Full-Time

Lead Manufacturing Process Engineer

AME & Testing

Updated on 9/13/2026

GE Healthcare

GE Healthcare

1-10 employees

Imaging, monitoring, and healthcare IT solutions

No salary listed

Bengaluru, Karnataka, India

In Person

Relocation assistance is provided.

Bachelor's, Master's

Category
Manufacturing & Process Engineering (1)
Required Skills
Power BI
Six Sigma
Data Visualization
Machine Learning
Data Analysis

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Requirements
  • A Bachelor’s or Master’s degree in Mechanical Engineering, Production Engineering, Manufacturing Engineering, Mechatronics, Robotics & Automation Engineering, Electrical Engineering, Electrical & Electronics Engineering, or a related engineering discipline.
  • A minimum of 6+ years of relevant experience in Process Engineering, Manufacturing Engineering, Advanced Manufacturing Engineering, Test Engineering, Automation Engineering, or a related core engineering environment.
  • Strong hands-on experience in manufacturing or process engineering, including manufacturing process development, equipment development, troubleshooting, and continuous improvement.
  • Hands-on experience with test equipment automation and automated manufacturing or testing systems.
  • Hands-on exposure to Special Purpose Machines (SPMs), including development, implementation, operation, integration, or troubleshooting.
  • Practical understanding of electromechanical equipment and components, including servo motors, encoders, ball screws, sensors, electrical and electronic circuits, and equipment control systems.
  • Knowledge or hands-on experience with NI hardware programming, hardware interfaces, or comparable equipment control systems used to integrate hardware and software for automated machine or test functions.
  • Strong problem-solving, troubleshooting, root cause analysis, and failure analysis capabilities.
  • Knowledge and practical application of structured problem-solving and continuous improvement methodologies such as Lean Manufacturing, Six Sigma, and data analysis.
  • Exposure to Power BI, AI tools, IoT platforms, advanced analytics, or similar digital manufacturing technologies.
  • Understanding of predictive maintenance concepts, equipment data analysis, sensor-based monitoring, and data-driven decision-making.
  • Experience or working knowledge of manufacturing process and equipment qualification and validation.
  • Knowledge of Quality Management System (QMS) requirements applicable to regulated manufacturing environments.
  • Prior experience providing technical guidance or managing a small team, with experience supporting approximately two or more team members, contractors, or trainees.
  • Strong focus on engineering documentation and the ability to develop clear technical reports, specifications, validation documentation, and manufacturing records.
  • Ability to manage multiple technical priorities and deliver commitments on time while maintaining quality and compliance requirements.
Responsibilities
  • Own and lead manufacturing engineering activities for New Product Introductions (NPI) and manufacturing transfers for existing products, collaborating with global and local cross-functional teams including Engineering, Manufacturing, Quality, and Supply Chain.
  • Lead and support process engineering activities associated with new product introductions, manufacturing readiness, production ramp-up, and implementation of new manufacturing and testing technologies.
  • Design, develop, improve, and support manufacturing automation systems, test equipment, Special Purpose Machines (SPMs), fixtures, tooling, and manufacturing aids to enable efficient and reliable production.
  • Support the transition from legacy testing systems to new testing platforms, software, automation tools, and testing infrastructure.
  • Develop and support automated test equipment involving electromechanical components and control systems, including servo motors, encoders, ball screws, sensors, electrical and electronic circuits, and related machine control technologies.
  • Apply knowledge of NI hardware programming and equipment control systems to support automated equipment functions such as motor control, operational sequencing, equipment run-time management, sensor integration, data capture, and automated machine operations.
  • Lead troubleshooting and structured problem-solving activities to resolve complex medical equipment manufacturing and testing issues.
  • Conduct root cause investigations and failure analysis to identify technical issues related to equipment, manufacturing processes, test systems, and product performance, and implement sustainable corrective actions.
  • Own process qualification and validation of manufacturing processes, assembly-line tools, automation systems, and testing equipment to ensure robust and compliant manufacturing operations.
  • Lead process risk assessments and drive factory, forward production, and field quality improvements through structured problem-solving, failure analysis, and Defects Per Unit (DPU) reduction initiatives.
  • Champion Lean Manufacturing, automation, digital transformation, AI/ML, IoT, advanced analytics, and plant modernization initiatives in collaboration with central Advanced Manufacturing Engineering teams to improve operational excellence and productivity.
  • Utilize Power BI and other appropriate data visualization and analytics tools to support equipment performance monitoring, manufacturing reporting, data analysis, and data-driven decision-making.
  • Support the collection and analysis of manufacturing and equipment data to identify trends, understand equipment behavior, improve testing processes, and identify opportunities for productivity and quality improvement.
  • Support the development and implementation of predictive maintenance approaches using equipment, sensor, and performance data to identify potential failures and enable a transition from reactive to data-driven maintenance strategies.
  • Evaluate opportunities to apply AI/ML and advanced analytics to manufacturing and testing processes where these technologies can improve equipment performance, testing effectiveness, product quality, productivity, or engineering decision-making.
  • Collaborate with internal and external stakeholders on equipment upgrades, new testing infrastructure, manufacturing technology implementation, and continuous improvement initiatives.
  • Manage engineering change requests and lead the effective implementation of approved changes on the manufacturing floor, including appropriate documentation and process updates.
  • Support implementation and execution of Quality Management System (QMS) requirements on the manufacturing floor in accordance with applicable medical device regulations and internal quality requirements.
  • Develop and maintain clear engineering documentation, equipment and process specifications, validation records, technical reports, work instructions, and other manufacturing process documentation.
  • Provide technical leadership and coaching to Process Engineering team members in automation, process development, test equipment, risk analysis, structured problem-solving, and QMS requirements.
  • Initially operate as an individual contributor while providing guidance and oversight to contractors and graduate trainees (GTs), with the potential to take on increased team leadership responsibilities as the organization and program grow.
  • Support and guide small engineering teams, contractors, or trainees to ensure technical activities are executed effectively and aligned with program, quality, and delivery expectations.
  • Manage multiple engineering priorities and deliver technical solutions on time while maintaining appropriate standards of quality, documentation, and regulatory compliance.
Desired Qualifications
  • Strong written and verbal communication skills with the ability to work effectively across Engineering, Manufacturing, Quality, Supply Chain, and other cross-functional teams.
  • Experience in medical device or medical equipment manufacturing.
  • Experience supporting New Product Introduction (NPI), product industrialization, manufacturing transfer, production ramp-up, or similar product introduction programs.
  • Experience working with complex medical equipment, capital equipment, or other highly engineered electromechanical products.
  • Knowledge of PCB/electronics-related manufacturing, assembly, and testing.
  • Experience supporting equipment upgrades or transitioning from legacy manufacturing/test equipment to new automated testing platforms.
  • Experience applying Power BI or similar visualization tools to manufacturing, equipment, test, or operational data.
  • Exposure to AI/ML-enabled manufacturing applications, IoT technologies, connected equipment, or advanced manufacturing analytics.
  • Experience implementing or supporting predictive maintenance solutions using equipment, sensor, or operational data.
  • Experience with manufacturing data collection, performance monitoring, reporting, and continuous improvement.
  • Experience leading process risk assessments, manufacturing quality improvements, DPU reduction, and product reliability improvement initiatives.
  • Experience collaborating with global Advanced Manufacturing Engineering, product engineering, manufacturing, quality, and supply chain teams.
  • Demonstrated ability to mentor engineers, graduate trainees, technicians, or contractors and build technical capability within a manufacturing organization.
  • Ability to adapt to evolving technologies, new manufacturing platforms, and changing program requirements while maintaining a strong focus on execution, quality, and compliance.

