Product Program Manager - Radiography Systems

GE Healthcare Private Limited

Bengaluru

On-site

INR 2,500,000 - 3,600,000

Full time

13 days ago

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Benefits offered by this job

Relocation Assistance Provided

Job summary

GE HealthCare is seeking a Product Program Manager for RAD subsystem products including X-Ray Tubes and X-Ray Generators. You will drive design changes, lifecycle management and reliability improvements across installed-base equipment.

You will partner with global cross-functional teams to ensure quality, regulatory compliance and timing of product introductions while leveraging data to set reliability targets and drive continuous improvement.

Qualifications

  • 8+ years of engineering experience in medical devices or highly regulated industries.
  • Experience in Installed Base Engineering, Engineering Change Management, Design Controls, Risk Management and Product Lifecycle Management.
  • Strong knowledge of DFMEA/PFMEA, Verification & Validation, design reviews and regulatory compliance (IEC 60601, ISO 13485, ISO 14971).
  • Proficiency in field performance monitoring, failure analysis and reliability data analysis.

Responsibilities

  • Own field and factory performance of RAD Tubes and Generators, focusing on quality, reliability, compliance, cost and delivery.
  • Lead investigations of field failures, including root cause analysis and corrective actions.
  • Collaborate with System Engineering, Field Engineering and Service teams for troubleshooting and resolution of field issues.
  • Support NPIs with reliability target setting and performance insights.
  • Represent Engineering during audits and drive design control documentation.

Skills

Field performance monitoring
Statistical data analysis
Failure analysis
RCA
Design for Reliability
Quality Management Systems
Regulatory compliance
Product lifecycle management
Engineering leadership

Education

Electrical and Electronics/Mechanical Engineering

Job description

Job Description

Product Program Manager RAD and Change Management Job Description Summary Lead Product Program Management for RAD subsystem products X-Ray Tubes and X-Ray Generators for mobile and fixed radiography systems. Drive Engineering design changes and Product Life Cycle Management for X-Ray Tubes and X-Ray Generators at GEBEL. Own installed-base product performance and drive improvements in quality, reliability, regulatory compliance, lifecycle, cost and delivery, while leveraging installed-base data to establish reliability targets and Design for Reliability for new product introductions. GE HealthCare is a leading global medical technology and digital solutions innovator. Our purpose is to create a world where healthcare has no limits. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world 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.

Key Responsibilities
  • Own field and factory performance of RAD Tubes and Generators, with focus on quality, reliability, compliance, cost and delivery.
  • Monitor field performance and Early Life Failure (ELF) trends using FoA, IPFR90 and IPFR180 metrics and represent product performance in global reviews.
  • Analyze field and reliability data using statistical methods, including Weibull analysis and B10/B50 life estimation, to identify risks and improvement opportunities.
  • Lead customer complaint and field failure investigations, including field-return autopsy, failure analysis, RCA, corrective actions and product fixes.
  • Partner with System Engineering, Field Engineering and Service teams for technical troubleshooting, product training and resolution of field issues.
  • Support NPIs with reliability target setting, leveraging installed-base performance, failure trends and reliability insights.
  • Support Risk Management activities, including DFMEA/PFMEA, design reviews, Verification & Validation and risk assessments.
  • Maintain Technical Files, Risk Management and Design Control documentation, ensuring QMS compliance and audit readiness.
  • Lead product lifecycle initiatives covering obsolescence, product improvements, regulatory compliance and Variable Cost Productivity (VCP).
  • Chair Engineering Change Control Board (ECCB) reviews and drive timely, technically rigorous and QMS-compliant engineering changes for X-Ray Tubes and Generators.
  • Serve as Engineering BPOC for Supplier Change Requests (SCRs), including initial impact assessment, cross-functional coordination and assignment of change owners.
  • Represent Engineering during QMS, regulatory, certification and customer audits, and support Quality Management Reviews.
  • Partner with Manufacturing, Quality, Regulatory, Service, Supplier Quality and Sourcing to improve product quality, manufacturing yield, reliability and cost.
  • Apply statistical methodologies to drive structured problem solving, RCA and continuous improvement.
Qualifications
  • Bachelor’s / Master’s / Phd in Electrical and Electronics/Mechanical Engineering discipline.
  • 8+ years of engineering experience, preferably in medical devices, medical imaging, X-Ray products or other highly regulated industries.
  • Experience in Installed Base Engineering, Engineering Change Management, Design Controls, Risk Management and Product Lifecycle Management.
  • Strong experience in field performance monitoring, failure analysis, RCA, reliability engineering and statistical data analysis.
  • Working knowledge of Weibull analysis, B10/B50 life estimation, reliability target setting and Design for Reliability.
  • Working knowledge of medical-device and X-Ray Tube/Generator product safety standards, QMS requirements and regulatory compliance, including applicable IEC 60601, ISO 13485 and ISO 14971 requirements.
  • Working knowledge of QMS and Design Control tools, including DFMEA/PFMEA, Risk Management, Design Reviews, Verification & Validation, ECR/ECO, CAPA and configuration/change management.
  • Experience with Supplier Change Management, obsolescence, product quality improvement and manufacturing/yield improvement.
  • Familiarity with structured problem-solving tools such as 5-Why, Fishbone, Pareto analysis and statistical analysis.
  • Six Sigma Green Belt certification preferred.
Desired Characteristics
  • Strong technical leadership, systems thinking and structured problem-solving skills.
  • Ability to translate field and reliability data into product improvements and NPI reliability targets.
  • Strong analytical, statistical and risk-based decision-making capability.
  • Ability to influence and collaborate effectively across global cross-functional teams.
  • Strong execution focus across quality, reliability, compliance, cost and delivery.
  • Excellent communication, stakeholder management and technical documentation skills.
  • Self-driven and results-oriented, with a strong focus on continuous improvement and execution excellence.
Inclusion and Diversity

GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership – always with unyielding integrity.

Additional Information
  • Relocation Assistance Provided: Yes
  • Experience Level: Mid Level
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