

Your role:
Quality Control and Improvement:
- Support MQ and SQE to conduct incoming failure parts analysis.
- Work with quality team to fulfil QMS requirement and support TUV, CFDA, and FDA audit.
Line Sustaining:
- Update WI and DHR according to ECR from designer or PPC.
- Daily NC analysis, find root cause and drive improvement.
- Support change controller to execute ECO in production on time and minimize the line interruption.
- Introduce new product / new process / new part in production.
LEAN and Cost Reduction:
- Continuously improve production efficiency by standardized work, line balance and automation project.
- Optimize production process and eliminate waste using lean method and tools.
- Organize and lead the lean activities and other improvement project.
Equipment Trouble Shooting and Improvement:
- Familiar with electrical test platform.
- Identify opportunities to improve current equipment or create new equipment and work with R&D or supplier to realize the requirement.
- Define the URS to guide new equipment purchasing and the equipment qualification.
- Define the gauge calibration requirement.
You're the right fit if:
B.S. or above in electrical, electronic engineering.
Familiar with AC, DC design and tuning.
Experience of X-ray testing is preferred.
3 years of experience working in medical device manufacturing or finish medical device assembly and testing.
Familiar with FDA Quality Systems Regulations and ISO13485 Quality System.
Experience of Windchill and SAP.
Knowledge and methodology of six sigma and Lean manufacturing.
Knowledge of process verification and validation knowledge.
Knowledge of EMC and regulatory test requirement.
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
• Learn more about .
• Discover .
• Learn more about .
If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care .
משרות נוספות שיכולות לעניין אותך

Your Role:
Quality Control and Improvement
- Support MQ and SQE to conduct incoming failure parts analysis.
- Work with quality team to fulfil QMS requirement and support TUV, CFDA, and FDA audit.
Line Sustaining
- Update WI and DHR according to ECR from designer or PPC.
- Daily NC analysis, find root cause and drive improvement.
- Support change controller to execute ECO in production on time and minimize the line
- Introduce new product / new process / new part in production.
LEAN and Cost Reduction
- Continuously improve production efficiency by standardized work, line balance and automation project.
- Optimize production process and eliminate waste using lean method and tools.
- Organize and lead the lean activities and other improvement project.
Equipment Trouble Shooting and Improvement
- Familiar with electrical test platform.
- Identify opportunities to improve current equipment or create new equipment and work with R&D or supplier to realize the requirement.
- Define the URS to guide new equipment purchasing and the equipment qualification.
- Define the gauge calibration requirement.
Digital Transformation and data analysis
You're the right fit if:
B.S. or above in electrical, electronic engineering.
Familiar with AC, DC design and tuning.
Experience of X-Ray testing is preferred.
8 years of experience working in medical device manufacturing or finish medical device assembly or testing.
Familiar with FDA Quality Systems Regulations and ISO13485 Quality System.
Experience of Windchill and SAP.
Knowledge and methodology of six sigma and Lean manufacturing.
Knowledge of process verification and validation knowledge.
Knowledge of EMC and regulatory test requirement.
How we work together
• Learn more about .
• Discover .
• Learn more about .

You're the right fit if:

