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We're looking for a Design Verification Team Lead - a design verification technical lead that is responsible for complex SoC sub-system, with cutting edge technology for Nitro system SoC, the foundation of AWS's virtualization, networking, and storage offload infrastructure.

It starts at product definition - we engage from day one, shaping requirements and translating product intent into verification strategies before a single line of RTL is written

It extends into software - we work side-by-side with SW teams, verifying hardware-software interfaces and ensuring seamless integration across the stack, with particular emphasis on networking workloads such as ENA and EFA

It reaches into physical design - we verify physical design aspects within functional verification, bridging the gap between logical correctness and silicon reality

It closes the loop - from spec to silicon, our verification touches every team and every stage of chip development

Key job responsibilities

- Develop and execute verification plans for IO sub-systems - covering interconnect protocols, peripheral interfaces, and system-level integration with a strong connection to networking flows (ENA/EFA).

- Verify IO sub-system features, including interconnect protocols and various accelerator engines.

- Develop and debug C embedded SW as part of hardware-software integration verification.

- Build and maintain UVM-based verification environments for various clusters and sub-systems.

- Verify ARM advanced interconnect protocols (AMBA CHI/ACE/AXI) ensuring correct coherency transactions, performance verification, and protocol compliance.

- Verify the IO virtualization SMMU/TLB operations, page table walks, translation granules, and memory attributes (cache-ability, share-ability).

- Develop constrained-random and directed test strategies targeting corner cases in IO protocol hazards, coherency races, and system boundary conditions.

- Drive coverage closure using functional coverage models, assertion-based verification, and formal methods where applicable.

- Contribute to performance verification - ensuring micro-architectural implementations meet performance targets alongside correctness.

We are looking for talented engineers to join the Pre-silicon Verification team and help us technically lead the challenges of the next decade, developing a semiconductor platform based on revolutionary architecture, and taking part in the development of cutting-edge products within a disruptive system architecture.
Youll have the opportunity to work on the technologies that power the worlds largest cloud provider, in a dynamic, open, and fast-paced environment.

As a software developer in this role, you will have the opportunity to design and deliver the development of engaging features for millions of customers. You will be an integral part of a passionate and creative team that encourages experimentation and innovation on behalf of our customers. You will tackle challenging, novel situations every day and have the opportunity to work with multiple technical teams at Amazon. Along the way, youll learn a lot, have fun and make a positive impact on millions of people.

We are looking for a talented Software Development Engineer with a strong technical background, customer obsession and bias for action with a track record of leading and delivering robust solutions quickly. Strong judgment and communication skills, long-term technical vision, and continuous focus on engineering and operational excellence are essential for success in this role. You will be expected to take ownership, be proficient technically, mentor and grow junior developers, encourage software development best practices, and iterate quickly.

Key job responsibilities
- Design, build, test, and operate features for the Interests experience across web and mobile surfaces.
- Deliver end-to-end solutions with focus on maintainability, performance, and reliability.
- Collaborate with Product and Science to define experiences, run experiments, and iterate based on data.
- Understand latest trends in mobile technology and work across Amazon mobile teams.
- Build AI-powered experiences including personalized updates, relevance explanations, and contextual recommendations.
- Implement analytics events and experiment configurations to measure engagement and retention.
- Relish the idea of solving problems and be comfortable with a degree of ambiguity thats higher than most projects.

In this role, you will join a world-class team of engineers within the Surgical Operating unit responsible for developing medical devices that focus on lung cancer diagnosis.
Our Surgical Operating Unit is one new, powerful operating unit bringing together the people and product portfolio of Surgical Robotics and Surgical Innovations. With our Mission as our North Star, we will build on our legacy of proven surgical solutions and advance the promise of robotics and digital solutions to benefit our customers and patients.
Make your impact by exploring a career with the worlds leading Medical Device company, striving to alleviate pain, restore health, and extend life.

We are seeking a highly qualified and detail-oriented Software Verification Engineer to join our software verification team. This position involves verification and integration of complex, multidisciplinary medical systems. The role requires direct collaboration with cross-functional teams, including software, algorithm, and hardware engineering, to ensure the system meets all functional and performance requirements.

