דרושים ב-Ge Healthcare ב-United States, Salt Lake City

Performs diverse assignments in support of GEHC service operations. Assignments may include but are not limited to:System Level Harvesting
Sub-Assembly Build and Test
Reporting/documenting results of tests and measures
Receiving and Evaluation of components
Essential Responsibilities:

• Interfaces with other departments in the execution of duties to ensure the orderly flow of material and information

• Execute training plans

• Perform basic trouble shooting encompassing multiple variables and unknowns to achieve root cause analysis and problem resolution

• Utilize basic technical communications throughout the test process for production/Refurb assemblies/systems

• Provide evaluation/constructive feedback in the development of internal and external engineering, manufacturing, or service documentation

• Provide strong individual contributions to team goals

• Participate in LEAN process improvement activities to improve quality, process flow, and cycle or TAKT times

• Comply with EHS regulations and policies and escalate concerns/suggestions to leadership

• Maintain daily production output

• Identify and report defects in assigned area

• Engage in daily 5s activities

Qualifications/Requirements:

• High School diploma/GED or Local Equivalent and 2 years technical experience

• Ability to work independently

• Demonstrated basic computer skills and ability to navigate online instructions

• Ability to draw accurate conclusions from test data, malfunctions, or deviations, and assist with corrections to the existing design or process

Desired Characteristics:

• Associates degree in an Electronics or Engineering field

• Electrical experience

• Experience in medical manufacturing or other highly regulated industry preferred.

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.

Roles and Responsibilities

• Lead the Advanced Science and Image Quality Engineering function for the Surgery business
• Establish and sustain criteria for the execution of image chain development on New Product Introductions (NPIs)
• Promote a culture of innovation and collaboration to build the imaging roadmap
• Provide technology differentiation, functional excellence and teamwork
• Attend customer visits and clinical training sessions
• Establish and maintain relationships with external partners to allow for collaboration on imaging algorithms
• Champion a culture that ensures outstanding compliance and adherence to product quality in all areas for the Quality Management System in GEHC
• Ensure that the organizational design, functional expertise, engineering process experience of the technology team is positioned to exceed customer expectations
• Formulate the strategy for continuous improvement of systems, products and processes
• Engage in cross-functional activities, including recruitment, retention, talent acquisition, team development, and mentoring
• Inspire team’s engagement in all phases of product development
• Support existing products within Manufacturing, Sourcing, Service and Supplier Quality Engineering

Required Qualifications

• Bachelor’s Degree in Computer Science or in STEM Majors (Science, Technology, Engineering, Math)
• Minimum of 5 years of professional experience in project or people leadership within a product development or research development environment
• 3 years project management or direct / indirect people leadership experience

Desired Characteristics

• Masters or PhD in Engineering or Physics
• 7 years relevant industrial experience
• Proven ability to work cross-functionally

We will not sponsor individuals for employment visas, now or in the future, for this job opening.

• Set up and running of data acquisition equipment for tests
• Reporting/documenting results of tests and measures
Essential Responsibilities

• Test production/Refurb assemblies/systems for correct operation and compliance to performance specifications.

• Ability to demonstrate proficiency using a Digital Multimeter, Oscilloscope, and Power Supplies.

• Perform electrical calibration on production/refurb systems and subassemblies.

• Interfaces with other departments in the execution of duties to ensure the orderly flow of material and information.

• Execute training plans.

• Perform basic trouble shooting encompassing multiple variables and unknowns to achieve root cause analysis and problem resolution. Conduct diagnostic tests, as required to draw conclusions.

• Interpret circuit board schematics/system interconnect diagrams.

• Utilize basic technical communications throughout the test process for production/Refurb assemblies/systems.

• Provide evaluation/constructive feedback in the development of internal and external engineering, manufacturing, or service documentation.

• Provide strong individual contributions to team goals.

• Participate in LEAN process improvement activities to improve quality, process flow, and cycle or TAKT times.

• Comply with EHS regulations and policies and escalate concerns/suggestions to leadership.

• Maintain daily production output.

• Identify and report defects in assigned area.

• Engage in daily 5s activities.

Required Qualifications

• Associates degree in an Electronics or Engineering field, or a technical certificate from a qualifying school with at least 25 credit hours in electronics including classes in electronics assembly, DC/AC/analog electronics, digital fundamentals, troubleshooting, and instrumentation, or a High School diploma and 2 years Electronics experience.

• Proficiency to logically troubleshoot at subsystem and system level, using identifiable problem-solving techniques

• Ability to draw accurate conclusions from test data, malfunctions, or deviations, and assist with corrections to the existing design or process

• Must be able to physically lift (floor to waist, waist to crown level, and horizontally)

• Lift and carry up to 35 lbs. (Anything over 35 lbs. requires assistance.)

• Must be able to perform frequent simple grasping, firm grasping, fine manipulation, neck rotation, and neck flexion frequently throughout the workday

• Must be able to twist, push/pull, reach at, above and below shoulder height frequently throughout the workday

• Must be able to frequently stoop, bend, squat and kneel throughout the workday

• Must be able to stand/sit continuously throughout the day

• Must be able to ascend/descend/balance occasionally on portable step stools

Desired Characteristics

• Bachelor’s degree in manufacturing, Engineering or Technology related fields.

• Experience in medical manufacturing or other highly regulated industry preferred.

Executes the receiving, storing, staging and distribution of materials required for assembly/manufacturing of product.
Job Description

While GE HealthCare does not currently require U.S. employees to be vaccinated against COVID-19, some GE HealthCare customers have vaccination mandates that may apply to certain GE HealthCare employees.

