דרושים Clinical Data Integration Lead ב-Ge Healthcare ב-ארהב

Key Responsibilities:

• Lead projects to design and develop automation systems to enhance manufacturing productivity, new product introduction and capacity.
• Own the controls architecture and software for PLC, Robotics, and Vision Systems.
• Lead Design Transfer of NPIs by collaborating with manufacturing, manufacturing engineering, and product engineering teams.
• Identify high Return on Investment opportunities, design and conduct feasibility studies, and develop business cases to deploy automation into production.
• Apply creative solutions and ideas to drive productivity and quality using LEAN methodology, novel fixturing, collaborative robots, AI, traditional automation techniques, and integration of PLCs, HMIs, and motion systems.
• Support Brilliant Factory initiatives by connecting physical processes with digital information.
• Create standard automation Equipment/User Requirement Specifications to drive component standardization, data standards, and safety risk assessments.
• Manage projects and lead project teams in a matrix organization.
• Leverage and manage outside suppliers to deliver automation solutions.
• Troubleshoot factory equipment controls, update/debug control software and support factory equipment as needed.

Required:

• Bachelor’s Degree in Electrical, Mechanical, Manufacturing Engineering, or related technical degree.
• 3+ years’ experience in factory automation, deploying various automation technologies from concept phase through final implementation into production.
• Demonstrated skills in PLC and HMI programming, trouble shooting and debug
• Experience in program or project management skills of internal/external integrators.
• Experience developing technical documents, including the ability to write/perform FMEA’s, Equipment Risk Assessments, ERS’s (Equipment Requirements Specifications), and Validation Plans.
• Experience with design tools such as AutoCAD, SolidWorks, and CREO.

Desirable:

• 5+ years’ experience in the design, build, programming, and deployment of automation.
• Experience with Fanuc Robot Programming and Python code development.
• Experience with controls automation design and safety standards; NFPA 79, RIA15.06, and other relevant industry standards.
• Substantial industrial experience in Manufacturing Engineering.
• Six-sigma DMAIC & DFSS certified.
• Solid working knowledge of Medical Device QMS procedures.
• Experience working with global teams.
• Demonstrated experience owning production processes and growing capability in yield, quality, and capacity.
• Demonstrated troubleshooting, analytical, and planning skills.
• Strong communication skills (written and verbal) to all levels of the organization.
• Ability to identify and implement Best Practices.

• Development of repair and inspection technologies, process qualification, industrialization. Related program deliverables to repair facilities for new and updated processes.

• Developing in-depth knowledge of a technical discipline. Uses prior experience and acquired technical expertise to execute strategy.

• In-depth understanding of key business drivers; uses this understanding to accomplish own work. In-depth understanding of how work of own team integrates with other teams and contributes to the area.

• Uses some level of judgment and has ability to propose different solutions outside of set parameters but with guidance. Uses prior experience and on-the-job training to solve straightforward tasks. Has access to technical skills and analytic thinking required to solve problems. May use multiple internal sources outside of own team to arrive at decisions.

• A job at this level is likely to be an individual contributor with proven interpersonal skills or an early people leader who can hire and develop talent. Provides informal guidance to new team members.

• Bachelor's degree in a STEM (Science, Technology, Engineering, or Math) field from an accredited university or college.

• Minimum 6 years of work experience in product design and/or manufacturing.

• Minimum 3 years of process development experience including verification and validation.

• Ability and willingness to travel up to 20% of the time.

• 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.

• Strong oral and written communication skills.

• Demonstrated ability to analyze and resolve technical problems.

• Ability to document, plan, market, and execute programs.

• Experience medical ultrasound probe design, manufacturing, or repair/refurbishment including familiarity with associated product quality requirements.

• Demonstrated facilitation, negotiation, and conflict resolution skills in driving closure on decisions and issues.

• Familiarity with ISO, FDA, and other regulatory standards.

• Experience with entire product lifecycle of GE HealthCare products, including experience with GE HealthCare systems such as: MyWorkshop, Oracle, Quality Management System, etc.

