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This Product Designer enjoys solving complex problems and wants meaningful ownership. Youll design experiences across our web and mobile products, working closely with product managers, engineers, and our CEO.
Your access to leadership is part of the work. The CEO will look to you for design recommendations, ask questions, and challenge your thinking. Youll need to explain your choices, raise concerns, and suggest a better approach when you see one.
You dont need every answer or years of executive-facing experience. You do need curiosity, sound reasoning, and the willingness to contribute your own perspective-even when the person across the table is the CEO.
Please include your portfolio with your application. Were interested in how you think as well as what you design.
Why this role is exciting
Direct influence: Discuss problems and design decisions with the people shaping the product, including our CEO.
Meaningful ownership: Take individual projects from an initial problem through exploration, design, and implementation.
Interesting complexity: Make technical workflows easier to understand across cameras, locations, filters, onboarding, and other connected parts of the platform.
Visible impact: Work on improvements that change how customers use the product. For example, our bulk camera onboarding flow helped users add multiple cameras in one process.
Room to grow: Learn through close collaboration with Product and Engineering, with support from the CTO on technical questions and broader work processes.
Freedom to explore: Experiment with different approaches, workflows, and AI tools to improve your work.
What youll do
Turn high-level product requests into clear problems, asking questions before jumping into solutions.
Create user flows, wireframes, prototypes, and polished interfaces for web and mobile.
Consider how a change affects the wider product, including related workflows, navigation, and existing patterns.
Gather insight from product managers, engineers, Solutions Engineers, and other colleagues close to customer needs.
Present your recommendations to teammates and leadership, explaining your reasoning and the trade-offs.
Constructively challenge assumptions-including leaderships-when you see a usability issue or a stronger alternative. Bring examples, evidence, or a proposed solution.
Test and refine designs using feedback, usability testing, and product insights.
Collaborate with engineers through handoff and implementation to help ensure the experience works as intended.
Contribute to our design system and maintain consistency across the product.
Balance thoughtful design with timely delivery as priorities evolve.

The Senior Software Engineer, Edge our company's growing engineering organization and help build the software that runs on the core device layer behind our platform. This role sits within a small, highly impactful team responsible for a hybrid edge system that powers core functionality across video, security, networking, storage, and AI deployment in production environments. You'll work on a resource-conscious, distributed device architecture that spans multiple hardware targets and brings together technologies more commonly seen across both embedded and cloud systems. This is a strong fit for an engineer who enjoys meaningful ownership, thrives in a fast-moving startup environment, and is comfortable building reliable software for systems customers depend on every day.
Location & Travel
Hybrid / Onsite Schedule: Based in Caesarea or Ramat Gan with 2 days a week working from home.
Responsibilities
Contributing to the development of our core edge platform, designed to run across diverse hardware environments as part of a hybrid edge-cloud architecture
Developing and integrating video management capabilities, including streaming, recording, and real-time AI processing
Designing and optimizing systems for low-latency, high-performance workloads at the edge
Building secure and efficient communication pipelines between edge devices and cloud systems
Working closely with AI/ML engineers to deploy and optimize models on-device
Participating in code reviews, debugging, and performance tuning across the stack
Collaborating with a talented team of engineers, AI experts, and leadership in a fast-moving environment.

