HC_Production Associate 1

GE HealthCare•Noblesville, IN

2d•Onsite

About The Position

GE HealthCare in Noblesville is seeking experienced manufacturing and repair technicians to support the manufacture, configuration, refurbishment, and repair of ultrasound machines. The role evaluates and repairs equipment and components, completes system upgrades, verifies equipment operation, documents test results, and maintains accurate inventory and equipment records. The position also supports product quality, safety, process efficiency, on-time delivery, and customer outcomes while working with engineers, team members, and site leaders. The position requires compliance with the Quality Management System, applicable laws and regulations, controlled documentation, training requirements, and site safety policies. Candidates must have a high school diploma or local equivalent, at least two years of relevant experience, English communication skills, and demonstrated capabilities in at least three of the listed key skills. GE HealthCare will not sponsor employment visas for this opening. Employment is conditional on successfully completing a drug screen, as applicable.

Requirements

High school diploma or local equivalent.
Two or more years of relevant experience.
Ability to communicate, receive, and understand written and verbal instructions in English.
Ability to work independently and as part of a team, with varied daily tasks and responsibilities.
Excellent attendance, accountability, teamwork, personal initiative, and work ethic.
Excellent time management skills, desire to learn, and a flexible approach to daily work tasks.
Demonstrated attention to detail and focus on product quality and safe working practices.
Demonstrated capabilities in at least three of the listed key skills: mechanical aptitude, troubleshooting, technical documentation, computer proficiency, and process improvement.

Nice To Haves

Associate degree or higher in a technology- or engineering-related discipline.
Previous experience in a manufacturing or service role in a regulated industry, such as medical devices.
Demonstrated capabilities in all listed key skills: mechanical aptitude, troubleshooting, technical documentation, computer proficiency, and process improvement.

Responsibilities

Comply with Quality Management System requirements and applicable laws and regulations.
Use controlled, released documentation to perform work tasks and processes.
Maintain required training records and comply with site safety policies.
Evaluate and identify damaged components, order replacement parts, and create work orders.
Disassemble systems, clean components, and repair or replace damaged parts.
Complete required service corrective actions and system software or hardware upgrades.
Reassemble systems and install required options and accessories.
Verify system operation through diagnostic and functional tests.
Record test results and update Device History Records for each piece of equipment.
Identify, segregate, and disposition or redirect products that fail acceptance criteria.
Maintain accurate inventory records, including the status and location of parts and systems.
Properly maintain tools and test equipment and ensure calibrations are complete.
Identify manufacturing issues and assist with corrections to drive product quality.
Work with engineers, team members, and site leaders to improve process quality and efficiency.
Help improve on-time delivery and overall customer outcomes and experience.