GE Healthcare Systems provides medical technologies and digital infrastructure to improve diagnosis, treatment, and monitoring of patients. Its products include imaging systems, mobile diagnostic devices, patient monitoring tools, and healthcare IT software that work together as hardware, software, and services to support hospitals, clinics, and researchers. The company differentiates itself with a large, integrated ecosystem, strong focus on AI analytics, and a global service network backed by substantial R&D investment. Its goal is to improve patient outcomes and the efficiency of healthcare delivery by enabling accurate diagnoses, effective treatments, and scaled operations.

Company Size

1-10

Company Stage

IPO

Headquarters

Chicago, Illinois

Founded

1892

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Simplify Jobs

Simplify's Take

What believers are saying

  • Photonova Spectra won CE Mark on August 31, 2026, opening Europe sales.
  • Q2 2026 orders rose 11.1%, with 1.15x book-to-bill and record backlog.
  • Vivid cardiovascular ultrasound and ABUS breast screening launches broaden 2026 revenue opportunities.

What critics are saying

  • Patient Care Solutions revenue fell 13.5% in Q2 2026; management is reviewing a sale.
  • Jay Saccaro left in August 2026; William Grogan starts September 14, 2026.
  • If PCS recovery slips into 2027, GE HealthCare becomes a slower-growth imaging vendor.

What makes GE Healthcare unique

  • Photonova Spectra’s Deep Silicon CT differentiates GE HealthCare with photon-counting imaging.
  • GE HealthCare spans imaging, pharma diagnostics, ultrasound, and monitoring across hospital workflows.
  • The July 2026 backlog of $23.9 billion reflects sticky installed-base demand and services.

