דרושים Product Quality Engineer ב-Philips ב-Israel, Haifa

As Manufacturing SW Development- you will support Haifa site Operations Activities to enable Software applications, equipment and infrastructures readiness for smooth functionality enabling operation with compliance and quality.
Your role:

• Develop software in accordance with development standards and procedures.
• Integrate your developments into the product and maintain them.
• Maintain sustainable approach for Data integrity in ISC application across BU
• Design a technical solution that meets the functional requirements.
• Works with stakeholders to develop the architectural runway in support of new business features and capabilities.
• Participate in the technical choices in accordance with the architecture choices established by the project managers.
• Create and maintain the CI/CD pipelines necessary for the deployment of our solution
• Accountable for Data accuracy in ISC application across BU to ensure E2E data flow
• Collaborate with cross geographical, cross functional teams and stakeholders at multiple levels to obtain alignment and ensure successful solution implementation.

You're the right fit if you have:

• Relevant academic degree as Industrial Engineering, Software engineer or equivalent significant experience.
• 5+ years of software development experience
• hands on experience of C# .Net, .NET Core, JavaScript, CSS, and HTML.
• Experience with SQL database developments
• Industry 4.0 knowledge involving cloud environment experience.
• Azure services such as Databricks, Data factory, Data Lake, IoT Hub and Streaming Analytics. – an advantage
• Experience with IoT technologies, including OPC UA and edge devices. – an advantage
• Production processes knowledge and understanding – an advantage.
• Healthy technology curiosity with fast learning ability

• Mastery of Git and CI/CD Tools like Azure DevOps – an advantage 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.
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  • 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 commitment to diversity and inclusion .

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Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.
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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• Discover .
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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 an Operations Quality Team Manager, you will lead Q&R activities in the system plant as a PQE team manager. You will be responsible for driving product quality improvements by leveraging statistics and data analysis techniques to enhance processes. Your role will involve close collaboration with production, manufacturing engineering, and suppliers to ensure process control, quality assurance, effective failure analysis, and continuous improvement.

Your role:

• Provide clear vision and strategy for the PQE team, ensuring alignment with organizational quality goals.
• Build and develop the capabilities of the quality team, fostering a culture of continuous improvement and collaboration.
• Lead MRB activities, periodic quality reviews, and provide actionable insights.
• Lead “real-time” manufacturing line investigations, identify root causes of issues, and ensure the implementation of corrective actions through comprehensive reporting and follow-up.
• Implement and monitor production and process controls, including Process Validation (PV), Equipment Qualification (EQ), Control Plans, and pFMEA.
• Maintain compliance with ISO 13485, FDA regulations, and other relevant standards.
• Prepare for and support external audits (regulatory, customer) and perform internal pre-audits.
• Act as a liaison between R&D and Operations to ensure a smooth transition during NPI and change management And work closely with Production, Supply Chain, and Manufacturing Engineering to improve overall quality performance.

You're the right fit if you have:

• Bachelor's degree in engineering, production technology, science, quality assurance, mechanical engineering, or other related field.
• A minimum of 3 years of experience as a quality manager or in a similar role.
• A minimum of 5 years of experience as a product quality engineer
• In-depth knowledge of quality assurance methodologies, standards, and regulatory requirements (e.g., ISO 13485, FDA, MDR).
• Fluent in English, both written and verbal.

s

• Experience working in medical device, pharmaceutical
• Proficiency in statistical analysis tools (e.g., Minitab, JMP) and methods such as Six Sigma.
• Expertise in quality systems, CAPA management, and risk assessment.
• Familiarity with SAP or other ERP systems for quality tracking.
• Experience in NPI (New Product Introduction) and production readiness activities.
• Knowledge of advanced manufacturing processes, automation, and Industry 4.0 principles.

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.
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 commitment to diversity and inclusion .

Your role:

AI ecosystem offering 30+ contracted AI Vendors and 90+ AI solutions available.

Key responsibilities:

• Evaluate (new) Supply Chain concepts and designs for new or existing value streams, in line with Business strategy. Scope is upstream as well as downstream Supply Chain
• Analyze new scenarios and quantify the performance with end-to-end scope for management decisions working closely together with adjacent functions
• Contribute to the deployment of strategic, tactical, financial and operational plans by driving continuous improvement in supply chain performance through Supply Chain analysis and process improvements.
• Organize & develop analytics towards the defined Supply Chain metrics
• Initiates, coordinates and integrates improvements through projects of Supply Chain process optimization and organizational change within field of expertise
• Provide specialist support for supply chain issues, e.g.: Assist, support and provide backup coverage for Supply Chain team member to execute SC activities such as stock take, physical inventory count, inventory accuracy in allocation and consumption, material demand, sales order entry, and purchase order entry.
• Work closely with IT experts to clarify requirements and approve solutions designs by IT.
• 3
  rd
  party SW vendor management

• Interface with 3rd party SW vendors for SW deliveries and project management
• Monitor and establish subscription and royalties way of work and reporting

You're the right fit if:

• Customer first attitude
• 3-5 years in various functions of the Supply Chain
• Project management skills
• Basic knowledge on IT landscape
• Accurate, analytical and process driven way of working, able to keep the integral overview.
• Results oriented: take personal accountability to deliver results.
• Quality first mindset.
• Has in depth knowledge of the functional area, the operational logistic processes and the business strategies.

