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Quality Assurance Manager
full-timeShanghai

Summary

Location

Shanghai

Type

full-time

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About this role

Job Title

Quality Assurance Manager

Job Description

Job Responsibilities:
• Facilitates operations performance monitoring, reporting, improvement and development, facilitates improvement programs in factory, and supports analytical testing and Supplier Quality Engineering (SQE), Supplier Quality Assurance (SQA) and Purchasing.
• Conducts assessment of impact to Process Failure Mode and Effects Analysis (PFMEA) and associated controls in relation to design changes and assists in Manufacturing Process Development and Design Transfer activities.
• Leads analysis of defects for determining dispositions of non-conformances, drives management of Non-Conformances (NC) and Quality Notifications (QN) and facilitates implementation of effective Corrective and Preventive Actions (CAPA) actions.
• Handles non conformance events and investigations in the factory and guides material review board activities for non-conformance disposition management.
• Facilitates timely quality engineering and quality assurance tasks, ensures manufacturing quality systems are maintained, handles single or complex process validation and process improvement activities, and helps in completion of New Product Introduction (NPI) and product transfers in factory.
• Possesses working knowledge of generic products/services and Quality Engineering and Continuous Improvement techniques, follows processes and operational policies in selecting methods for obtaining solutions, and frequently interacts with supervisors and functional peer groups to gain cooperation of others.
• Acts as an advisor to subordinates to meet schedules and/or solve technical problems, develops and administers schedules and performance requirements, and may have budget responsibilities.
• Cultivates effective relationships, demonstrating full understanding of area of specialization, demonstrates good working relationships with suppliers, and previous experience of participation in several New Product Introductions (NPIs).
• Leads validation protocols, facilitates production builds to support validation activities, analyzes data for reports, process improvement initiatives, and validation activities.
• Utilizes advanced statistical analysis methods to interpret complex data trends, resolve a wide range of moderate complexity requests, and provide strategic insights for continuous enhancement of quality standards and process efficiency.
• Discusses detailed, strategic quality metrics and reports with stakeholders, highlighting significant achievements, emerging trends, and actionable insights to drive advanced improvement initiatives and ensure regulatory compliance.
• Delivers specialized advanced training programs on cutting-edge quality standards, advanced methodologies, and best practices, fostering alignment across functions and advancing excellence in operational practices at an expert proficiency level.
• Cultivates effective relationships with internal/external partners and provides influence over projects and peer groups, demonstrating full understanding of area of specialization.

Minimum required Education:
Bachelor's / Master's Degree in Mechanical Engineering, Electronics Engineering, Science or equivalent.

Minimum required Experience:
Minimum 2 years of experience with Bachelor's in areas such as Quality Engineering, Safety Engineering, Process Engineering or equivalent OR no prior experience required with Master's Degree.

Preferred Skills:
• Process Quality Management
• Data Analysis & Interpretation
• Design for Quality (DFQ)
• Root Cause Analysis (RCA)
• CAPA Methodologies
• Regulatory Requirements
• Manufacturing Processes
• Process Monitoring
• Privacy, Safety and Security Risk Assessment
• Technical Documentation
• Process Engineering
• Continuous Improvement


How we work together
We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week.
Onsite roles require full-time presence in the company’s facilities.
Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.
Indicate if this role is an office/field/onsite role.
About Philips
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 our business.
• Discover our rich and exciting history.
• Learn more about our purpose.
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 here.

Other facts

Tech stack
Operations Performance Monitoring,Supplier Quality Engineering,Supplier Quality Assurance,Process Failure Mode and Effects Analysis,Non-Conformances Management,Corrective and Preventive Actions,Process Validation,New Product Introduction,Statistical Analysis,Quality Metrics Reporting,Advanced Training Delivery,Process Improvement,Quality Engineering,Continuous Improvement,Material Review Board,Design Transfer

About Philips

Over the past decade we have transformed into a focused leader in health technology.

At Philips, our purpose is to improve people’s health and well-being through meaningful innovation. We aim to improve 2.5 billion lives per year by 2030, including 400 million in underserved communities.

We see healthcare as a connected whole. Helping people to live healthily and prevent disease. Giving clinicians the tools they need to make a precision diagnosis and deliver personalized treatment. Aiding the patient's recovery at home in the community. All supported by a seamless flow of data.

As a technology company, we – and our brand licensees – innovate for people with one consistent belief: there’s always a way to make life better.

Visit our website: http://www.philips.com/
Follow our social media house rules https://www.philips.com/a-w/about-philips/social-media.html

Team size: 10,001+ employees
LinkedIn: Visit
Industry: Hospitals and Health Care

What you'll do

  • This role involves facilitating operations performance monitoring, improvement programs, and supporting supplier quality activities, while also leading the analysis of defects and driving the management of non-conformances and CAPA implementation. The manager will guide material review board activities, ensure manufacturing quality systems are maintained, and handle process validation and improvement tasks related to NPI and product transfers.

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Frequently Asked Questions

What does a Quality Assurance Manager do at Philips?

As a Quality Assurance Manager at Philips, you will: this role involves facilitating operations performance monitoring, improvement programs, and supporting supplier quality activities, while also leading the analysis of defects and driving the management of non-conformances and CAPA implementation. The manager will guide material review board activities, ensure manufacturing quality systems are maintained, and handle process validation and improvement tasks related to NPI and product transfers..

Why join Philips as a Quality Assurance Manager?

Philips is a leading Hospitals and Health Care company.

Is the Quality Assurance Manager position at Philips remote?

The Quality Assurance Manager position at Philips is based in Shanghai, China. Contact the company through Clera for specific work arrangement details.

How do I apply for the Quality Assurance Manager position at Philips?

You can apply for the Quality Assurance Manager position at Philips directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about Philips on their website.