Manufacturing Tech II - 1st Shift M-F (6:00 AM - 2:30 PM )

GE Healthcare•West Milwaukee, WI

6d•Onsite

About The Position

The Advanced Manufacturing Technician 6 performs diverse and complex assignments in support of GE HealthCare product development and manufacturing. Assignments may include, but are not limited to: manufacturing, troubleshooting & root cause analysis, assembly, fabrication and assembly of fixtures and equipment, set up and running of data acquisition equipment for tests and assembly operations, lead compliance and quality activities and train other team members. Advance Manufacturing Technician Main responsibilities include but not limited to equipment set up, troubleshooting of equipment, understanding of quality data graphics for quality monitoring, escalation of quality and equipment deficiencies, proper documentation according to company guidelines, lite assembly for production, able to follow company operating manufacturing standards for equipment and manufacturing production, basic communication skill both verbal and written to report/document data results. Safety oriented mindset and able to meet delivery goals in a timely manner. GE HealthCare is a leading global medical technology and digital solutions innovator. Our mission is to improve lives in the moments that matter. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.

Requirements

Associates Degree with a minimum of 3 years manufacturing experience or High School diploma/GED with a minimum of 5 years manufacturing experience
Utilize basic technical communications throughout the new product cycle to improve internal models and/or externally sourced components in terms of system performance, reliability, functionality, and serviceability
Perform basic trouble shooting encompassing multiple variables and unknowns to achieve root cause analysis and problem resolution.
Conduct experiments and diagnostic tests, as required to draw conclusions
Test production assemblies and sub-assemblies for correct operation and compliance to performance specifications
Familiarity with quality monitoring tools and interpreting quality data graphics
Prior experience in medical device or other regulated manufacturing environments
With limited guidance, carry out experiments in which the approach and methods have been outlined.
Perform a variety of measurements, obtain and prepare data, make competent experimental observations and report the results
Recognize equipment irregularities, which would indicate new or unexpected phenomena or would tend to disrupt the manufacturing process. Bring irregularities to the attention of the supervisor
Intermediate computer skills, including data entry and navigating manufacturing systems
Provide evaluation, constructive feedback and leadership
Ability to read, write, and communicate in English, including documentation and reporting

Responsibilities

Utilize basic technical communications throughout the new product cycle to improve internal models and/or externally sourced components in terms of system performance, reliability, functionality, and serviceability
Perform basic trouble shooting encompassing multiple variables and unknowns to achieve root cause analysis and problem resolution.
Set up and operate manufacturing equipment according to standard operating procedures
Monitor quality data and interpret graphical trends to ensure product compliance
Document production and quality data accurately and in accordance with company guidelines
Follow all safety protocols and contribute to a culture of continuous improvement
Conduct experiments and diagnostic tests, as required to draw conclusions
Make acquired skills or knowledge available to others train others on manufacturing processes
Test production assemblies and sub-assemblies for correct operation and compliance to performance specifications
With limited guidance, carry out experiments in which the approach and methods have been outlined.
Perform a variety of measurements, obtain and prepare data, make competent experimental observations and report the results
Recognize equipment irregularities, which would indicate new or unexpected phenomena or would tend to disrupt the manufacturing process. Bring irregularities to the attention of the supervisor
Provide evaluation, constructive feedback and leadership in the development of internal and external engineering, manufacturing, or service documentation
Maintain complete and accurate records of all work. As required, with guidance, provide data for formal reports (oral and written) of the work. Also prepare and submit, with guidance, appropriate disclosure letters of patentable ideas when a contribution has been made and evaluated by the supervisor
Collaborates with other departments in the planning & execution of duties to ensure the orderly flow of material and information
Maintains daily production output
Works with team lead, engineers, supervisors, and managers to improve quality and process efficiency
Complies with all EHS and Quality procedures and policies