דרושים Operational Quality Lead ב-Philips ב-פולין

is responsible for developing and implementing a quality control framework to align with organizational goals and regulatory requirements, ensuring high product quality and compliance. The role leads the Quality Control team, overseeing quality EU-MDR control processes, and conducting root cause analysis to address critical issues. The role coordinates with cross-functional teams, utilizes advanced quality management tools, and reviews documentation. The role manages audits, establishes and monitors performance metrics, ensures equipment accuracy, and drives continuous improvement projects using Lean methodologies.

Your role:

• Implements quality control framework, ensuring alignment with overall organizational goals and regulatory requirements to maintain high standards of product quality and compliance.
• Leads and manages the Quality Control team, guiding and mentoring them, actively contributing to employee selection, performance management, compensation management, career development, and overseeing operational processes.
• Oversees the development, implementation, and maintenance of quality control processes, procedures, and systems to ensure consistent and reliable product quality across all stages of production.
• Oversees thorough root cause analysis and leads problem-solving initiatives for critical quality issues, driving the development and implementation of effective corrective and preventive actions.
• Effectively manages escalations by the right identification of involved stakeholders with keeping E2E accountability of Quality Control Team over the EU-MDR verification process.
• Coordinates with cross-functional teams, including research and development, production, regulatory affairs, and supply chain, to integrate quality control measures into product design, development, and manufacturing processes.
• Reviews and approves comprehensive quality documentation, including inspection records, validation protocols, audit reports, and regulatory submissions, ensuring accuracy and compliance with industry standards.
• Oversees internal and external audits of processes, suppliers, and subcontractors to ensure adherence to quality management systems and regulatory standards, addressing and resolving any non-conformances.
• Establishes and monitors key quality performance metrics and trends, generating strategic insights and presenting to executive leadership to inform decision-making and drive continuous quality improvement initiatives across the organization.
• Ensures the calibration, validation, and maintenance of all quality control equipment and instrumentation, guaranteeing accurate and reliable data for high-precision quality assessments.
• Leads and drives continuous improvement projects within the quality control department, applying Lean methodologies to optimize processes, reduce waste, enhance product quality, and achieve operational excellence.
• Addresses difficult to moderately complex issues or problems, requiring the evaluation of identifiable factors, following established processes and operational policies in selecting methods and techniques for obtaining solutions and possesses working understanding of Corrective and Preventive Action (CAPA), applicable regulations, requirements, and standards.

Requirements:

• Bachelor's / Master’s degree in Industrial Engineering, Manufacturing Engineering or equivalent in Quality or Supply Chain or Finance environment.
• Minimum 4 years of experience in areas such as Quality Control, Quality Assurance, Production, Manufacturing or equivalent.

• Good leadership skills: influencing others, organizational sensitivity;

• Experience in being a trusted advisor to market senior level, demonstrated ability to drive impact;

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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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 .

Your role:

• Capability Leadership
  • Define a strategic plan by identifying opportunities and capabilities that are highly relevant and can create value for businesses and customers
  • Champion the adoption of modern technologies that can significantly improve Quality, Productivity & Experiences

• People & Culture
  • Define and execute on a strategic workforce plan and competence development plan
  • Establish and grow a world-class team of engineers and architects focused on modular, secure, and sustainable software design. Develop capabilities that are seen as distinctly differentiating for the businesses.
  • Inspire and lead a cross-functional team with empathy, accountability, and a growth mindset
  • Foster a culture of innovation, continuous learning, and psychological safety.
  • Mentor team members and support career development aligned with organizational goals.

• Stakeholder Engagement
  • Collaborate closely with internal business units, product teams, and clinical stakeholders to align technology with healthcare outcomes
  • Build strong relationships with external partners, industry forums, and technology vendors to stay ahead of the curve.

• Execution Excellence
  • Drive talent onboarding, engagement and career growth. Ensure execution is efficient, compliant to processes and QMSes and meets the program commitments (time, quality, costs)
  • Ensure compliance with healthcare regulations, data privacy, and security standards.
  • Measure and communicate the impact of modernization efforts on business and patient outcomes

You're the right fit if:

• Bachelor’s Degree inInformation Technologyor related field. Master's degree is preferred.
• Minimum of 18 years of progressive experience in the development and release of Products and Solutions, especially in a regulated environment like healthcare is strongly preferred
• Proven experience in a leadership role, engaging and building competent engineering teams.
• Strong software engineering background with prior hands-on experience in software development.
• Excellent communication and interpersonal skills to collaborate effectively across teams and with stakeholders.
• Strong understanding of building solutions leveraging GenAI and non-GenAI, familiarity with major cloud platforms (e.g., Azure, AWS, GCP) and their AI/ML services deployment, monitoring, and MLOps principles.
• Familiarity with major cloud platforms (e.g., Azure, AWS, GCP) and their AI/ML services

How we work together

Onsite roles require full-time presence in the company’s facilities.

