Crimp Technician (Third Shift - Onsite)

Insulet Corporation • Irvine, CA

1d • Onsite

About The Position

We’re seeking a reliable and detail-oriented Crimping / Manufacturing Associate to join a collaborative production team. In this role, you’ll work with specialized equipment and small, precision components—playing a key part in producing high-quality products in a fast-paced, regulated environment. The Crimping Department position works with their hands on small, detailed projects and products, production assembly, detail-oriented machines making small parts and assists with minor/miscellaneous tasks as requested.

Requirements

• 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

• H.S. diploma preferred.
• 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.
• Ideal candidate will have 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 any fault clearing and clear stoppages on automated equipment.
• Utilize human machine interfaces (HMIs) to identify and correct shifts in process control.
• Ensures 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.
• Utilizes computer systems to support material inventory and quality management processes.
• Participates in manufacturing processes to support new product design transfer, process development, equipment validations, and process validations.
• Uses measuring tools to ensure correct tolerances.
• Operates machines or tests the parts, with minor supervision, efficiently.
• Assists the IQA department.
• Works 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.
• Must follow all Good Manufacturing Practices (GMPs).
• Notifies Team Leader or Production Supervisor of any discrepancies.
• Ensures quality standards and safety of operations are maintained at all times.
• 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.

Benefits

• Consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
• Healthy work and life balance.
• Support to help employees get there.
• Culture that supports curiosity, innovation, and learning.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: High school or GED