Jobs at Philips in China, Shenzhen

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:

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 .

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 .

You are responsible for

• Takes End to End ownership of complex and high impact Emergency Care and Resuscitation programs with high visibility and importance to the business

• Prepares and implements programs in multi-discipline areas (including Quality and Regulatory, R&D, Operations) in accordance with agreed goals on quality, time, cost and staffing.

• Leads all aspects of the Identification, Investigation andCorrective/PreventiveAction implementation of the CAPA process at the site level.

• Able to solve complex problems using various root cause analysis tools, with goal of focusing team on most impactful and important deliverables.

• Navigates through the complexity of programs by coordinating between the sub-projects, multiple sites, and matrix organization.

• Sets project timelines, uses innovative methods to optimize efficiency, and manages risks to achieve project success

• Ensures team is staffed effectively and utilized to the fullest potential to most efficiently complete projects. Coaches team members and provides feedback to appropriate parties.

• Establishes strong operating mechanisms to track progress, identify issues, overcome obstacles, and define recovery plans.

• Provides ongoing status reports to the business leadership team, highlighting opportunities and risk mitigations.

• Works with Quality and Regulatory to ensure the program is fully compliant with the Quality System, FDA design controls, and global regulatory agency requirements.

• Optimizes project efficiency and innovation via collaboration with other ECR program managers within Program Management Office (PMO) and resource managers in other functions

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

The successful candidate will possess the following knowledge, skills education and experience:

• Bachelor’s degree

• 5+ years of product development experience

• 2+ years of Project Management experience

• PMP certification a plus

• Medical product development experience a plus

• Strong communication skills

• Demonstrated leadership skills showing ownership and successful completion of complex projects

• Strong problem-solving and analytical skills

• Ability to manage competing priorities in a fast paced environment

• Language skills: Fluent in English (both writing and verbal) and Fluent in Mandarin;

• Time zone / Can work under high pressure

• Logical thinking and demonstrated competencies on handling multiple tasks;

You are responsible for:

• Assists in the coordination and execution of projects, ensuring adherence to project timelines, objectives, and deliverables, working under general limited supervision and applies awareness of entrepreneurial skills in daily work.
• Supports project managers in the preparation and maintenance of project plans, schedules, and documentation, facilitating smooth project execution.
• Aids in project reporting activities, gathering relevant data, analyzing project metrics, and preparing reports to communicate project status, progress, and key insights.
• Participates in project meetings, workshops, and forums, capturing meeting minutes, action items, and decisions to facilitate collaboration and alignment among project stakeholders and providing PMO updates.
• Collects and organizes project-related information, documents, and resources, ensuring easy accessibility and retrieval for project team members and stakeholders.
• Ensures the accuracy and integrity of project data and records, performing regular audits, checks, and validations to identify and resolve discrepancies or inconsistencies.
• Provides administrative support to PMO director and team members, coordinating tasks such as communication, scheduling, document management, planning, assisting with expense reporting, and other logistical tasks as needed.
  

Qualification Requirements:

• Bachelor's Degree/ Vocational Education in Business Administration, Project Management or equivalent.

Preferred Skills:

• Language skills: Fluent in English (both writing and verbal) and Fluent in Mandarin
• Strong communication
• Ownership and Commitment
• Logical thinking
• multiple tasks handling
• Stakeholder Partnership
• Emotional Intelligence
• Learning Agility
• Servant Leadership
• Administrative Support
• Documentation & Reporting
• Microsoft Office

Your role:

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:

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:

• Facilitates technical capability assessments of potential new suppliers, ensuring they meet the company's quality standards, and contributes to the supplier selection.

• Conducts & reviews DFMAT (Design for Manufacturing and Assembly Technique), SAF (Supplier Approval Form), MSA (Measurement System Analysis), PFMEA (Process Failure Mode and Effects Analysis), Control Plan, SPC (Statistical Process Control), PV&V (Process Validation and Verification), FAI (First Article Inspection), LRA (Logistics Risk Assessment), and SICR (Supplier Initiated Change Request).

• Develops, executes, monitors, and controls APQP (Advanced Product Quality Planning) plans as part of the NPI process to ensure consistent product quality.

• Contributes to the content of the Supplier Project Book, documenting detailed quality requirements and expectations for suppliers.

• Facilitates collaboration between R&D and suppliers in Design for Excellence (DfX) initiatives to enhance product design quality and innovation.

• Focuses that Critical to Quality (CtQ) characteristics are effectively communicated to suppliers and rigorously maintained throughout the production process.

• Coordinates Part Submission Warrant plans, deliverables, line releases, and completion, ensuring all parts meet specified quality standards before approval.

• Executes supplier improvement and development initiatives on APQP(Advanced Product Quality Planning), providing guidance and resources to enhance supplier processes, ensuring they meet the high standards required for production quality and efficiency.

• Assists with the process of making additions, changes, or deletions to the Approved Supplier List, ensuring that only qualified suppliers are retained.

• Supports in end to end performance management of suppliers, conducts detailed analysis of defects to determine if they are supplier-caused, and acts as an independent reviewer for Supplier Corrective Action Requests.

You're the right fit if:

• Bachelor's/ Master's Degree in Engineering Science, Supply Chain Management, Electrical Engineering, Electronic Engineering or equivalent.

• Rich experience with Bachelor's in areas such as Quality Engineering, Safety Engineering, Process Engineering, Continuous Improvement Techniques or equivalent.