This role is an office-based 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 culture of impact with care .

The Service Parts Quality Engineer is primarily responsible for supporting the establishment of a compliant and effective Quality Management System (QMS) for Circular Lifecycle Solutions.

The role participates in developing and revising QMS process documents, such as SOPs and quality manuals, ensuring their accuracy and currency. This includes document control and training administration related activities, continuous improvement projects to create processes and standard ways of working to support a smoothly functioning QMS. This role will also include

quality engineering responsibilities such as root cause analysis, CAPA support, APQP, Quality rep on project teams, etc.

Your role:

• Ensure compliance with the Quality Management System, in accordance with Philips Policies and applicable worldwide regulations and standards

• Execute procedures for nonconformance(s) – CAPAs, SCARs, and Audit Corrective Actions including monitoring effectiveness

• Support and Review where applicable Process Development, Validation, and Quality Controls throughout the lifecycle of supply chain products/solutions ensuring all necessary documents/records are maintained throughout the lifecycle of the product/solution

• Partner with Supplier Quality on processes related to the approval and acquisition of purchased services, solutions, materials, components, sub-assemblies, and completed products and to ensure vendor assessments are completed

You're the right fit if:

• You have a min. Bachelor's Degree in Mechanical Engineering, Industrial Engineering, Electronics Engineering, Science or equivalent

• You have 4+ years of experience in Quality Engineering, Safety Engineering, Process Engineering area

• You have experience in Quality Management Systems, Quality Audits or equivalent in highly regulatedenvironments/industriessuch as MD, Pharma, Automotive

• You understand regulatory requirements

• You have expertise in quality management systems (QMS)

• You are skilled in troubleshooting

• You are experienced in KPI monitoring and reporting

• You are adept at data analysis and interpretation

• You drive process improvements

• You are familiar with agile methodology

• You provide effective user training and support

• You develop training content

• You possess strong business acumen

• You are fluent in English

Our benefits

• Hybrid model of working

• Annual bonus based on performance achieved

• Private medical care with the option to extend it to family members

• Benefit System cards

• Discount for Philips’ products

• Wide variety of trainings & learning opportunities

• Promotion of a healthy lifestyle in the office

• Employee Assistance Program

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 Service Parts Quality Engineer is primarily responsible for supporting the establishment of a compliant and effective Quality Management System (QMS) for Circular Lifecycle Solutions.

The role participates in developing and revising QMS process documents, such as SOPs and quality manuals, ensuring their accuracy and currency. This includes document control and training administration related activities, continuous improvement projects to create processes and standard ways of working to support a smoothly functioning QMS. This role will also include

quality engineering responsibilities such as root cause analysis, CAPA support, APQP, Quality rep on project teams, etc.

Your role:

• Ensure compliance with the Quality Management System, in accordance with Philips Policies and applicable worldwide regulations and standards

• Execute procedures for nonconformance(s) – CAPAs, SCARs, and Audit Corrective Actions including monitoring effectiveness

• Support and Review where applicable Process Development, Validation, and Quality Controls throughout the lifecycle of supply chain products/solutions ensuring all necessary documents/records are maintained throughout the lifecycle of the product/solution

• Partner with Supplier Quality on processes related to the approval and acquisition of purchased services, solutions, materials, components, sub-assemblies, and completed products and to ensure vendor assessments are completed

You're the right fit if:

• You have a min. Bachelor's Degree in Mechanical Engineering, Industrial Engineering, Electronics Engineering, Science or equivalent

• You have 4+ years of experience in Quality Engineering, Safety Engineering, Process Engineering area

• You have experience in Quality Management Systems, Quality Audits or equivalent in highly regulatedenvironments/industriessuch as MD, Pharma, Automotive

• You understand regulatory requirements

• You have expertise in quality management systems (QMS)

• You are skilled in troubleshooting

• You are experienced in KPI monitoring and reporting

• You are adept at data analysis and interpretation

• You drive process improvements

• You are familiar with agile methodology

• You provide effective user training and support

• You develop training content

• You possess strong business acumen

• You are fluent in English

Our benefits

• Hybrid model of working

• Annual bonus based on performance achieved

• Private medical care with the option to extend it to family members

• Benefit System cards

• Discount for Philips’ products

• Wide variety of trainings & learning opportunities

• Promotion of a healthy lifestyle in the office

• Employee Assistance Program

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 .

