

Job Description
This involves being a confident advisor on quality and reliability engineering topics.
You are responsible for
Ensure that appropriate project plan and quality plans are made that include all stages of the product’s lifecycle, targets and strategy for a robust software products development.
Validates key design inputs including requirements, specifications, useability, reliability, performance, supportability, manufacturability, localizability, safety, security, privacy serviceability, sustainability, and costs.
Provides effective oversight during the execution of the Quality Plan and any risk management activities, and of all design related activities during the lifecycle.
Contribute during design and development to identify critical quality attributes (CTQ, CTS) and ensure that appropriate mitigations and design controls are applied to mitigate the risks.
Facilitate design failure mode and effect analysis to identify failure modes early in the design and development process and apply design, manufacturing and inspections to mitigate the risks.
Ensure with objective V&V evidences that design output meets the design input.
Leading quality related problem solving with the cross functional teams
Using post-market data for analytics and statistics to report on the product’s performance in the market (provide feedback to manufacturing, suppliers, or design teams) and initiate field actions when required.
Act as a single point of contact (person assigned to) for project team(s); you’re responsible to ensure the product’s design quality relatedrequirements/criteriaare complete and meet the quality standards for every project milestone.
Make substantial contribution to integrate reliability engineering activities with the medical device development activities.
Effective oversight of project deliverables and provide quality input, including safety, efficacy, regulatory. Facilitate the product defect investigations and actions during defect management review meetings.
Participate in audits and regulatory inspection as design quality SME and guide other cross-functional stakeholders on technical aspects and audit conduct.
To succeed in this role, you should have the following skills and experience
Specific skill requirements for this role include:
Bachelor’s engineering degree with 12 years / Master’s degree with 10+ years of experience; in Software Engineering , quality engineering, SW Quality- or Reliability Engineering role in the medical or aerospace industry.
Software testing experience will be an added advantage
Ability to define detailed software quality and reliability plans for new medical product developments to ensure those are safe, effective and reliable.
Ability to contribute to Risk Management and lead FMEA activities for new products and assurance that control measures are translated in appropriate (critical) requirements.
Strong exposure to application of Design Controls; ability to do thorough Design Reviews during new product development to ensure robust designs that further improve patient safety and product quality.
Ability to partner with V&V teams to assure thorough Verification, Validation and Useability testing.
Analyze development and field data for Product Safety, Quality and Reliability performances and areas for further improvements of Product design and related development processes.
Well conversant with statistical data analysis, regressionmodeling,reliability growth assessment and other quality techniques
Experience with adequate and accurate review of DHF and DMR documents.
Understanding of global medical device regulations, requirements, and standards, such as 21CFR820, ISO13485, EU MDR, IEC 62366, IEC 62304 and ISO 14971.
Experience with working in multidisciplinary teams in a high-tech R&D environment.
Effective interpersonal, written and oral communication skills expected.
Ability and willingness to work onsite
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Our hybrid working model is defined in 3 ways:
משרות נוספות שיכולות לעניין אותך

Sr. Software Technologist I - Full Stack Development EngineerYour role:
• Acts as a technical coach for a team or domain, being recognized and approached by team members for expertise and guidance, ensures consistent application of best practices and high standards across projects.
• Integrates software components and third-party libraries into existing systems, ensuring seamless functionality and interoperability with minimal disruption.
• Conducts and participates in code reviews, providing constructive feedback to peers and ensuring adherence to coding standards and best practices to maintain code quality.
• Analyzes and optimizes application performance, identifying and resolving bottlenecks to enhance user experience and system efficiency, ensuring the software meets performance benchmarks.
• Stays current with emerging technologies and industry trends, incorporating new tools and methodologies to improve development processes and product quality.
• Develops software to log and store performance data, usage, errors, etc., enabling continuous monitoring of solutions and products for improved reliability and performance.
• Collaborates with cross-functional teams, including product managers, designers, and QA engineers, to define, design, and ship new features, ensuring alignment with project goals and user needs.
• Resolves a wide range of moderate complexity requests in creative ways, demonstrating good judgment in selecting methods and techniques for obtaining solutions.
You're the right fit if:
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 .

Job Title :
In this role, you have the opportunity to
Ensures that appropriate SW Quality plans are made that include all stages of the software life cycle and supports SW Quality Plan design
Validates key design inputs like: usability, reliability, performance,
supportability,
serviceability,sustainability and costs
Provides effective oversight of: the execution of the SW Quality Plan and any Risk Management activities, and of all design related activities during the software lifecycle
You are responsible for
To lead quality related problem solving for software
Use post-market analytics and statistics to report on software performance in the field (provide feedback to manufacturing, suppliers or design teams) and
initiate field actions when required
Act as a single point of contact (person assigned to project team) responsible
to ensure that software design quality relatedrequirements/criteriaare completed and meet SW Quality standards for every PRP milestone
Make a substantial contribution to ways of combining Agile withmedical softwaredevelopment
To succeed in this role, you should have the following skills and experience
Working knowledge of appropriate global medical device regulations, requirements and standards. consumer product regulations, industry. standards, such as 21 CFR Parts 803, 806 and 820
8-10 years of work experience in a related field
Experience in IEC 62304 and software quality experience mandatory
• Learn more about .
• Discover .
• Learn more about .
Our hybrid working model is defined in 3 ways:

Job Responsibilities:
Onsite roles require full-time presence in the company’s facilities.Indicate if this role is an office/field/onsite role.
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• Discover .
• Learn more about .