Responsibilities may include the following and other duties may be assigned:
Designing and executing SW verification activities: Proactively identify gaps in performance, accuracy, and quality across the software and algorithmic components of the system. Develop and prioritize test strategies based on risk, impact, and business needs. Create comprehensive test plans to validate functionality, accuracy, and performance.
Automation and continuous improvement: Contribute to the development and expansion of automated testing solutions. Continuously look for ways to improve test efficiency, coverage, and reliability by adopting new tools, scripting approaches, and creative testing methods.
Performing script-based testing: Develop and maintain test scripts to automate and enhance testing processes using Python, MATLAB, or other tools.
Collaborating with cross-functional teams: Work closely with cross-functional teams, including software, algorithm, hardware engineering, quality, and regulatory, to ensure successful testing outcomes.

In this role, you will join a world-class team of engineers within the Surgical Operating unit responsible for developing medical devices that focus on lung cancer diagnosis.
Our Surgical Operating Unit is one new, powerful operating unit bringing together the people and product portfolio of Surgical Robotics and Surgical Innovations. With the Mission as our North Star, we will build on our legacy of proven surgical solutions and advance the promise of robotics and digital solutions to benefit our customers and patients.
Make your impact by exploring a career with the worlds leading Medical Device company, striving to alleviate pain, restore health, and extend life.

We are seeking a highly qualified and detail-oriented Software Verification Engineer to join our software verification team. This position involves verification and integration of complex, multidisciplinary medical systems. The role requires direct collaboration with cross-functional teams, including software, algorithm, and hardware engineering, to ensure the system meets all functional and performance requirements.
Responsibilities may include the following and other duties may be assigned:
Technical leadership: Serve as a technical leader within the verification team, providing guidance, reviewing test approaches and deliverables, and mentoring less-experienced engineers.
Independence: Demonstrated ability to independently lead complex verification initiatives, make sound technical decisions, and drive issues to resolution.
Designing and executing SW testing strategies: Proactively identify gaps in performance, accuracy, and quality across the software and algorithmic components of the system. Develop and prioritize test strategies based on risk, impact, and business needs. Create comprehensive test plans to validate functionality, accuracy, and performance.
Continuous improvement of testing processes: Identify process improvement opportunities by implementing new tools and optimizing methods.
Performing script-based testing: Develop and maintain test scripts to automate and enhance testing processes using Python, MATLAB, or other tools.
Collaborating with cross-functional teams: Work closely with cross-functional teams, including software, algorithm, hardware engineering, quality, and regulatory, to ensure successful testing outcomes.

As a Quality Program Manager, you will play a critical role in the integration of CathWorks quality systems and processes into our global quality framework. Based in Kfar Saba, this onsite position is responsible for ensuring the seamless alignment of design controls, CAPA, complaints handling, software development lifecycle, and regulatory compliance processes. Working across multiple functions, you will help drive quality excellence, regulatory readiness, risk mitigation, and process harmonization while supporting the successful integration of innovative digital health technologies into the portfolio.
Responsibilities may include the following and other duties may be assigned:

Work with the Integration Lead on integration planning for quality systems, processes, and documentation, ensuring alignment with our QMS, regulatory requirements, and integration objectives.
Lead the mapping, migration, and harmonization of CathWorks quality processes, including document control, training, audits, CAPA, complaints handling, and design control activities, ensuring compliance with FDA, MDR, ISO, and our standards.
Oversee CAPA and complaints management processes, including root cause analysis, corrective and preventive actions, regulatory reporting, and continuous process monitoring.
Provide oversight of software development lifecycle processes, including requirements management, design reviews, validation, testing, and software design controls in regulated environments.
Ensure all quality activities comply with applicable regulatory requirements (FDA, MDR, ISO 13485, 21 CFR Part 11, etc.), including electronic records and signatures, risk management, audit readiness, and support for internal and external audits.
Facilitate communication, training, and stakeholder engagement across CathWorks and Medtronic, identify process gaps, drive continuous improvement initiatives, and monitor integration progress through metrics and regular reporting.

As a Quality Engineer based in Kfar Saba, you will play a key role in supporting day-to-day quality activities while helping harmonize quality and regulatory processes across the organization. This position focuses on design controls, CAPA, complaint handling, software development lifecycle activities, and regulatory compliance within a regulated medical device environment. You will collaborate with cross-functional teams to ensure quality system requirements are effectively implemented, maintained, and continuously improved, supporting the delivery of innovative technologies that advance patient care.

