Production Maintenance Technician M- F 7am - Pm jobs at Ge Healthcare in United States, City Of Troy
GE HealthCare Service Engineering Technician United States, Utah, Salt Lake City
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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
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
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.
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GE HealthCare Electronics Technician 1st Shift - M-F – PM United States, Utah, Salt Lake City
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• 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.
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.
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GE HealthCare Manufacturing Technician M- F PM - United States, New York, City of Troy
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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.
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.
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.
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GE HealthCare Production Team Leader United States, New York, City of Troy
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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
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
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
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GE HealthCare Production Maintenance Technician M- F 7AM - PM United States, New York, City of Troy
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Responsibilities
Responsible for the daily preventative maintenance, troubleshooting, repair, and optimization of manufacturing equipment. Processing equipment includes Wet etching, Dry etching, and Photolithography, PVD, PECVD, and Chemical plating processes.
Perform support for tracking/trending of the systems for control and increased system uptime.
Troubleshooting electronics on process equipment.
Perform trouble shooting, program reloading, and minor PLC or HMI programing for various type controllers and interfaces.
Perform repair and maintenance on system robotics.
Process knowledge of high vacuum processing equipment, to be able to troubleshoot, repairs, and optimize uptime.
Maintain complete and accurate records of all work and provide data for formal reports (oral and written) as required.
Develop SOPs, work instructions, and execute training plans as required.
Use judgment to determine proper troubleshooting steps or improvement to processes.
Collaborate with other departments in the planning & execution of duties to ensure the orderly flow of material and information.
Adjust variables as directed, take specified data, and bring equipment irregularities to the attention of the supervisor. Make a variety of specified measurements and manipulations with skill.
From detailed instructions, set up or modify equipment, calibrate and operate equipment.
May participate in quality control inspections.
Work with Facilities Manager, engineers, supervisors, and other managers to improve quality and process efficiency.
Understand and execute LO/TO principles.
Comply with all EHS and Quality procedures and policies.
Associate Degree in Applied Science field plus 3 years or more of related experience; or any Associate Degree plus 4 years or more of related experience; or a Bachelor of Science degree in Applied Sciences field; OR High School Diploma/GED plus 5 years or more of related experience OR equivalent overall related experience and/or education in lieu of specific degrees.
Demonstrated project management & project execution skills.
Demonstrated ability to easily shift from one activity to another.
Demonstrated motivation to meet manufacturing outputs and continuously improve processes.
Demonstrated ability to work well with limited direction and information.
Proficiency to understand and interpret basic written technical information.
Demonstrated proficiency to utilize computerized work systems.
Effective verbal and written communication skills. Ability to communicate using English.
Legal authorization to work in the U.S. is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening
Bachelor’s degree in Engineering or closely related field Familiarity and experience with Environmental Health and Safety regulations and procedures.
Demonstrated knowledge of electronics, PLCs, HMIs, and Robotics. Demonstrate knowledge of flat panel manufacturing or semi-conductor processing equipment.
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GE HealthCare Production Associate Group Leader United States, Utah, Salt Lake City
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Essential Responsibilities:
- Responsible for ensuring team is on schedule. Adjusts people and resources as necessary to meet business objectives. Reads work procedures, work instructions, drawings (where applicable), and provides instruction to others when required.
- Audit that required tools are available and in good working order, within calibration date, and escalate if additional action is required.
- Monitor the daily production flow and adjust workloads and resources appropriately.
- Identify, report, escalate, investigate, and resolve defects.
- Assist in implementation of process improvements to increase quality and productivity levels.
- Monitor team compliance to quality assurance and environmental health and safety procedures and policies as required, and correct as needed.
- Ensure team is using current documents released in MyWorkshop used during the production process.
- Qualified and effective competency trainer of the entire work area. Check and review final product paperwork or DHR entries as needed.
- Perform other duties as assigned and may be asked to be included in quality activities, training sessions, and employee activity teams.
- Participate in quality control inspections when required.
- Fill in for the supervisor when they are out of office.
- Monitor 5S in the area and drive continuous improvement initiatives.
- Serve as the subject matter expert for the area for technical support.
