דרושים Senior Innovation Marketing Manager ב-Philips ב-China, Shenzhen

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.
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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 .

As a Clinical Application Specialist IGT-S Indonesia, you will provide clinical expertise through pre-sales presentations, product demonstrations, application training and handing over of company products. You will assist the sales staff in assessing potential application of company products to meet customer needs and preparing detailed product clinical specifications for the development and implementation of customerapplications/solutions.

Your Role:

• Supporting Account Managers by providing clinical decision support for products and solutions, including sales presentations, product demonstrations. Support and advise the sales force during customer acquisition.
• Developing and executing winning clinical sales strategies to expand market share
• Actively participating with sales team in coordinating and executing clinical evaluations, product demonstrations and presentations
• Educating sales team on emerging clinical issues and positioning solutions to address these market changes. Keep up to date with new developments in the clinical application and operating field of the relevant equipment
• Supporting new products launches
• Customer Trainings and handover of newly installed IGT-S products or new end-users.
• Set up application training schedules, in close cooperation with the customer.
• Train customers in applying the best possible clinical procedures and protocols to achieve optimal usage of the deliveredcathlabs,patient monitors and C-arm equipment.
• Report to IGT-S business unit on difficulties in optimal usage of the equipment
• Responsible for delivering customized (competency based) training material pack – if / when required
• Support user group meetings if / when required.
• Conduct regular visits to customers to obtain direct feedback from them about the quality of the training delivery and the customer satisfaction.
• Support and advise the sales force during acquisition.
• Stay "on track" with the new developments in the clinical application and operating field of the relevant equipment.
• Be aware and to always manage the safety standards required by the company, including radiation protection, health and safety regulations. In the event of hazards or accidents, to take immediate control of the situation and involve the safety advisor from the regional office.
• Ensure that all clinical applications training, with both new and existing customers, complies with the company's quality policy.
• Responsible for reporting customer feedback according to applicable quality standard policy and follow up relevant assigned quality & regulatory training in a timely manner.
• As a Clinical Application Specialist IGT-S Indonesia, you will be part of APAC IGT-S Clinical Applications Specialist Team and you may need to cover other countries outside of Indonesia in case other IGT-s clinical application specialist are not available.

You are the right fit if:

• University degree in relevant allied health discipline majors
• Cathlab, C-arm and radiation safety in-depth knowledge, proficiency in one of the clinical segments such as Interventional Cardiology,Radiology, vascular,Neurology.
• Preferably minimum of 2-5 years of experience at Clinical applications or as a radiographer in a hospital setting.
• Experience on using Cathlab or C-arms and advanced applications.
• Strong communication and presentation skills.
• Ability to utilize problem-solving, critical thinking and priority-setting skills.
• Speaking, understanding, and writing fluently English in addition to local language.
• Teaching experience in a clinical environment preferred.
• No obstacle to travel extensively with-in Indonesia and within APAC when necessary.

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mid-October to start of November

at least 5 months (preferred 6 months)

Weekly presence:32-40 hours

Your role:

• Supporting the leadership team in the decision-making process by conducting insight generating analysis

• Being responsible for a dedicated departmental support process

• Supporting the day-to-day activities of the GSO which are ever-changing as a result of a dynamic environment and continuous improvement ambition.

You're the right fit if:

• Students who are currently studying towards their Master of science WO (Msc.) in Finance, Economics, Business Administration, Business Management or a related field

• Strong skills and an open and global oriented work mentality

• Advanced knowledge of MS Office (Word, Excel, and PowerPoint)

• Excellent communication and interpersonal skills to interact with senior-level management, previous internship experience in an international organization is an advantage

• Excellent English language skills (written and spoken)

In return, we offer you

Unique working experience at a global HealthTech leading firm. You will have the first insights into the world of Philips and how PIA supports Philips to realize its strategy. In addition, you will be developing hard and soft skills such as communication, analytical and stakeholder management skills.

How we work together

Onsite roles require full-time presence in the companys facilities.

or suppliers

If you

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 .