Indicate if this role is an office/field/onsite role.
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 .

Manufacturing Process engineer
Your role:

As Manufacturing Engineer, you are responsible for the end-to- end manufacturing processes of CT detectors in the clean room environment, maintaining efficiency, reducing costs, improving sustainability, and maximizing profitability through tools and equipment of the manufacturing systems, leading to predictable, reliable, stable and efficient production processes.

In this position, you will play a crucial role in Haifa’s detection center, overseeing both established and new assembly processes and driving initiatives for manufacturing process optimization

Responsibilities:

• Monitoring both automated and manual assembly processes in clean room environment
• Support line-downs and troubleshoot problems associated with manufacturing processes
• Initiating and overseeing process technology development activities
• Accountable for process and manufacturing requirements based on Product Specifications
• Provides active inputs on improving the manufacturability of new products at the release stage.
• Identifying, designing, implementing and validating manufacturing processes, tools and equipment enabling quality and efficiency.
• Preparation & Release of Work instruction, PFMEA, Process validation docs etc.
• Executing processes with compliance to safety, regulatory- and environmental requirements as well as local laws, Philips General Business principles and other policies.

Education/Skills and Experience Requirements:

• BSc. or master’s degree in mechanical/Mechatronics/Material/Chemical/Biochemical Engineering
• 3+ years’ experience in similar role as process engineer
• Experience in problem solving and root cause analysis: Fishbone 8D, 4M methods
• Familiarity with statistical analysis and DOE (JMP, Minitab, proficiency in Excel)
• Excellent technical skills and knowledge of process-related standards
• Experience in Quality Management Systems (preferably in the medical industry), SAP, Windchill
• Preferably experience with process validation (PMAP, pFMEA, IQ, OQ, PQ)
• Continuous improvement mindset, result driven with quality approach
• Strong personal & communication skills in English

Indicate if this role is an office/field/onsite role.
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 .

The Quality Analyst is responsible for driving and supporting CT/AMI Sites compliance via development and implementation of IT tools to efficiently operate and maintain the QMS.

Your role:

• Development and implementation of IT tools transformation projects to efficiently operate and maintain the QMS and provide training on key compliance topics.
• Provide compliance and other support as needed.

You're the right fit if:

• Student of Science or equivalent in technical/ engineering
• Knowledge and development skills in various Microsoft tools, including Power Automate, Microsoft Graph, Power BI, Share Point, Website, etc.
• Fluent verbal and written English
• At least 3 semesters of studies remaining till graduation and availability for at least two working days per week
• Good communication skills and convinced team player
• Attention to detail and self-directed

Preferred

• Familiar with medical device regulations and standards (such as, US FDA QSR, EU MDD, Canadian CMDCAS, Japan PAL regulation and other WW regulations and standards) – an advantage
• Prior experience in a Medical Device company in a Quality Engineering role – an advantage

Indicate if this role is an office/field/onsite role.
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 .

Thedrives product quality improvement activities, using statistics and to improve processes. works with production, manufacturing engineering and suppliers in the areas of process control, quality control and assurance, data collection, failure analysis, corrective actions, reporting for early detection and correction and continuous improvement. Responsible for “real time” investigation of failures, finding root causes, issuing summarizing report and following-up corrective actions implementation.
Your role:

• Manages and follows-up quality activities.

• Participate and lead “real time” manufacturing line investigations to identify cause and containment actions. Work with Production, Supply and Manufacturing Engineer personnel.

• Interpret manufacturing outputs and customer inputs, define problems, collect data, establish facts, and draw valid conclusions.

• Select and apply quality procedures and methods, appropriate inspection strategy and statistical techniques.

• Establish and monitor quality/process control for high risk parts and high risk suppliers.

• Create and administer an effective closed-loop corrective action program.

• An active member on the production release of new products, responsible for quality plan preparation.

• Plan and participate in internal manufacturing audits and assessments as a co-auditor.

• Participate in the Material Review Board process to dispose off rejected material..

You're the right fit if you have:

• Practical Engineering / BA / BSc degree.

• 2-4 years of work experience in a manufacturing plant.

• Good understanding of statistical methods, quality tools and methodologies (i.e. 8D, DMAIC, SPC, FMEA, Control Plan, LEAN).

• Fluent English

This role is an office role.
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 .