דרושים Lead Electrical Engineer ב-Ge Healthcare ב-United States, Aurora

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.

Roles and Responsibilities

• Fosters a Quality culture by leading quality and compliance activities for innovative, leading-edge MR Coil technologies within the areas of design and development, design transfer, manufacturing, and service.
• Ensures adherence to GE HealthCare QMS and regulatory requirements (e.g. 21 CFR 820, ISO 13485, MDSAP) while driving process effectiveness and efficiency. Ensures plans, protocols, results, and conclusions are generated, reviewed, and approved according to applicable procedures.
• Represents GE HealthCare to external regulatory agencies and drives audit readiness.
• Performs internal audits to ensure quality standards and regulatory requirements are addressed.
• Ensures quality of CAPA (Corrective and Preventive Action) projects, including robust root cause investigations, and nonconformance evaluations.
• Support successful product launch of design and manufacturing transfers.
• Apply Lean methodologies to solve problems, improve daily work, and simplify processes.
• Support analysis and execution to achieve Quality objectives and priorities.

Required Qualifications

• Bachelor's degree from an accredited university or college (or a high school diploma / GED with at least 6 years of relevant work experience)
• At least 3 years of relevant experience in Quality Assurance, Quality Engineering or Design Controls in a regulated industry, Medical Device experience preferred
• Demonstrated understanding of Medical Device Quality Management System requirements and regulatory requirements including but not limited to FDA CFR 21 820 and ISO 13485.
• Demonstrated knowledge of Quality and Process Improvement tools.
• Legal authorization to work in the U.S. is required. Sponsorship for employment visas, now or in the future, for this job opening is not available.

Desired Characteristics

• Experience in New Product Introduction of Medical Devices, including Design Controls, Production and Process Controls, and Installation and Servicing.
• Experience with applying the GE HealthCare Quality Management System in New Product Introduction programs.
• Strong technical aptitude
• Influencing skills and ability to clearly communicate the requirements of Design Controls, Design Verification and Validation, Production and Process Controls, Corrective & Preventive Action (CAPA), and Risk Management across functions.
• Demonstrated ability to collaborate effectively and resolve conflicts.
• Critical thinking, problem solving, root-cause analysis, and process improvement skills.
• Excellent interpersonal and leadership abilities.
• Proficiency in managing multiple priorities effectively.

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.

• Lead projects to design and develop automation systems to enhance manufacturing productivity.

• Influence product design to incorporate automation standards in NPI projects.

• Lead Design Transfer of NPIs by collaborating with manufacturing, manufacturing engineering, and product engineering teams.

• Identify high ROI applications, design and conduct feasibility studies, and 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.

• Manufacture solutions using machining equipment and collaborate with vendors on machine builds.

• 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.

• Bachelor’s Degree in Electrical/Automation, Mechanical, Manufacturing Engineering, or related technical degree. From an accredited college/university.

• Minimum 3 years’ experience in using, applying, and deploying various automation technologies from concept phase through final implementation into production.

• Demonstrated program or project management skills of internal/external integrators.

• Demonstrated experience owning production processes and growing capability in yield, quality, and capacity.

• 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.

• Demonstrated troubleshooting, analytical, and planning skills.

• Strong communication skills (written and verbal) to all levels of the organization.

• Minimum 5 years’ experience in the design, build, programming, and deployment of automation.

• Ability to identify and implement Best Practices.

• Experience in controls, PLC programming, and Robot Programming.

• Substantial industrial experience in Mechanical or Manufacturing Engineering.

• Six-sigma DMAIC & DFSS certified.

• Solid working knowledge of Medical Device QMS procedures.

• Experienced in developing tools and templates.

• Experience working with global teams.

Roles and Responsibilities

• Includes both Supplier Quality Assurance and Supplier Quality Development. Includes supplier qualifications, action plans, audits, performance monitoring, and assisting key suppliers towards industrial standards of excellence. SQEs have various levels of differentiation which are related to level of technical understanding of engineering drawings and ability to manage vendors.
• 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.

Required Qualifications

• Bachelor's degree from an accredited university or college (or a high school diploma / GED with at least 6 years of experience)
• Minimum of 3 years of work experience with technical depth/knowledge in supplier quality and development
• 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 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.

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

Duties include (but are not limited to):

• Designing new products and/or supporting Installed Base of Analog, RF, and/or Digital electrical circuit boards, components and interconnects
• Working with patient/customers and/or technical leadership to ensure that the technical deliverables are consistent with the goals of larger programs, projects or initiatives
• Leading design efforts with Electrical CAD and Simulation tools (Cadence, ADS, etc.)
• Executing design to engineering standards
• Working within a team to deliver technical solutions
• Defining and executing component design verification
• Seeking mentoring to learn and solve problems
• Engaging in all phases of product development and support, including concept, architecture, documentation, design, prototype, test, supplier interfaces, manufacturing introduction and service support
• Developing and maintaining product quality and engineering project funnel
• Conducting analysis of installed base and new product reliability
• Team-oriented collaborator with solid communication skills

Required Qualifications

• BS in Electrical Engineering or related degree with 5+ years of relevant experience, or a Masters Degree with 3+ years of experience
• Knowledge of standard drafting practices, product structuring, electronics modeling and drawing practices, and engineering analysis techniques.
• Knowledge of Analog and RF circuit design
• Understanding of engineering product development processes

Desired Characteristics

• Master’s degree with 8+ years of experience in electrical engineering
• Medical device experience
• Demonstrated experience in the following: Electromagnetics, Transmission Line design, Antenna Theory & Design, Mixers, Oscillators, Amplifiers, Analog Design, RF Printed Circuit Board Layout experience
• Experience with Lean methodologies, 5S, Kaizen etc.
• Experience with Medical device standards like IEC60601-1
• Experience with Weibull Analysis and DFR (Design for Reliability) tools
• Self-starter, energizing, results oriented, and able to multi projects

Not open to Sponsorship or OPT for this role

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).