The Software Development Engineer is responsible for collaborating with the team to establish software quality goals and development practices, fostering continuous improvement and excellence in software development through stringent standards and methodologies. The role develops software to log and store performance data, usage, errors, etc., enabling continuous monitoring of solutions and products for improved reliability and performance. The role integrates software components and third-party libraries into existing systems, ensuring smooth functionality and interoperability with minimal disruption. The role analyzes and optimizes application performance, identifying and resolving bottlenecks to enhance user experience and system efficiency, ensuring software meets performance benchmarks. The role suggests improvements to existing workflows, demonstrating good understanding of user/ product requirements in the areas of responsibility and mentors team members, motivating and unifying team.
1. Design and Development of Clinical Application Software
Develop software for advanced clinical applications in CT image processing, such as:
Quantitative imaging (e.g., stroke, organ segmentation).
Post-processing tools (e.g., multi-planar reconstruction, 3D visualization).
Disease detection and characterization (e.g. contrast analysis, plaque analysis, tissue differentiation).
Partner with clinical and R&D teams to understand end-user requirements and translate them into development tasks.
Focus on creating intuitive, efficient, and user-friendly interfaces and workflows for clinical users.
2. Image Processing Algorithm Development and Integration
Implement, optimize, and integrate medical image processing algorithms, such as:
Iterative reconstruction techniques.
Noise reduction, contrast enhancement, and artifact correction.
AI-based image analysis models (e.g., segmentation, classification, pattern recognition).
Collaborate with data scientists and algorithm engineers to integrate proprietary algorithms into clinical applications.
3. Clinical Workflow Optimization
Analyze clinical workflows and recommend software features to streamline processes for radiologists, technicians, and physicians.
Ensure the software can adapt to real-world clinical scenarios and meet the operational needs of hospitals and imaging centers.
4. Performance Optimization
Ensure high-performance software for real-time CT image processing.
Optimize GPU/CPU utilization for computationally heavy algorithms, such as 3D visualization and iterative reconstructions.
Conduct profiling and benchmarking for resource-intensive tasks to ensure efficiency and scalability.
5. Regulatory Compliance and Documentation
Develop medical imaging software in compliance with industry standards and regulations, including:
IEC 62304 (Software Life Cycle for Medical Devices).
ISO 14971 (Risk Management for Medical Devices).
DICOM (Digital Imaging and Communications in Medicine) standards.
Maintain proper documentation, including software design descriptions, user manuals, and testing logs.
Support software verification and validation (V&V) to ensure regulatory compliance.
6. Clinical Testing and Validation
Build test cases and use real clinical datasets to validate the accuracy, usability, and robustness of image processing applications.
Conduct usability testing and interviews with clinicians and radiologists to identify pain points and areas for improvement.
Assess image quality and algorithm performance on a wide variety of datasets to ensure reliability and accuracy in clinical applications.
7. Cross-FunctionCollaboration
Work closely with radiologists, clinical application specialists, software testers, and regulatory teams to ensure clinical and regulatory objectives are met.
Assist sales and marketing teams by providing clinical insights and supporting customer-facing documentation.
8. Research and Innovation
Stay up-to-date with trends and innovations in CT imaging, medical image processing, and related AI/ML techniques.
Explore and propose new software features or solutions to enhance clinical outcomes and diagnostic capabilities.
REQUIREMENTS
The position requires the following personal capabilities and competence for acceptable performance:
1. Educational Background
Bachelor’s or Master’s degree in Computer Science, Biomedical Engineering, Software Engineering, Medical Physics, or a related field.
Preferred: Advanced degree (Master’s/PhD) in related fields, especially with a focus on medical image processing.
Core Programming Skills
Proficiency in programming languages such as C#, C++ , Python , or Java .
Experience with parallel computing and GPU acceleration frameworks (e.g., CUDA , OpenCL , or OpenMP ) for optimizing medical image processing tasks.
Image Processing Expertise
Strong understanding of CT imaging principles and reconstruction techniques (e.g., FBP, iterative reconstruction, spectral imaging, photon-counting CT).
Experience in medical image processing with toolslike ITK, VTK,or OpenCV.
Familiarity with advanced imaging techniques, such as noise reduction,multi-energy/spectralCT processing, volumetric CT image analysis, and 3D rendering.
Algorithm Development and Optimization
Experience with developing and integrating AI/ML models, such as computer vision techniques (e.g., segmentation, detection, classification).
Knowledge of libraries or frameworks like TensorFlow or PyTorch for developing AI-driven clinical applications.
System and Performance Optimization
Experience in software optimization for high-volume data processing and real-world clinical applications.
Knowledge of multi-threaded programming and memory management for improving algorithm performance.
Data Standards and Medical Systems
Strong understanding of DICOM standards and PACS/HIS/RIS integration.
Ability to design software that seamlessly integrates into healthcare workflows and conforms to interoperability standards.

You are a good fit if:

Senior Electrical Engineer (STET)
1. Early engagement in advanced development focusing on supplier innovation, technical support and supplier part industrialization.
2. Improve product quality, optimize design, integrate supply chain and reduce raw material cost for mass production products.
3. Co-work with cross functions team (RD, Supplier Chain, Quality Dept.) and different modality to improve product system performance, Integrate and optimize supply chain.
4. Product life cycle management.
5. Review and ensure adequacy of supplier part qualification activities.
You're the right fit if:
1. Bachelor/master’s degree (Electrical Engineering, Automatics Engineering, Information Engineering,or relatedengineering discipline), CET-4 or above.
2. 10+ years electrical design or related experience.
3. Experience within a regulated industry is plus, medical devices desirable.
4. Solid understanding of design for manufacturability process, electrical system design and test set up, risk estimate and mitigation plan.
5. Familiar with electrical components selection, analysis and design, good experience of schematic and layout design, verification, and failure root cause analysis.
6. Excellent communication skills and self-confident manner at work.
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
• Learn more about .
• Discover .
• Learn more about .
If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care .

Your role:
You're the right fit if:
How we work together
This is an office role.
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.
The pay range for this position in (Stamford, CT) is $135,000 to $216,000
US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.

Your role:
Quality Control and Improvement:
- Support MQ and SQE to conduct incoming failure parts analysis.
- Work with quality team to fulfil QMS requirement and support TUV, CFDA, and FDA audit.
Line Sustaining:
- Update WI and DHR according to ECR from designer or PPC.
- Daily NC analysis, find root cause and drive improvement.
- Support change controller to execute ECO in production on time and minimize the line interruption.
- Introduce new product / new process / new part in production.
LEAN and Cost Reduction:
- Continuously improve production efficiency by standardized work, line balance and automation project.
- Optimize production process and eliminate waste using lean method and tools.
- Organize and lead the lean activities and other improvement project.
Equipment Trouble Shooting and Improvement:
- Familiar with electrical test platform.
- Identify opportunities to improve current equipment or create new equipment and work with R&D or supplier to realize the requirement.
- Define the URS to guide new equipment purchasing and the equipment qualification.
- Define the gauge calibration requirement.
You're the right fit if:
B.S. or above in electrical, electronic engineering.
Familiar with AC, DC design and tuning.
Experience of X-ray testing is preferred.
3 years of experience working in medical device manufacturing or finish medical device assembly and testing.
Familiar with FDA Quality Systems Regulations and ISO13485 Quality System.
Experience of Windchill and SAP.
Knowledge and methodology of six sigma and Lean manufacturing.
Knowledge of process verification and validation knowledge.
Knowledge of EMC and regulatory test requirement.
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
• Learn more about .
• Discover .
• Learn more about .
If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care .
משרות נוספות שיכולות לעניין אותך