Responsibilities may include the following and other duties may be assigned:
Assist in aligning and implementing design control processes, including requirements management, design reviews, verification/validation, and traceability.
Support the mapping, migration, and harmonization of quality system processes, including document control, training, audits, and related quality activities; support internal and external audits as applicable.
Participate in the integration and standardization of CAPA and complaints handling processes, ensuring effective root cause analysis, corrective and preventive actions.
Support software development lifecycle processes, including requirements management, design reviews, validation, and testing.
Ensure all integrated processes meet applicable regulatory requirements (FDA, MDR, ISO 13485, 21 CFR Part 11, etc.), including electronic records and signatures, risk analysis, and audit readiness.
Assist in updating and maintaining quality documentation, provide training to stakeholders on new or revised processes, identify process gaps, and support continuous improvement initiatives.

we are a fast-growing global medical device company that develops and manufactures innovative drug-delivery and infusion solutions across the continuum of care, from hospital to home. We are looking for an experienced V&V Manager to lead our V&V function and team within the R&D
Job Description
* Lead the V&V function and define the verification and validation strategy for new products and design changes.
* Manage, develop, and provide technical leadership to a multidisciplinary team of V&V engineers, including goal setting, workload allocation, mentoring, and performance development.
* Ensure complete, risk-based TEST coverage and traceability from product and system requirements through TEST evidence and final reports.
* Review and approve V&V plans, protocols, reports, deviations, and supporting technical documentation.
* Oversee system -level hardware, software, mechanical, and disposable-set testing in the R&D laboratory and at external laboratories and subcontractors.
* Lead experimental design, data analysis, structured problem-solving, and root-cause investigations.
* Plan resources, equipment, schedules, and priorities, and monitor execution against project milestones and quality objectives.
* Partner with Systems, R&D, Quality, Regulatory, Clinical, and Project Management teams, and provide V&V support during audits and regulatory submissions. Reports to: R&D Director

We are looking for a Verification Engineer who embodies ambition and positivity, who can passionately take ownership of their responsibilities, collaborating effectively with remote teams to not only meet but exceed our objectives and fulfil the evolving needs of our expanding customer base.
The Verification engineer we look for will be a highly talented and motivated person, who is a real team player and can collaborate closely with engineers from other disciplines and physicists.
Responsibilities:
Practicing the full range of verification aspects
Creating a verification environment from scratch (drivers, monitors, coverage...)
VIP (DDR/PCIe/AXI) integration
Defining verification sequences via a complex control-flow constraint set
System understanding of a full-stack product with strong HW-SW coupling
Reference model integration
Test plan definition
Defining verification flows and creating the proper infrastructure to support it

We are looking for a Verification Engineer who embodies ambition and positivity, who can passionately take ownership of their responsibilities, collaborating effectively with remote teams to not only meet but exceed our objectives and fulfil the evolving needs of our expanding customer base.
The Verification engineer we look for will be a highly talented and motivated person, who is a real team player and can collaborate closely with engineers from other disciplines and quantum physicists.
Responsibilities:
Practicing the full range of verification aspects
Creating a verification environment from scratch (drivers, monitors, coverage...)
VIP (DDR/PCIe/AXI) integration
Defining verification sequences via a complex control-flow constraint set
System understanding of a full-stack product with strong HW-SW coupling
Reference model integration
Test plan definition
Defining verification flows and creating the proper infrastructure to support it

Required QC Engineer
Department: Physics & metallurgy
Reports to: VP Physics & metallurgy
The Ceramic QC Lab role is responsible for operating a quality assurance lab based on existing testing systems and developing new testing methodologies. This role requires learning and applying QC testing methods, working independently to solve ceramic-related problems, maintaining attention to detail, and finding methodologies for conducting various tests.
Responsibilities:
Conduct QA Tests on Raw Materials: Perform QA tests on incoming raw materials and during their storage period, especially for materials with long storage times.
Monitor Ceramic Quality: Conduct QC tests to monitor ceramic quality throughout preparation, mixing, and printing stages.
Data Reporting: Input results to engineers at workstations and maintain direct communication to ensure consistency between measurement results and observed results in the field.
Improve Testing Methodologies: Continuously learn and enhance testing methods to refine results, ensuring up-to-date status analysis that matches results from different workstations.
Develop and Operate Monitoring Systems: Establish and operate a monitoring system for ceramic quality, accounting for calendar, process changes, equipment changes, and quality correlations between raw materials and batch variations.
Receive guidance from the Chemistry and Process teams to support QC methods.
Create Efficient QC Systems: Develop additional methods for an efficient QC system that provides an up-to-date quality status for ceramics, enabling troubleshooting without halting the process or workstations (e.g., material correction, refreshing, and adjusting working conditions to align material quality with the process).