דרושים Rf Coil Engineer ב-Philips ב-סין

Job Responsibilities:
• Participates in full software development processes, working with broader autonomy and in pairing mode with other software team members, challenging requirements, design, and quality.
• Own defibrillator application module development. Like network, alarm, audio, GUI, and data acquisition, etc. Deliver high-quality software solutions that meet software requirements.

• Own design document. Deliver high-quality technical documents, including UML diagrams, detailed design, API specification, and user guidance.

• Participate in BSP development.

• Conducts thorough code reviews to ensure adherence to coding standards, identify potential bugs, and promote best practices in software development, fostering a culture of continuous improvement and high-quality code.
• Develops and executes comprehensive test plans, including unit, integration, and system tests, to ensure software reliability, performance, and adherence to specifications.
• Diagnoses and resolves software defects by analyzing logs, reproducing issues, and implementing effective fixes to enhance software reliability and performance.Bachelor's Degree in Computer Science, Software Engineering, Information Technology OR Vocational Education in Information Technology or equivalent.No prior experience required with Bachelor's Degree OR minimum 4 years of experience with Vocational Education in areas such as Software Development, Software Design and Architecture, Testing and Quality Assurance or equivalent.
Preferred Skills:
• Linux C/C++ 11

• Unit test Framework, like gtest, cxxtest.
• FEMA

• SysML/UML Design

• Github/Gitlab
• Agile Methodology(DevOps)
• Software Development Life Cycle (IEC62304)
• Medical industry
• Software configuration management

• uboot

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 .

Your role:

Lead T&V work packages

Development of reproducible and maintainable test methods (mechanical and electronical test methods for elements, (sub)system integration, functional and non- functional tests) corresponding to design input specifications

(in considerations of costs, timing, quality,efficiency)

Tests and measurements coordination, execution, and reporting

Conducting feasibility studies on new marketing claims related to product performance and end user benefits

Analyzing and post-processing of measurement data by using statistical techniques

MSA/ test method validation

Carrying out testing and providing Technicaldocumentation in compliance with internal procedures andregulations/standards

Supporting/ leadingproblem solving activities in order todefinedetermineroot cause of the problem

Contributingto functional continuous improvement plan and knowledge base

To succeed in this role, you should have the following skills and experience

Technical background, preferablydegree inmechanical or electricalmechanicalor electengineering, mechatronics, physics or comparable subject

8+ years of experience in R&D area or manufacturing researchlaboratory(electronicalengineering, test development, manufacturingquality assuranceor research) including solid understanding of test method development and skillful in test execution

Understanding of MSA methodology/ test method validation, statistical techniques

Veryood communication skills (veral and writtenEnglish and Chinese) and social skills since you will be working collaboratingwith colleaguesof many disciplines

Ability to work in group – flexibility in order to work with and provide support for number of people

Practical, with a strong hands-on mentality, also able to manage and delegate tasks when necessary

Experience in creating high quality technical documentation

Good understanding of development process and testing of consumer products

Strong analytical skills (detail data analysis, effective research, creative thinking and efficient problem solving)

Advantages

Six SigmaExperience in creating high quality technical documentation

Strong analytical skills (data analysis, effective research, creative thinking and efficient problem solving)

Knowledge of scripting languages (Excel,Matlab, Python) and Knowledge of connectivity and sensor technologies is an advantage

nderstanding of development process

Ability to work in group – flexibility in order to work with and provide support for number of people

Practical, with a strong hands-on mentality, also able to manage and delegate tasks when necessary

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 .

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

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• Discover .

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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.

Key Responsibilities:

Participate in the supplier sourcing process, evaluating potential new suppliers for quality engineering capabilities.

Perform quality engineering capability assessments of potential new suppliers.

Develop, execute, monitor, and control APQP plans as part of the NPI process.

Contribute to the Supplier Project Book content, ensuring detailed documentation.

Ensure critical-to-quality characteristics are effectively communicated and implemented by suppliers.

Manage Part Submission Warrant plans, deliverables, line release, and completion.

Drive supplier quality improvement and development through the APQP process.

Analyze defects to determine if they are supplier-related and initiate notifications if necessary.

Handle Supplier Quality Notifications (SQNs) and Supplier Corrective Action Requests (SCARs).

Drive APQP plan development, execution, monitoring, and control as part of sustaining changes.

Execute supplier performance monitoring, reporting, improvement, and development activities.

Conduct supplier quality risk assessment and mitigation activities.

Assess and coordinate Supplier Change Requests.

Develop supplier competence where needed, fostering continuous improvement.

You're the right fit if:

Bachelor’s degree in Engineering, Quality Management, or a related field.

A minimum ofyears of experience in supplier quality engineering, preferably with a focus on medical products.

Strong knowledge of ISO 13485 standards.

Knowledge of Statistical methods and analysis. Experience with Quality tools (MSA, Process Capability and SPC).

Know well and experienced

Excellent analytical and problem-solving skills.

Ability to travel as needed for supplier assessments and quality audits.

Preferred Qualifications:

Experience in personal health, medial

Certified Quality Engineer (CQE) or other relevant certifications.

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 .

In this role, you have the opportunity to

• Work as a member of the Transducer Product Industrialization Engineering Team supporting both the introduction of exciting, new, state-of-the-art Ultrasound transducer products and providing feedback to the product design team in the area of design for testability (DfT).
• ISC Product Industrialization Engineer is responsible for engineering tasks associated with manufacturing test development. regulatory compliance, design transfer, qualifications, and introduction of products and their associated manufacturing test processes to meet cost and quality goals

You are responsible for (but not limited to)

• Being an integral part of shaping the dynamics between the Test and R&D teams ensuring a collaborative team effort leading to on-time deployments
• Developing new cost effective test strategies through partnering with other team members, Philips R&D specialists and third parties
• Maintaining regulatory compliance according to Philips Healthcare quality system
• Test solution maintenance, upgrade and creation per test requirements from product design team.

You are part of

The fast-paced environment that places emphasis on a first time right approach, as such in-depth knowledge of product design, test solution design and regulatory compliance is expected.

To succeed in this role, you should have the following skills and experience

• B.Sc. or M.Sc. in Electrical Engineering or similar discipline
• Proficient English communication skills – incl. but not limited to good verbal, written and presenting skills.
• Min 5 years’ experience developing test and measurement systems using modular instrumentation or similar is a must
• A proven track record in working with cross-functional development teams to ensure timely and effective deployment of test solutions is a must
• Experience with the design, use or test of printed circuit board preferred
• Experience in medical device or other regulated industries preferred
• Firmware programming capability preferred.

The successful candidate must be able to demonstrate aptitude for:

• Digital design requiring signal processing and transformation
• Analog design requiring a frequency domain DC to at least 50 MHz

Onsite roles require full-time presence in the company’s facilities.Indicate if this role is an office/field/onsite role.
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