Your role:

• Leadership & Strategy Execution: Lead and drive continuous improvement programs across cross-functional, global, and regional domains that align with Philips' overarching strategy and business objectives.

• Quality Improvement Initiatives: Act as a change agent to support data-driven quality improvements, enhancing operational quality performance to meet internal and external customer needs.

• Process Compliance: Spearhead quality investigations and support improvement projects that reduce complexity and bolster process compliance, ensuring delivery of the Quality strategy.

• Data Utilization: Analyze operational data to identify quality issues, trends, and hotspots, facilitating targeted improvements for operational effectiveness and efficiency.

• Procedure Development: Develop and refine procedures, ensuring team-wide compliance and understanding of regulatory requirements.

• Quality Process Execution: Support the effective management and execution of quality processes across regions, particularly in handling suspected non-conforming products.

You're the right fit if:

• Root Cause Investigations: Proficient in CAPA, 8D, 6 Sigma methodologies.

• Data Analysis: Expertise in identifying improvement opportunities through comprehensive data analysis.

• Change Management: Strong skills in leading change and program management.

• Process Orientation: Experience in process mapping, value stream mapping (VSM), and other process-oriented methodologies.

• Improvement Focus: Passionate about driving improvements and ensuring excellence in quality processes.

Qualifications:

• University degree

• Experience in a problem solving, improvement implementation, change management and quality preferably within a global organization.

• Proven track record in leading successful improvement projects.

• Strong analytical and problem-solving skills.

• Excellent communication and senior stakeholder management abilities.

Our benefits:

• Annual bonus based on performance achieved

• Private medical care with the option to extend it to family members

• Benefit System cards

• Discount for Philips’ products

• Wide variety of training & learning opportunities

• Promotion of a healthy lifestyle in the office

• Employee Assistance Program

Indicate if this role is an office.
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 .

Quality Group Circular Lifetime Solutions (CLS) oversees the Quality Assurance in the processes related to the supply and distribution (forward and reverse) of service parts, refurbished systems (CE), repair, services and their supply chain, including compliance with regulatory requirements and procedures for regulated products/businesses. We lead and coordinate the Quality support within the scope of service parts and repair to ensure successful and compliant processes with service parts, refurbished systems and repair business partners.

The role is about to assure that Quality systems of suppliers and Philips Health Systems meet Purchasing Controls and regulatory requirements.

Your role:

• Support the quality teams to ensure adequate plans are in place for spare parts supply, and repair service providers, refurbished systems and 3rd party related activities

• Collaborate with Supply Chain leaders to ensure all quality related processes and support where necessary to ensure successful supplier base to the regions

• Monitor operational compliance of supply chain and repair for service and parts, reporting on a regular base and escalate in case compliance issues

• Leads assigned areas in support of Products Transfers – process validations – planning

• Supports assigned areas in service transfers

• Supports the development and execution of operations quality disciplines such as Validations, Process Controls, Inspection Plans, Control Plans

• Ensure raw materials/components/products and services are released from suppliers to Philips according to the agreed requirements.

• Drive quality, compliance and continuous improvement at suppliers

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You're the right fit if:

• You have a Bachelor Degree in relevant technical function

• You have a relevant experience in root cause analysis, corrective and preventive action methods

• You are experienced in Product/process development and/or supplier quality improvement

• You have knowledge about problem solving with quality tools such as: 6-sigma / 8-D / CAPA / FMEA/ 5WHY etc.

• Exposure to production/quality development and control methods; CtQ definition, DfSS, SPC, APQP, FMEA, Control Plans, etc.

• You have an auditing skill sets

• You have an ability to write procedures and technical documentations

• You have an excellent MS office skills

• You are self-starter, curious

• You are fluent in English

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Your role:

• Verify supplier documentation to ensure compliance with medical regulations.

• Assist with data extraction & analysis in Excel.

• Review and interpret documents and email correspondence for accuracy.

• Work within SAP and other internal systems to manage documentation.

You’re the right fit if:

• You are a student in at least 2nd year of Bachelor studies.

• You are detail-oriented with strong analytical abilities.

• You are proficient in using MS Office package, especially Microsoft Excel.

• You are a quick learner with the ability to recognize patterns and adapt to new tasks.

• You are fluent in English and Polish.

• You are available to work at least 25 hours/week

What We Offer:

• A 6-month internship based on a civil contract with competitive salary.

• Flexible working hours that can be adapted to your university schedule.

• The opportunity to use English in your daily activities.

• Access to learning platforms like LinkedIn Learning and Philips University.

• A chance to build your career within an international company known for innovation.

• Discount for the multisport card.

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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