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Kimball Electronics · 3 months ago

Injection Molding Technician, 2nd Shift

Kimball Electronics Indianapolis

Full-time

Onsite

Entry Level

2+ years exp

Kimball Electronics is a company committed to providing quality medical solutions, and they are seeking an Injection Molding Technician to run production molded parts and assist with maintenance and engineering projects. The role requires attention to detail and accuracy while meeting quality, cost, and delivery goals for customers.

ElectronicsManufacturing

No H1B

Responsibilities

Run production injection molded parts per production procedures

Assist with molding maintenance requirements and engineering projects

Document molding activities while meeting goals of quality, cost and delivery for customers

Perform basic maintenance of the plastic injection molds and equipment

Assist engineering with special projects as required

Help develop molding processes and written procedures

Train operators and perform other production tasks

Qualification

Injection molding machineryTroubleshooting injection moldingMold set-upProcessingISO-13485 knowledgeDocumentation practicesMechanical inclinationVisual inspection skillsLift 55 lbsClimb ladderTeam collaborationAdaptability

Required

Mechanically inclined person with 2 years relevant work experience with knowledge of setting tools for production and processing tools

Experience using injection molding machinery including testing devices, meters, moisture analyzers, chiller, thermometers, raw material handling system, mold heat controllers, and mold presses

Experience troubleshooting issues with injection molding equipment and processes

Ability to monitor production on multiple injection molding machines at the same time

Good documentation skills

Ability to lift up to 55 lbs

Ability to climb a ladder

Visual parts inspection including 20/20 vision (corrected)

React to change productively and handle other tasks that may be assigned

Understand business, legal and regulatory requirements

Work overtime when needed

Maintain general knowledge of the certification and regulatory requirements contained in ISO-13485, and FDA CFR/GMP Medical Device Regulation