Job Title

Job Description

Location: Shanghai Zhangjiang

In this role, you have the opportunity to

• Responsible for quality operations at Philips Shanghai including but not limited to receiving and final inspection teams, compliance, quality engineering, and leading and developing quality team.
• This position requires a seasoned quality professional from medical devices industry with a proven track record in change management and people development. 

You are responsible for

• Supervise quality team supporting the manufacturing and warehousing facility, including but not limited to acceptance activities, manufacturing, labeling and packaging.
• Provide direction and partner with cross functional team in root cause analysis and issue resolution related to manufacturing, quality management systems, and compliance. 
• Serve as the subject matter expert for sites’s quality metrics (nonconformances, CAPAs, training, etc), operating procedures, and work instructions for internal discussions and internal and external audits.
• Optimize procedures and work instructions a part of continuous improvements to the quality management system.
• As needed, review and approve procedures, work instruction, protocols, reports for the manufacturing site, including but not limited to process validation and equipment qualifications. 
• Partner with manufacturing and supply chain in product quality improvements, including but not limited to product yield and Cost of Non-Quality measures.
• Oversee tracking and trending of the site’s quality performance data and provide direction on issue resolution for negative trends and results. 
• Partner with Business and Operation team members in product transfers, new product development and continuous improvement projects
• Establishes and manages the necessary quality programs to ensure the Company meets the Quality System requirements per company procedures and applicable federal regulations and international standards
• Work with cross functional team on operations quality mentorship programs, development and succession planning
• Submit and manager quality budget in accordance with Philips requirements

You are a part of

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

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

• Bachelors or Master’s degree required, Engineering or Science preferred
• 8-10 years in FDA regulatory industry required (Medical Devices or Pharmaceutical, or combination thereof)
• 7 years in Quality required; and 6+ years of management level experience required. 
• Must have demonstrated ability to work with senior/executive leaders and be able to engage/influence cross functional leadership teams

In return, we offer you

We offer experiences and opportunities that add many unexpected and enriching moments to our employees’ lives. Especially when the innovative health technologies and solutions they help develop benefit their own friends and family.

Why should you join Philips?

Working at Philips is more than a job. It’s a calling to create a healthier society through meaningful work, focused on improving 3 billion lives a year by delivering innovative solutions across the health continuum. Our people experience a variety of unexpected moments when their lives and careers come together in meaningful ways. Learn more by watching this video.

To find out more about what it’s like working for Philips at a personal level, visit the Working at Philips page on our career website, where you can read stories from our employee blog. Once there, you can also learn about our recruitment process, or find answers to some of the frequently asked questions.