- Design, develop, and operate internal Code Hub Platform Engineering services on top of our AWS/GitHub/Artifactory foundational layer.
- Implement infrastructure-as-code and automation pipelines using Terraform, GitHub Actions, and other DevOps tools.
- Lead or co-lead improvements in scalability, reliability, and developer experience for mission-critical services.
- Monitor and continuously improve service performance, cost-efficiency, observability, and compliance with SRE best practices.- Contribute to and support the Backstage Developer Portal as a gateway to platform capabilities and self-service workflows.
Bachelor's / Master's Degree in Computer Science, Software Engineering, Information Technology or equivalent.
- 10+ years of hands-on software engineering experience with proficiency in at least one modern language (e.g., TypeScript, Python, Java, or C#).
- Experience with cloud-native development and deployment, especially on AWS (e.g., ECS, Lambda, S3, CloudWatch).
- Experience designing, securing, and scaling CI/CD pipelines using GitHub, GitHub Actions, and infrastructure-as-code tools.
Master's Degree in Computer Science, Information Technology or equivalent
- Comfortable working with container-based systems (e.g., Docker, Kubernetes) and modern observability tooling.
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 .

Job title:
Cloud Engineer
Your role:
Complexities of the job:
You're the right fit if:
Onsite roles require full-time presence in the company’s facilities.
Indicate if this role is an office/field/onsite role.• Learn more about .
• Discover .
• Learn more about .

Your role:
You're the right fit if:
A minimum of 5 years of experience successfully developing complex medical devices (hardware, software, consumables) Products for acute/emergency care/hospital markets are necessary.
How we work together
This role is an office-based role.
• Learn more about .
• Discover .
• Learn more about .

Job Description
This involves being a confident advisor on quality and reliability engineering topics.
You are responsible for
Ensure that appropriate project plan and quality plans are made that include all stages of the product’s lifecycle, targets and strategy for a robust software products development.
Validates key design inputs including requirements, specifications, useability, reliability, performance, supportability, manufacturability, localizability, safety, security, privacy serviceability, sustainability, and costs.
Provides effective oversight during the execution of the Quality Plan and any risk management activities, and of all design related activities during the lifecycle.
Contribute during design and development to identify critical quality attributes (CTQ, CTS) and ensure that appropriate mitigations and design controls are applied to mitigate the risks.
Facilitate design failure mode and effect analysis to identify failure modes early in the design and development process and apply design, manufacturing and inspections to mitigate the risks.
Ensure with objective V&V evidences that design output meets the design input.
Leading quality related problem solving with the cross functional teams
Using post-market data for analytics and statistics to report on the product’s performance in the market (provide feedback to manufacturing, suppliers, or design teams) and initiate field actions when required.
Act as a single point of contact (person assigned to) for project team(s); you’re responsible to ensure the product’s design quality relatedrequirements/criteriaare complete and meet the quality standards for every project milestone.
Make substantial contribution to integrate reliability engineering activities with the medical device development activities.
Effective oversight of project deliverables and provide quality input, including safety, efficacy, regulatory. Facilitate the product defect investigations and actions during defect management review meetings.
Participate in audits and regulatory inspection as design quality SME and guide other cross-functional stakeholders on technical aspects and audit conduct.
To succeed in this role, you should have the following skills and experience
Specific skill requirements for this role include:
Bachelor’s engineering degree with 12 years / Master’s degree with 10+ years of experience; in Software Engineering , quality engineering, SW Quality- or Reliability Engineering role in the medical or aerospace industry.
Software testing experience will be an added advantage
Ability to define detailed software quality and reliability plans for new medical product developments to ensure those are safe, effective and reliable.
Ability to contribute to Risk Management and lead FMEA activities for new products and assurance that control measures are translated in appropriate (critical) requirements.
Strong exposure to application of Design Controls; ability to do thorough Design Reviews during new product development to ensure robust designs that further improve patient safety and product quality.
Ability to partner with V&V teams to assure thorough Verification, Validation and Useability testing.
Analyze development and field data for Product Safety, Quality and Reliability performances and areas for further improvements of Product design and related development processes.
Well conversant with statistical data analysis, regressionmodeling,reliability growth assessment and other quality techniques
Experience with adequate and accurate review of DHF and DMR documents.
Understanding of global medical device regulations, requirements, and standards, such as 21CFR820, ISO13485, EU MDR, IEC 62366, IEC 62304 and ISO 14971.
Experience with working in multidisciplinary teams in a high-tech R&D environment.
Effective interpersonal, written and oral communication skills expected.
Ability and willingness to work onsite
• Learn more about .
• Discover .
• Learn more about .
Our hybrid working model is defined in 3 ways:
משרות נוספות שיכולות לעניין אותך