דרושים Supplier Account Manager ב-Philips ב-China, Shenzhen

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;

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.

Your Role

As the Senior Procurement Project Manager, you will drive end-to-end sourcing initiatives for electrical component modules, focusing on pre-NPI (New Product Introduction) phases. You’ll act as the strategic interface between engineering/module teams and our commodity teams, translating product and technical requirements into actionable sourcing briefs and enabling supplier-driven innovation.

Key Responsibilities

• Cost Optimization Leadership: Champion cost optimization by challenging the status quo and finding the right balance between product requirements, consumer needs, and supplier capabilities. Leverage deep insight into electrical components and product functionality to drive competitive advantage.
• Project Leadership: Lead pre-NPI scouting and sourcing projects for electrical components, ensuring alignment with product development timelines and technical specifications.
• Cross-Functional Interface: Serve as the bridge between module teams and procurement, facilitating clear communication and strategic alignment.
• Sourcing Briefs: Translate complex product and engineering requirements into structured, actionable sourcing briefs.
• Innovation Enablement: Identify and pursue supplier-enabled innovation opportunities tied to concrete NPI product needs.
• Roadmap Facilitation: Guide long-term roadmap discussions between module teams and suppliers to ensure future readiness and strategic alignment.
• Negotiation Strategy: Support defining negotiation strategies with our commodity team and support execution to maximize business outcomes.
• Risk & Value Assessment: Evaluate supplier capabilities, risks, and value contributions in the context of product and business goals.
• Lifecycle Support: Oversee sourcing activities across product lifecycle phases, including Phase-In/Phase-Out (PIPO) planning.
• Resilience: Support initiatives through kaizen events and continuous improvement programs to shorten lead times, define global supply footprint and local eco systems.

What You Bring

• Bachelor’s or Master’s in Electrical Engineering or related field.
• 10+ years of experience in procurement or sourcing, with a focus on electrical components.
• Proven success in leading complex sourcing projects and cross-functional collaboration.
• Strong understanding of global and China-specific supply markets and trends.
• Excellent communication, stakeholder engagement, and project management skills.

Preferred Qualifications

• Experience in consumer goods or health technology sectors.
• Experience with digital procurement platforms and analytics tools.
• Experienced with latest LLM and AI tools to leverage in your daily work
• Certifications such as PMP, CPSM, or APICS.
• Multilingual capabilities and international work experience.

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 .

• Leads project-wide verification reviews and optimization efforts to ensure comprehensive coverage of system and sub-system verification, minimizing duplication and increasing transparency, working under limited supervision.
• Develops an expert understanding of designated systems, acting as a subject matter expert for the development team and providing insights on behaviors, implementation, and verification methodologies.
• Implements designs that exceed product specifications, regulatory requirements, and international standards, actively participating in risk management activities to enhance product safety.
• Conducts reviews of prototypes, specifications, and test equipment to evaluate design concepts, fostering a culture of innovation and experimentation.
• Utilizes in-depth knowledge of Geometric Dimensioning and Tolerancing (GD&T) and precise datuming techniques to create and interpret complex engineering drawings, ensuring accurate dimensioning, tolerancing, and tolerancing stack-ups.
• Implements stringent drawing standards, including ISO-A and ISO-E formats, ensuring all engineering documentation incorporates precise datum references.
• Participates in cross-functional reviews, documenting and resolving associated issues, and maintaining effective communication with teams and management.
• Communicates effectively with stakeholders, offering supporting services and collaborating with customers and internal departments to ensure seamless project execution.
• Acts as the primary liaison between stakeholders, development teams, and groups, ensuring clear communication throughout the project lifecycle.
• Ensures strict adherence to company policies, procedures, and quality standards throughout all hardware design and development activities, fostering a culture of consistency, compliance, and continuous improvement.
• Contributes to the development, modification, and execution of organizational policies impacting immediate operations and potentially organization wide.
• Utilizes advanced analytical skills to address high complexity requests efficiently, applies conceptual thinking to develop innovative solutions and strategies.
• Bachelor's / Master's Degree in Electrical Engineering, Electronic Engineering, Mechanical Engineering or equivalent.
• Minimum 5 years of experience with Bachelor's in areas such as System Architecture, System Design, Hardware Engineering or equivalent.

• Strong leadership abilities and experience in managing and developing teams.

• Proven experience in a senior engineering management role within both medical and hand-held electronics products industry.

• Experience in mechanical and embedded systems development.

• In-depth knowledge of industry standards, technological trends, and innovation strategies.

• In-depth knowledge of design for reliability.

• Proficiency in data analytics and metrics-driven decision-making.

• Effective communication skills and ability to influence stakeholders at various levels.

• Strategic thinking and ability to define and drive technological roadmaps.

• Proficiency in written and oral communication in English and Chinese.

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 and Corrective/Preventive Action 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;