• Oversight and management of front-line manufacturing employees. Typically managing hourly employee populations.

• Developing in-depth knowledge of a technical discipline. Uses prior experience and acquired technical expertise to execute policy/strategy.

• In-depth understanding of key business drivers; uses this understanding to accomplish own work. In-depth understanding of how work of own team integrates with other teams and contributes to the area.

• Uses some level of judgment and has ability to propose different solutions outside of set parameters but with guidance. Uses prior experience and on-the-job training to solve straightforward tasks. Has access to technical skills and analytic thinking required to solve problems. May use multiple internal sources outside of own team to arrive at decisions.

• A job at this level is likely to be an individual contributor with proven interpersonal skills or an early people leader who can hire and develop talent. Provides informal guidance to new team members

• Bachelor’s Degree with three years production, supply chain experience or leadership, or High School diploma/GED and 7 years production or supply chain experience, or GE Leadership Program employee or graduate.

• Demonstrated ability to lead and develop teams.

• Prior experience with leading teams.

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.

GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).

• Implement and execute GEHC EHS programs / processes and maintain site-specific EHS documentation and plans

• Provide guidance and interpretation of EHS regulations and requirements

• Partner with global EHS team to manage site EHS compliance activities (inspections, training, monitoring, sampling, etc.)

• Drive EHS compliance through audits, process / equipment reviews and site inspections

• Lead site injury and illness prevention program. Lead incident / accident investigations and develop corrective & preventive action plans

• Lead site risk elimination/risk reduction activities

• Individuals located at manufacturing sites and fixed facilities that provide day-to-day EHS support for that facility

• Developing in-depth knowledge of a technical discipline. Uses prior experience and acquired technical expertise to execute policy/strategy

• In-depth understanding of key business drivers; uses this understanding to accomplish own work. In-depth understanding of how work of own team integrates with other teams and contributes to the area

• Uses some level of judgment and has ability to propose different solutions outside of set parameters but with guidance. Uses prior experience and on-the-job training to solve straightforward tasks, Has access to technical skills and analytic thinking required to solve problems. May use multiple internal sources outside of own team to arrive at decisions.

• A job at this level is likely to be an individual contributor with proven interpersonal skills or an early people leader who can hire and develop talent. Provides informal guidance to new team members

• Bachelor's degree from an accredited university or college with 5+ years of experience in EHS

• Experience managing sites that are VPP certified

• Experience managing hazardous waste and other environmental programs

• Advanced computer skills, primarily with MS Office software programs, i.e., Excel and PowerPoint

• Proven project and program management skills

• 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

• Hands on and proactive approach

• Leadership skills

• Use critical thinking skills and disciplined approaches to help others to resolve issues

• Able to successfully work in a fast pace, high pressure and dynamic environment

• Able to work closely with site management team and external resources

• Strong oral and written communication skills. Demonstrated ability to analyze and resolve problems. Ability to document, plan, market, and execute programs. Established project management skills.

What You’ll Do:

• Builds understanding of Customer’s existing clinical environment, needs, and goals for MIM Implementation

• Lead minor workflow adjustments and configurations, coordinate more complex workflow modifications through the appropriate channels to optimize system performance.

• Coordinates and manages workflow testing

• Creates and manages training and rollout plan(s)Is responsible for customer training and go-live support

• Relays any and all customer complaints and feedback to the appropriate MIM team(s) to ensure that they are reviewed and addressed in a timely manner.

• Supports technical sales for potential customers, and acts as a salesperson for MIM Software at the technical exhibition of medical conferences.

• Continuing medical and technical education is received by working with the staff at institutions and observing exhibitions at medical conferences.

• Participate in on-the-job training within a hospital environment to gain firsthand experience of clinical workflows and challenges.

• Facilitate training sessions for team members, along with cross-functional teams.

• Travel up to 60% of the time for on-site customer training, offering an exciting opportunity to work in diverse settings while directly impacting customer success.

