HC_Production Associate 1

GE HealthCare•Noblesville, IN

4d•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 involves working with controlled documentation and quality management requirements to inspect, service, test, and document equipment. The associate also maintains inventory and equipment records, supports product quality and process improvements, and works with engineers, team members, and site leaders to improve efficiency and customer outcomes. The position requires a high school diploma or local equivalent and at least two years of relevant experience. Applicants must demonstrate capabilities in at least three of the listed key skill areas. An associate degree or higher in a technology- or engineering-related discipline and experience in manufacturing or service work in a regulated industry are preferred. GE HealthCare does not sponsor employment visas for this opening. Applicants must be legally authorized to work in the United States. Employment offers are conditioned on successfully completing a drug screen, as applicable. Some customer vaccination mandates may apply to certain employees.

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 flexibility in daily work tasks.
Attention to detail and focus on product quality and safe working practices.
Demonstrated capabilities in at least three key skill areas: mechanical aptitude, troubleshooting skills, 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 skill areas.

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.