Philips Quality Project Lead 

China, Guangdong Province, Bao'an District 

109299877

Quality Project Lead

In this role, you have the opportunity to

• Be accountable for oversight of system and hardware quality and risk management throughout the product life cycle.
• Provide independent oversight of the design input process, design Verification & Validation activities, design transfer and product realization, and performance in the field to ensure that all design requirements are effectively met.
• Provide analytics to the Business on the efficacy and efficiency of the design and product realization processes

You are responsible for

• Ensure that appropriate quality plans are made that include all stages of the life cycle of the product and supports Quality Plan design
• Validate key design inputs like usability, reliability, performance, supportability, manufacturability, localizability, safety, security, privacy, serviceability, sustainability and costs
• Provide effective oversight of the execution of the Quality Plan, any Risk Management activities, and of all design related activities during the product/system lifecycle
• Lead the project team to work out the control point from FMEA through control plan.
• Performs independent technical assessment on product quality performance and post-market product quality analysis
• Can Lead quality related problem solving and root cause analysis, risk assessment, during design and manufacturing
• Use post-market analytics and statistics to report on product quality performance in the field (provide feedback to manufacturing, suppliers or design teams) and initiates field actions when required
• Contact Window to handle customer and market quality issue compliant and feedback
• Being an ‘ambassador’ for quality assurance and drive quality awareness and improvement in project teams.
• Compliance, effectiveness and efficiency of the developed product.
• Act as a single point of contact (person assigned to project team) responsible to ensure that hardware design meets quality and compliance standards for every milestone

You are a part of

• A professional site production & development quality team with international exposure.

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

• Education: Bachelor’s degree or above.
• Mechanical Engineering Background preferable in Medical Device type products
• High Degree of experience working with Global Quality and Regulatory requirements with high dependencies of documented processes and deliverables
• Experience: More than 3 years of experience in product quality testing and approbation field.
• Competencies and skills:
  • Problems solving Familiar with analytical tools, such as FMEA, process control plan
  • Solid knowledge/experience in SPC, G&RR & Process Capability Analysis
  • Working knowledge of appropriate global regulations and standards in areas of consumer goods (e.g. Oral Health Care, Consumer Electrical Goods, Medical Device)
  • ISO9001 & ISO13485
  • Black Belt preferable Green belt minimum.
• Experience of working in Global Matrix organization
• High morale with excellent work ethic, integrity and attitude.
• Teamwork orientated, Self-motivated & able to Work Independently
• Good quality engineering related tools knowledge and implementation skills.
• Good team work spirit and communication skills.
• Good skills of project management.
• Very good English and Chinese both verbal and written skill.

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