Production Associate jobs at Ge Healthcare in United States, Salt Lake City

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.

The Production Maintenance Technician would provide daily process support, troubleshooting, preventative maintenance, and repair of flat panel The Production Maintenance Technician would provide daily process support, troubleshooting, preventative maintenance, and repair of flat panel manufacturing equipment. The GE Healthcare facility located in North Greenbush, NY is a 230,000 sf facility built for the manufacturing of Digital X-ray detectors. The facility houses 60,000 sf of cleanroom environments built for high tech manufacturing. The process equipment consists of High Vacuum Equipment, Photolithography Equipment, Wet Chemistry Processing, Electrical Testing Equipment, and Chemical Plating Equipment. The position will have daily responsibilities for equipment preventative maintenance, repair of processing equipment, and continuous equipment optimization.
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.

Required Qualifications

• 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

Desired Qualifications

• 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.

Description: Responsible for directing the day-to-day work in the assigned area. Individual may provide input or recommendations to supervisory personnel on hiring, performance assessment and discipline. Responsible for execution of the daily, weekly, and monthly forecasted production priorities required to meet output quotas and group performance goals.

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.

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.Job Description

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

Production Associate on the Mainframe line Salt Lake City, UT. Employee will help to assemble Elite C-Arm systems on the Salt Lake City Mainframe line. Employee will do so by following work instructions and using tools including torque tools, battery operated torque guns, hand tools, and force gauges. Employee will also take part in safety and other projects as necessary.
Essential Responsibilities

• Perform entry to mid-level manufacturing/assembly operations on our production line and other various tasks following procedures, work instructions, and process aid sheets.

• Use lift platforms, hoist, torque tools, and other power hand tools to assemble our X-ray machines.

• Read and follow work procedures, receive verbal instructions regarding duties to be performed.

• Maintain daily production output.

• Cross train and work in multiple functions for business flexibility.

• Follow all EHS and Quality policies and procedures.

• May participate in quality control inspections.

• Work 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.

• Comply with EHS regulations and policies.

• Comply with attendance policies and be willing to work voluntary overtime when needed.

• Able to see small assembly parts

Required Qualifications

• High School Diploma/GED or equivalent or 6 months of line manufacturing experience with mechanical or electromechanical assembly.

• Ability to communicate, receive and understand instructions regarding duties.

• Demonstrated attention to detail and quality-minded work habits.

• You must be willing to work out of our office located in Salt Lake City, Utah daily, Monday - Friday.

Desired Characteristics

• Minimum of 2 years of related manufacturing experience.

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

• Demonstrated basic computer skills and ability to navigate online instructions.

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.Job Description

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