The Production Quality Engineer at Philips in Haifa is responsible for ensuring manufacturing quality systems are maintained and driving continuous improvement. Key responsibilities include conducting PFMEA assessments, leading defect analysis for non-conformances, managing NC and QN, implementing CAPA actions, and facilitating NPI and product transfers. The role requires utilizing advanced statistical analysis, discussing strategic quality metrics, delivering specialized training, and supporting equipment and facility qualification to enhance quality standards and process efficiency.

Must Have

• Conduct assessment of impact to Process Failure Mode and Effects Analysis (PFMEA)
• Lead analysis of defects for determining dispositions of non-conformances
• Drive management of Non-Conformances (NC) and Quality Notifications (QN)
• Facilitate implementation of effective Corrective and Preventive Actions (CAPA)
• Handle non conformance events and investigations in the factory
• Guide material review board activities for non-conformance disposition management
• Ensure manufacturing quality systems are maintained
• Handle process improvement activities
• Help in completion of New Product Introduction (NPI) and product transfers in factory
• Utilize advanced statistical analysis methods to interpret complex data trends
• Discuss detailed, strategic quality metrics and reports with stakeholders
• Deliver specialized advanced training programs on quality standards and methodologies
• Support equipment and facility qualification for the manufacturing line
• Bachelor's / Master's Degree in Industrial Engineering, Bio-Medical Engineering, Science or equivalent
• Minimum 2 years of experience with Bachelor's in Quality Engineering, Safety Engineering, Process Engineering

Job Description

Job description

Job Responsibilities:

• 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 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.

• 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).

• 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.

• Support equipment and facility qualification for the manufacturing line.

Minimum required Education:

Bachelor's / Master's Degree in Industrial Engineering, Bio-Medical 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.

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.

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.

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