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Benefits

Health Insurance

Dental Insurance

Vision Insurance

Life Insurance

Disability Insurance

401(k) Retirement Plan

401(k) Company Match

Tuition Reimbursement

Relocation Assistance

Company News

Yahoo Finance
Sep 1st, 2026
GE HealthCare secures CE mark for Photonova Spectra photon-counting CT system

GE HealthCare has received CE mark approval for its Photonova Spectra photon-counting computed tomography system, enabling commercial sales in markets recognising CE marking. The clearance follows US Food and Drug Administration approval and Japanese regulatory clearance in March 2026. The system uses GE HealthCare's Deep Silicon detector technology to deliver ultra-high definition spectral and spatial imaging. It processes data volumes up to 50 times greater than conventional CT systems, utilising Nvidia's accelerated computing platform. Clinical collaborations are underway at UZ Brussel in Belgium and Rigshospitalet in Denmark to evaluate the system across cardiology, neurology, oncology and musculoskeletal imaging. The CE mark follows more than $5 billion in innovation investment by GE HealthCare.

Yahoo Finance
Aug 31st, 2026
Vertex Pharmaceuticals shows promise while GE HealthCare and Wells Fargo face challenges

Vertex Pharmaceuticals has emerged as a standout S&P 500 stock, according to StockStory's analysis. The company, which focuses on developing transformative medicines for serious diseases including cystic fibrosis and sickle cell disease, boasts a market capitalisation of $137.3 billion. Meanwhile, StockStory recommends avoiding two large-cap stocks. GE HealthCare, spun off from General Electric in 2023, faces concerns over stagnant organic revenue growth and declining operating margins. The medical equipment provider has a market cap of $32.4 billion. Wells Fargo also made the avoid list. The diversified financial services company, with a $262.2 billion market cap, has seen its net interest margin shrink by 33.6 basis points over two years, suggesting increased competition or declining loan profitability.

Associated Press
Aug 28th, 2026
GE HealthCare launches three new Vivid cardiovascular ultrasound systems for diverse care settings

GE HealthCare has introduced three new cardiovascular ultrasound systems to its Vivid portfolio: Vivid Explorer 1, Vivid Advanced 1, and Vivid Focus 1. The systems were unveiled at the European Society of Cardiology Congress 2026 in Munich, Germany. Each system targets different clinical settings whilst sharing a common technology foundation with the ultra-premium Vivid Pioneer. Vivid Explorer is designed for high-volume echo labs, Vivid Advanced for mid-size hospitals and cardiology practices, and Vivid Focus for everyday cardiac imaging. All three systems use cSound imaging technology and include AI-enabled automation tools to streamline echo workflows. The systems have received CE Mark approval but are awaiting US FDA 510(k) clearance and are not yet available for sale in the United States.

Yahoo Finance
Aug 3rd, 2026
GE HealthCare launches Invenia ABUS Prime and StreamVue for breast cancer screening

GE HealthCare has launched Invenia ABUS Prime and ABUS StreamVue, expanding its breast imaging portfolio with solutions for supplemental screening in women with dense breasts. The Invenia ABUS Prime system has been installed at BeSound in Los Angeles, marking one of the first US installations. ABUS StreamVue is a browser-based reading solution enabling remote exam review across imaging networks. The system received FDA 510(k) clearance and CE Marking. Studies show 40% of women have dense breasts, carrying four to six times higher breast cancer risk. Research indicates mammography may miss one-third of cancers in dense breasts. Invenia ABUS Prime features AI-enabled tools including Scan Quality Assessment and can increase scan speed by up to 40%. The AI Assistant has demonstrated a 33% reduction in reading time.

Yahoo Finance
Jul 29th, 2026
GE HealthCare Q2: Orders up 11%, backlog hits record $23.9B amid Patient Care struggles

GE HealthCare Technologies reported second-quarter results with orders rising 11% year-over-year and backlog reaching a record $23.9 billion. Revenue grew 3.5% organically to $5.3 billion, driven by Advanced Imaging Solutions and Pharmaceutical Diagnostics, which posted organic growth of 5% and 14.6% respectively. Patient Care Solutions remained weak, with revenue falling 13.5% due to component shortages and fulfilment problems. Management is reviewing strategic options for the segment, including a potential sale. The company maintained its full-year outlook of 3–4% organic sales growth, adjusted earnings per share of $4.80–$5.00, and approximately $1.6 billion in free cash flow. CFO Jay Saccaro is departing, with George Newcomb serving as interim CFO.