- Be the first responder to eAndons and escalate until they are resolved.
- Order tools and supplies as needed to support area needs.
- Handle initial personnel issues and escalate if needed.
- Serve as a backup to fill unexpected absences.
- Update visual management boards daily.
- Follow group lead standard work.
Qualifications/Requirements:
- High School Diploma or local equivalent.
- 5 or more years of related manufacturing experience.
- Ability to communicate, receive and understand instructions regarding duties to be performed
- Ability to provide instructions regarding policies and procedures Must be able to lift (floor to waist, waist to crown level, and horizontally).
- Lift and carry up to 50 lbs.
- Must be able to perform frequent simple grasping, firm grasping, fine manipulation, neck rotation, and neck flexion 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 and bend; occasionally 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 stool.
Desired Characteristics:
- Associates degree or local equivalent.
- Prior management experience.
- Prior experience working in a medical device manufacturing environment.
- Previous experience in GMP work environment.
Other: 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.
- Training: Aware of and comply with GEHC training requirements.
- Knowledge and understanding of production process, work instructions, documentation configuration control, non-conforming & rework documentation requirements and operates within them to ensure that a device conforms to its specification.
- Aware of and comply with Stop Order, Concessions, ESD, Calibration, Preventative Maintenance, Material Identification & Segregation, and Good Documentation Practices, as associated with this job type/position.
Additional Eligibility Qualifications:
GE will only employ those who are legally authorized to work in the United States for this opening. For this role sponsorship is not provided. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).
We will not sponsor individuals for employment visas, now or in the future, for this job opening.These jobs might be a good fit
GE HealthCare Production Associate United States, Utah, Salt Lake City
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The production associate may have responsibilities including manufacturing, assembly, cleaning, packaging, and shipping of products. This is a team line environment where one operator passes their work to the next operator in queue.
Essential Responsibilities:
- Performs entry to mid-level manufacturing/assembly operations on production line and other various tasks following procedures, work instructions, and process aid sheets
- Uses lift platforms, hoist, torque tools, and other power hand tools to assemble machines
- Reads and follows work procedures or receives verbal instructions regarding duties to be performed
- Demonstrates excellent verbal and written communication skills
- Maintains daily production output
- Cross trains and work in multiple functions for business flexibility
- Follows all EHS and Quality policies and procedures
- May participate in quality control inspections
- Works with team lead, engineers, supervisors, and managers to improve quality and process efficiency
- Other duties as assigned, and may be asked to be included in quality activities, training sessions, and employee activity teams
- Complies with EHS regulations and policies
- Complies with attendance policies and be willing to work voluntary overtime when needed.
Qualifications/Requirements:
- High School Diploma/GED or local equivalent or 6 months of manufacturing experience
- Ability to communicate, receive and understand instructions regarding duties
to be performed - Demonstrated ability to detail and quality-minded work habits
- Demonstrated ability to communicate with co-workers and leadership
- Must be willing to submit to a background investigation, including for example, verification of past employment, criminal history, and educational background
- Must be willing to take a drug test
- Must be legally authorized to work in the United States
- Must be willing to work out of an office located in Salt Lake City, Utah
- Must be able to lift (floor to waist, waist to crown level, and horizontally)
- Lift and carry up to 50 lbs.
- Must be able to perform frequent simple grasping, firm grasping, fine manipulation, neck rotation, and neck flexion 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 and bend; occasionally 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 stool
Desired Characteristics:
- High School Diploma/GED or local equivalent
- 2 or more years of related manufacturing experience
- Experience in medical manufacturing or other highly regulated industry preferred.
- Local candidates will be given preference
- Ability to competently read, write, and speak in English
- Demonstrated basic computer skills and ability to navigate online instructions
Other: 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
- Knowledge and understanding of production process, work instructions, documentation configuration control, non-conforming & rework documentation requirements and operates within them to ensure that a device conforms to it’s specification.
- Aware of and comply with Stop Order, Concessions, ESD, Calibration, Preventative Maintenance, Material Identification & Segregation, and Good Documentation Practices, as associated with this job type/position
These jobs might be a good fit
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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
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
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.
These jobs might be a good fit