The Image Quality Engineer is responsible for research and development for new and existing imaging products in the GE HealthCare Surgery product line. They prove a concept to be valid by the application of scientific and engineering methodologies. Their work typically has the objective of demonstrating through test or analysis the performance and implementation potential of a concept. Requires mastery of a body of theoretical knowledge. Requires developed and strong foundation of function skills and knowledge of relevant technologies.

Essential Responsibilities

Duties include (but are not limited to):

• Specifying requirements which can be implemented by the engineering team
• Executing design to engineering standards
• Developing methods to quantify subsystem interactions and their effects on image quality
• Verification and validation of system features and sub-systems relating to X-ray exposure control, image processing, and visualization.
• Working within a team to deliver technical solutions
• Working with external collaborators and/or technical leadership to ensure that the technical deliverables are consistent with the goals of larger programs, projects or initiatives

BS in Life Sciences, Chemistry, Physics, Biomedical Engineering, Electrical Engineering, or related field and 4 years relevant work experience.

This role is for 3rd shift, 11:00 PM - 7:30 AM EST.

Responsibilities

• Performs manufacturing and maintenance work from detailed work instructions and operational method sheets.

• Maintains daily production output with accurate records of the work performed and other records as may be required by management.

• Make limited decisions within the confines of quality and safety approved procedures, with guidance.

• Mainly performing production work and may be dependent upon others for non-standard work. Flexibility and adaptability expected.

• Complies with all EHS, Training and Quality procedures and policies

• Perform routine troubleshooting of process or equipment. Brings equipment irregularities to the attention of the supervisor.

• Use Lean tools to improve established processes and metrics in daily work. Participates in Action Workouts and Kaizen events.

• Make acquired skills or knowledge available to others; train others on manufacturing processes.

• Willing to cross-training in other areas of manufacturing process to assist in site goals.

• All other duties as assigned.

Required Qualifications

• Associates degree in Applied Sciences (or local equivalent 2 year degree)ORa High School diploma (or local equivalent)and2 years technical experience in relevant industry.

• Proficiency to understand and interpret basic written technical information.

• Demonstrated ability to work well with general direction and information.

• Demonstrated proficiency to utilize computerized work

• Effective verbal and written communication skills with teammates, management, and across functions.

• Being able to sit and/or stand for long periods of time.

• Ability to work in a clean room environment including wearing the required PPE for long periods of time.

Preferred Qualifications

• Knowledge of semiconductor manufacturing process and/or thin film deposition.

• Experience with vacuum systems, compressed gases, RF power, PLC & computer systems strongly preferred

• Demonstrated experience working in quality-controlled environment, specifically FDA-regulated medical product manufacturing or another relevant environment.

• Demonstrated strong problem-solving / equipment troubleshooting skills.

• Mechanical, facilities and/or maintenance experience.

• Experience working in a cleanroom environment.

• Lean / Six Sigma experience.

We will not sponsor individuals for employment visas, now or in the future, for this job opening.

Responsibilities

• Provide clear direction and leadership to a team of skilled Technicians

• Conduct employee performance reviews, set individual and team goals, and deliver ongoing coaching to enhance development, engagement, and performance.

• Ensure timely material procurement and accurate production forecasting based on deliverable needs; monitor time-sensitive materials closely

• Monitor and improve productivity while ensuring customer commitments are met with high quality, timeliness, and cost efficiency.

• Plan and execute production tasks to optimize tool utilization and labor efficiency, maximizing throughput

• Lead and support documentation activities related to medical device manufacturing, ensuring compliance with regulatory requirements

• Develop and implement training plans to build workforce capability and flexibility

• Lead compliance and Environmental, Health & Safety (EHS) initiatives in alignment with plant goals

• Drive implementation of LEAN manufacturing practices to improve operational efficiency

• Communicate with material and tool vendors as needed to coordinate maintenance and servicing in collaboration with the engineering team

• Coordinate process flow for Device History Records (DHRs), manage data within electronic record systems, and oversee tool maintenance schedules

• Manage P&PC change control procedures in partnership with engineering for changes impacting process qualification or production toolsets

• Execute business unit objectives and manufacturing department goals across all functional areas

• Perform other duties as assigned

Quality Specific Goals:

• Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position

• Complete all planned Quality & Compliance training within the defined deadlines

• Identify and report any quality or compliance concerns and take immediate corrective action as required

• Maintaining full Quality System Regulation and Current Good Manufacturing Practices requirements

• Maintaining full regulatory compliance and other legal requirements

• Knowledge and understanding of production process Work Instructions and operates within them to ensure that a device conforms to its specifications

• Ensures the creation of accurate, complete, and timely records and DHRs

Required Qualifications

• Bachelor’s Degree in an engineering or technical discipline and 2 years semi-conductor manufacturing, supply chain, or leadership experience, or Associate’s Degree in an engineering or technical discipline and 4 years semi-conductor, supply chain experience, or leadership experience, or HS Diploma/GED with 6 years semi-conductor manufacturing, supply chain, or leadership experience

• Demonstrated ability to lead and develop teams.

• Strong mechanical aptitude and experience running critical manufacturing tool sets

• Demonstrated ability to implement and qualify processes and procedures within a regulated industry

• Excellent oral and written communications skills to employees at all levels of an organization

• Demonstrated ability to identify and implement best practices and deal with high levels of ambiguity

• Demonstrated ability to operate independently and exercise good discretion, troubleshooting, and decision-making

Desired Characteristics

• Prior team leading or supervisory experience

• High proficiency to interpret, instruct, and explain complex technical information

• Fast learner with ability to synthesize data and draw conclusions accordingly

• Familiarity and experience with Quality Management Systems in an FDA regulated environment

• Six Sigma certified

We will not sponsor individuals for employment visas, now or in the future, for this job opening.