We are seeking a proactive and detail-oriented AI Regulatory Engineer to ensure that AI-based clinical features for ultrasound systems comply with evolving global regulatory requirements-particularly FDA regulations for AI-enabled medical devices.
This role is critical as AI has become a highly regulated domain, requiring specialized regulatory strategies, risk management approaches, and lifecycle governance. The AI Regulatory Engineer will work closely with AI engineering, clinical, quality, product management, and regulatory affairs teams to define and execute the correct AI regulatory and submission strategy across the full product lifecycle.
Job Description
Key Responsibilities
AI Regulatory Strategy & Compliance
Interpret and apply regulatory frameworks and guidance for AI-enabled medical devices, including FDA, EU MDR/IVDR, and global regulations.
Define and drive AI regulatory strategies for clinical ultrasound features, including SaMD and AI-enabled device functions.
Support FDA submission pathways (e.g., 510(k), De Novo, PMA) for AI-based features, including AI-specific regulatory positioning.
Risk Management & Safety for AI
Lead AI-focused risk management activities in accordance with ISO 14971, addressing AI-specific hazards such as bias, robustness, generalization risk, and clinical misuse.
Perform and maintain AI-specific risk analyses (e.g., AI FMEA, algorithm hazard analysis, clinical performance risk).
Ensure traceability between clinical requirements, AI behavior, risk controls, and verification/validation evidence.
Regulatory Documentation & Submissions
Prepare and maintain AI-related regulatory documentation, including:
AI descriptions and intended use statements
Training and validation dataset descriptions
Performance evaluation and clinical evidence summaries
Algorithm change management and lifecycle documentation
Support creation of FDA-ready AI documentation, including transparency, explainability, and human-factors considerations.
AI Lifecycle & Change Management
Define regulatory-compliant processes for AI updates, retraining, and post-market changes, aligned with FDA expectations.
Support implementation of Predetermined Change Control Plans (PCCP) or equivalent AI lifecycle strategies.
Ensure alignment between AI development practices and regulatory expectations for locked vs. adaptive algorithms.
Cross-Functional Collaboration
Collaborate closely with:
AI engineers and data scientists
Clinical and medical affairs teams
Quality, systems, and V&V engineers
Product management and regulatory affairs
Embed regulatory and safety requirements early into AI design, data strategy, and clinical validation plans.
Regulatory Intelligence & Audits
Monitor evolving AI regulations, FDA guidance, standards, and industry best practices.
Communicate regulatory changes and their impact on AI roadmaps and product strategy.
Support internal audits, design reviews, and external regulatory inspections related to AI and clinical safety.
Provide training and guidance on AI regulatory and safety topics to engineering and product teams.

Systems engineering is a cross-functional engineering discipline centered on an approach, mindset, and process. All activities that consider both the business and the technical needs of the customers with the goal of providing a quality product that meets the users needs. The discipline that executes a robust process of design, creation, and optimization of systems, consisting of identification and quantification of system requirements, creation of alternate system design concepts, performance of design trade studies, selection and implementation of the best designs and verification that the design is properly integrated and executed. Process that proceeds from concept to production to operation.
Responsible for departmental operations planning/execution or is focused on execution of professional activities within a technical discipline. Functions with some autonomy but guided by established policies or review of end results.
The job allows modification of procedures and practices covering work as long as the end results meet standards of acceptability (quality, volume, timeliness etc.).
Job Description
Roles and Responsibilities
Conducts component and product integration. All activities that span multiple components and products and are concerned with how to integrate for maximum performance and operability. Manages product and systems requirements, specifications and flow down. Drives validation and verification activities for the overall product/system, including system level testing. Responsible for defining product requirements for the module / component / subcontractors and partners teams. Manages interface between components and execution organizations.
Responsible for driving CTQ / Risk trades within the teams designing the components. Manages the overall product configuration and configuration control system.
Includes direct people management responsibility including staffing and performance development. Utilizes in-depth knowledge of a technical discipline and analytical thinking and technical experience to execute policy/strategy.
Has knowledge of best practices and how own area integrates with others; is aware of the competition and the factors that differentiate them in the market
Uses some judgment and has some ability to propose different solutions outside of set parameters to address more complicated manufacturing processes with technical variety and/or interdependent production cycles. Uses technical experience and analytical thinking. Uses multiple internal and limited external sources outside of own teams to arrive at decisions.
Acts as a resource for colleagues with less experience. May lead small projects with low risks and resource requirements. Explains information; developing skills to bring team members to consensus around topics within field. Conveys performance expectations and may handle sensitive issues.

