations are maintained at all times.
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.
Perform other duties as required.