What You’ll Need:

• A background as nuclear medicine technologist or in a support capacity for nuclear medicine procedures preferred

• Must have strong interpersonal communications skills, project organizational skills, problem-solving abilities, as well as the aptitude to develop a clinical and technical knowledge base.

• 3-5 years of clinical or medical experience is preferred

• At least a four-year bachelors’ degree program from an accredited university, preferably in a technical field or relevant experience is preferred

• The ability to travel on an as-needed basis, no more than 60% of the time

• Vaccination is required

What You’ll Get:

• Hybrid work environment so you can work remotely as well as enjoy the office

• Permissive time off

• A 401(k) with a 4% match

• Tuition reimbursement programs

• Relaxed office setting where jeans are the norm

• Free snacks and beverages at the office

• 24-hour access to an in-office fitness center

Roles and Responsibilities

• Provide oversight to large suppliers or Business Process Outsourcing. Ensure Business Process Outsourcing compliance with SLAs and act as the primary point of contact on all service level issues and resolution.
• Developing in-depth knowledge of a discipline. Uses prior experience and acquired expertise to execute functional policy/strategy.
• A job at this level is likely to be an individual contributor, with proven interpersonal skills. Communication with direct colleagues and the business about design and coordination services rendered. Provides informal guidance to new team members. Explains complex information to others in straightforward situations.
• Impacts projects, processes and procedures in own field. The role operates with some autonomy, but is focused on execution of activities/provision of advice within an enabling discipline covered by standard functional practices and procedures. Activities require professional judgment, but may require more senior levels of guidance.
• Utilizes technical expertise and judgement to solve problems. Leverages technical skills and analytic thinking required to solve problems. May use multiple internal sources outside of own team to arrive at decisions.
• Domestic and International Travel may be required up to 20% of the time

Required Qualifications

• Bachelor's degree.
• 4+ years of experience in Sourcing, Supply Chain, Procurement, Project Managment or related field.

Desired Characteristics

• Strong oral and written communication skills.
• Demonstrated ability to analyze and resolve problems.
• Ability to document, plan, market, and execute programs.
• Established project management skills.

Roles and Responsibilities

• System Architecture & Design: Lead the development of system and architecture and design, including system-level requirements and interface specifications

• Integration & Performance: Oversee integration of subsystems to ensure optimal image quality, patient safety, and system reliability; Drive system-level performance analysis and trade-off studies.

• Technical Leadership: Serve as the technical point of contact for cross-functional teams including hardware, software, clinical applications, and regulatory affairs; Mentor junior engineers and contribute to technical reviews and design decisions; Lead risk assessments and failure mode analyses (FMEA) for system-level concerns.

• Lifecycle Management: Support product development from concept through commercialization and sustaining engineering; Lead system verification and validation planning and execution; Ensure compliance with medical device regulations (e.g., FDA, IEC 60601).

• Stakeholder Collaboration: Translate customer and clinical needs into system requirements and design inputs; Work closely with product management, marketing, and service teams to ensure product success; Interface with external partners and suppliers as needed.

Required Qualifications

• Bachelor’s or Master’s degree in Electrical Engineering, Biomedical Engineering, Physics, or related field (PhD preferred).

• 3+ years of experience in systems engineering, preferably in medical imaging or MRI.

• Strong understanding of MRI physics, system components, and clinical workflows.

• Proficient in the use of software tools for analysis and simulation.

• Experience with regulatory standards and design controls for medical devices.

• Excellent communication, analytical, and problem-solving skills.

Desired Characteristics

• Experience with MRI system modeling, simulation, or performance optimization tools.
• Familiarity with advanced imaging techniques (e.g., diffusion, spectroscopy, functional MRI).
• Hands-on experience with MRI hardware or software development.
• Knowledge of signal processing and image reconstruction algorithms.
• Experience working in Agile or hybrid development environments.
• Prior involvement in clinical trials or collaboration with radiologists and technologists.
• Strong background in risk management and safety-critical systems.
• Experience with international regulatory submissions (e.g., CE Mark, MDR).