The Lead Clinical Applications Engineer is a role within R&D, focused primarily on new product introduction and continuous improvement of post-market Nuclear Medicine and/or PET-CT imaging systems and related software. The role provides clinical and application expertise to product and engineering teams, ensuring solutions meet clinical needs, deliver strong image quality and quantification, and perform reliably in real‑world use.
Working closely with R&D, system engineering, product management, service, and field teams and customers, this role translates clinical needs, customer feedback, and usage insights into practical system and software improvements, while supporting resolution of complex clinical and application‑related issues.
Job Description
Lead Clinical Applications Engineer
Key Responsibilities
Serve as a clinical reference for Nuclear Medicine and PET-CT applications and workflows within R&D programs.
Support investigation of selected complex customer or field issues, translating findings into actionable inputs for product improvement.
Interface with product, software, algorithms, system engineering, hardware, UX, service, and field organizations as needed.
Translate clinical use cases and user needs into system and software requirements in collaboration with engineering teams.
Support design and validation of Nuclear Medicine and PET-CT applications, reconstruction methods, and workflow solutions.
Provide clinical input to decisions impacting image quality, quantification accuracy, dose, and user experience.
Participate in evaluation of AI‑enabled Nuclear Medicine and PET-CT, supporting clinical validation and performance claims.
Contribute to usability, clinical validation, and regulatory‑related documentation as required.

As part of our companys Point of Care Ultrasound business, this role focuses on activities that contribute to the design and development of innovative ultrasound products and their interaction with the human body. You will play a key part in planning and executing tasks that impact departmental operations, ensuring compliance with standard functional practices and procedures. While the position offers some autonomy, it is primarily centered on delivering high-quality execution within an established operating discipline. Some judgment may be required, offering guidance to other team members.
Join us in transforming patient care by bringing advanced imaging closer to clinicians- helping them make faster, more accurate decisions when it matters most.
Job Description
Roles and Responsibilities
Technical Product Leader
Design and define clinical applications- AI tools, clinical and workflows applications, according to user needs communicated by product managers, clinical team, field feedback and physicians.
Project management collaborating with multifunctional teams: software, algorithms, system, program, mechanics, UX\UI designer, verification, clinical team and product managers.
Documentation of product requirements- design input and output.
Review verification plans and procedures.
External evaluation sites support.
Regulatory submission support.

we are seeking a Lead Systems Engineer with a strong background in electronics and a solid understanding of electronic systems to drive Point-of-Care Ultrasound systems engineering activities across the full product lifecycle.
Job Description
Key Responsibilities:
Lead and manage system-level requirements and specifications throughout product development
Drive system verification and validation activities, including end-to-end system testing
Act as the primary interface between Algorithm, Software, and Verification & Validation (V&V) teams
Lead product risk management activities in accordance with regulatory and quality standards
Drive resolution of complex technical issues to ensure project milestones and goals are met
Collaborate closely with Program Management to support scheduling, mitigate technical risks, and inform decision-making through sound engineering judgment.

The Clinical Applications Specialist MICT brings deep Clinical Education expertise with Molecular Imaging and Computed Tomography (MICT) product knowledge to support both pre-sales and post-sales activities. This position is responsible for delivering high-quality clinical training, supporting product demonstrations, and contributing to the success of MICT system installations. The role also includes customer engagement strategies, ensuring that company MICT solutions are used to their full clinical and operational potential.
**This is a one-year fixed-term position with the possibility of extension, subject to business needs and performance.
Job Description
Key Responsibilities:
Deliver comprehensive clinical applications training (on-site and remote) to MICT users, ensuring safe, effective, and optimized use of our company MICT systems.
Provide technical and clinical leadership during the sales process by showcasing product features, clinical benefits, and workflow integration.
Support the Sales team with product demonstrations, clinical evaluations, and customer presentations tailored to specific clinical needs.
Coordinate installation and initial training activities with Sales, Service, and Clinical Education teams to ensure smooth customer onboarding experience.
Monitor customer installations and provide ongoing education and optimization support to enhance user proficiency and satisfaction.
Promote our companys MICT differentiators, including advanced imaging capabilities, AI-driven features, and workflow innovations.
Participate in trade shows, workshops, and customer visits, delivering product demonstrations and educational sessions.
Document training sessions, site visits, and customer interactions in accordance with local compliance protocols.
Support the adoption of digital tools and contribute to the digital transformation of clinical education and customer support.
Act as a liaison between customers and internal teams (Sales, Marketing, R&D) to provide feedback and identify opportunities for product and service improvement.
Stay current on industry trends, competitor offerings, and emerging clinical practices in MICT.

