Jobs at Ge Healthcare

Key Responsibilities:

• Design and implement automated systems including robotics, PLCs, HMIs, and vision systems to support medical device production.
• Lead the development and validation of automated equipment in compliance with internal quality systems
• Collaborate with Design Engineering, Quality, and Manufacturing teams to ensure automation solutions align with product and process requirements.
• Generate and maintain documentation such as ERS, FAT/SAT protocols, Equipment Qualifications, and risk assessments.
• Lead equipment qualification and process validation activities.
• Drive continuous improvement initiatives focused on safety, quality, and efficiency.
• Troubleshoot and resolve issues with automated systems and provide technical support to production teams.
• Stay current with emerging automation technologies and regulatory requirements.

Qualifications:

• Bachelor’s degree in Electrical Engineering, Mechanical Engineering, Mechatronics, or a related field.
• 3+ years of experience in automation engineering, preferably in medical device or pharmaceutical manufacturing.
• Proficiency in PLC programming (e.g., Omron, Allen-Bradley, Siemens), robotics integration, and industrial communication protocols (e.g., OPC UA, Modbus, Ethernet/IP). and HMI development.
• Experience with automated inspection systems (e.g., machine vision, laser measurement, 3D scanning).
• Experience with Python, C/C++, or MATLAB for automation scripting and data analysis. Familiarity with GMP, FDA regulations, and ISO standards.
• Strong analytical, documentation, and problem-solving skills.
• Excellent communication and cross-functional collaboration abilities.
• Experience with MES and SCADA systems.

Preferred Qualifications:

• Experience with cleanroom automation.
• Knowledge of data integrity principles and electronic records.
• Lean Six Sigma certification or experience with process improvement methodologies.

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.

• Responsible for leading daily operations within the distribution center, ensuring compliance with safety and quality standards while driving continuous improvement and cost-effective practices

• Provides direct supervision to Distribution personnel, ensuring timely execution of distribution plans and achievement of operational milestones including manufacturing & logistics schedules

• Champions a culture of safety, compliance, accountability, and LEAN

• Identifies and implements process improvements to enhance service levels, reduce operational costs, and support overall business objectives

• Oversee daily operations, including scheduling, issue resolution, and multiple shifts (weekends)

• Collaborate/partner with internal and cross-functional teams

• Analyze trends/supply chain strategies, conduct required analysis that support financial and capital planning/improvements, recommend initiatives/tactics to meet business growth and financial objectives.

• Manages departmental goals and KPI’s, ability to both conduct analysis and lead teams to conduct analysis

• Baseline warehousing and distribution network cost structure and capacity utilization

• Use data and structured tools to identify and address performance gaps

• Lead cross-functional projects and allocate resources effectively

• Use problem-solving tools (e.g., fishbone diagrams, Pareto analysis) to identify and address quality/performance gaps

• Gain a comprehensive understanding of our supply chain including manufacturing, distribution, partners, customers, baseline of product flow and seasonality, detailed operating costs, key supply chain processes in sourcing, planning, and operations.

• Profile/articulate supply chain processes and inventory flows throughout the network (end to end)

• Analyze network optimization opportunities for cost, inventory, and service delivery

• Optimize inventory flow through network (e.g. ship from DC vs. ship from stores; partner drop ship options; optimal stocking positions and storage footprint

• Develop high-level planning models to support inventory optimization across supply chain networks

• Assess inventory planning processes and systems and recommend potential improvement opportunities for optimizing service levels and inventory turns

• Develop transformation plans to drive proposed changes in transportation, freight optimization, warehousing & distribution

• Implement and oversee the quality of deliverables and effectively manage the team and day-to-day targets and relationships to ensure exceptional on time performance

• Bachelor’s degree in Logistics, Supply Chain Management, Engineering or related field.

• 2–5+ years of operational experience in logistics, distribution, or supply chain management

• Prior supervisory experience

• Experience working in a regulated healthcare (FDA, cGMP) environment

• CSCP and/or CLTD certification

• Established project management skills.

• Experience with SAP/WM

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.

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.

• 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.

Key responsibilities/essential functions include

• Performs required analytical testing on in-process and final products.
• Testing using HPLC, FTIR, ICP-OES, UV/VIS, Liquid Scintillation, and Gamma Spectrometer.
• Participates in the performance of investigations of OOS results.
• Tracking and trending of analytical data.
• Participates in validation projects requiring analytical support.
• Contributes to process improvement through Lean and 5S.
• Assists in the stocking and supplying of the QC lab.
• Performs visual inspection of finished product.

Quality Specific Goals:

• Knowledge and understanding of acceptance activity requirements for incoming, in-process, and final inspection requirements (as associated with job type/position) to ensure the product conforms to its specification and out of specification items are properly handled.
• Basic knowledge and understanding of Stop Orders, Concessions, CAPA, Calibration, Preventative Maintenance, Material Identification & Segregation, documentation configuration control practices; documentation & disposition of non-conforming material, and Good Documentation Practices requirements, Part 11 compliance as associated with this job type/position
• 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

Required Qualifications:

• Bachelor’s degree in chemistry (preferred) or related science field.
• Proficient with software applications applicable to the job.
• Must be available for nights and weekends as needed.
• Must have the ability to distinguish color.
• Ability to lift 25lbs

Preferred Qualifications:

• Waters Empower Experience or similar software.
• Equipment experience with HPLC, ICP, UV/Vis, FT-IR.
• Experience working with radioactive material including the use of gamma spectrometers, Ion Chambers and liquid scintillation analyzers.
• Visual inspection experience Working knowledge of USP Experience in a FDA regulated QC environment
• Background in Math or Chemistry

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

• Safety: Owns all safety metrics for the department including continuous improvement to drive risk reduction & injury prevention.
• Quality: Leverage Lean Six Sigma mindset to deliver product quality improves resulting in scrap reductions and better field quality.
• Delivery: Responsible for on-time delivery and inventory of department.
• Cost: Deliver financial results aligned with productivity targets and budget. Own productivity roadmap to delivery sustained YoY improvements.
• People: Foster a culture focused on people development.
• Work cross-functionally with QA, AME, and Engineering teams to deliver department/site goals.
• Lead compliance efforts in support of plant goals.

Required Qualifications

• Bachelor’s Degree with 5 years production/supply chain leadership.
• Demonstrated ability to lead and develop teams.
• Demonstrated ability to identify/implement best practices and deal with high levels of ambiguity

Desired Characteristics

• Experience working in regulated industry
• Design or manufacturing engineering experience
• Functional manager experience