The Project Manager leads a cross-functional/multidisciplinary team of Leaders and their respective project teams for PET programs in Haifa, to deliver project objectives., The program manager drives clarity by continuously defining and prioritizing work, defines the critical success factors/deliverables for the team.
Job Description
Duties include (but are not limited to):
1. Overall responsibility for program success providing engineering innovation within time, budgetary, quality and performance constraints and guidance to continuously deliver products directly supporting the overall business strategy.
2. Creates and ensures effective and efficient communication across business functions.
3. Applies leadership to motivate and energize the variety of cross-functional teams consisting of the program.
4. Works closely and transparently with Product Leadership and Business Leadership to align program with market dynamics and drive program direction.
5. Leads cross-functional and/or multi-disciplinary program planning, drives the team to generate trade-offs and identify and manage risks from the early planning phase, throughout the entire program execution.
6. Works as an equal partner with the program team to deliver results, understands and openly supports all functional goals.
7. Solves complex and ambiguous problems, leads the strategic and forward-thinking program execution including (but not limited to) concept discussion, program execution, rollout, training, pilot trials, clinical evaluations until successful deployment to serial production.
8. Works with customers to solicit input and feedback to meet quality and customer expectations.
9. Provides expert guidance and support to the program organization in various technical/functional aspects.
10. Creates and supports the stewardship of intellectual property with appropriate security of project documentation.

We are seeking an experienced Senior Software Engineer to join our team in Haifa. The role focuses on designing and developing high-quality, performance-critical software in modern C++ for complex healthcare systems. The ideal candidate brings strong hands-on C++ expertise, solid software engineering fundamentals, and the ability to work effectively across software, hardware, product, and verification teams. Experience in embedded or hardware-integrated systems is a strong advantage.
Job Description
Responsibilities
Design, develop, and maintain robust software components in modern C++.
Own features and technical tasks from requirements and design through implementation, integration, testing, and release.
Participate in software architecture, technical design discussions, and code reviews.
Develop reliable multithreaded and performance-sensitive software.
Investigate complex software and system issues, identify root causes, and implement sustainable solutions.
Integrate software with hardware, devices, algorithms, and other system components.
Write clean, maintainable, testable, and well-documented code.
Collaborate with cross-functional teams, including system engineering, AI/algorithm, product, and verification.
Mentor engineers and contribute to engineering practices and knowledge sharing.

We are seeking an experienced and self-driven Senior Mechanical Engineer to join our Ultrasound Point of Care (POC) R&D team. In this role, you will be responsible for leading the mechanical design, development, verification, and transition to manufacturing (NPI) of compact ultrasound systems, consoles, and system accessories.
This position emphasizes complete end-to-end mechanical ownership-from initial conceptual design, detailed CAD modeling, and DFM to collaborating with external subcontractors, managing tooling approvals, and ensuring seamless integration on the manufacturing line.
Job Description
Key Responsibilities
Mechanical Design & Engineering: Drive the mechanical design and electronics packaging of compact ultrasound hardware, consoles, suspended masses, sheet metal structures, and custom system accessories from initial concept through mass production.
Subcontractor & Vendor Collaboration: Collaborate with external subcontractors, injection molding suppliers, tooling vendors, and design agencies (including overseas suppliers in China and globally) to ensure design feasibility and quality.
DFM & Production Readiness: Oversee Design for Manufacturability (DFM) reviews, tool design approvals, sample inspections, and root-cause analysis for plastic injection parts, metal forming, castings, and extrusions.
Design Control & Documentation: Author and maintain technical documentation, including System/Mechanical Requirements Specifications (DRS), Verification Protocols (VPR, VRS), Engineering Change Requests/Orders (ECR/ECO), assembly drawings, and Bill of Materials (BOM).
Compliance & Standards: Ensure mechanical design compliance with medical device standards, cleaning & disinfection guidelines (ISO 17664), system labeling, and environmental/regulatory requirements.
Testing & Assembly Line Support: Design test fixtures, write verification plans, execute mechanical testing, and provide real-time engineering support to assembly floors and production lines.