לוח משרות דרושים מהנדסים בחיפה וסביבתה, לחיפוש זה נמצאו 860 משרות

We are looking for a Technical support to join our growing robotics startup. This role is hands-on and multidisciplinary, involving installation, maintenance, troubleshooting, and on-site support of complex robotic systems. The systems combine mechanics, hardware, electronics, and advanced software, and require strong system-level understanding. The position includes work at our companys facilities as well as international travel, primarily for system installations, demos, and field troubleshooting. As part of our rapidly growing, small, motivated, and multi-disciplinary team, this position is the first dedicated role in its domain, providing a unique opportunity to contribute to a new area within the company.

Responsibilities
Maintain, test, and troubleshoot robotic systems at the companys facilities.
Install, calibrate, and commission robotic systems at customer and partner sites abroad.
Lead on-site system setup and troubleshooting during demos and early deployments.
Diagnose and resolve hardware, mechanical, and software issues in the field
Perform hands-on replacement and repair of mechanical and electromechanical components.
Work closely with R&D teams (software, mechanical, electrical, algorithms) to deeply understand the system.
Gather knowledge from internal engineering teams and apply it independently in the field.
Provide technical feedback from the field to improve system robustness and usability.
Document issues, procedures, and best practices.

We are looking for a hands-on Mechanical Engineer to join our R&D team and contribute to the development of an advanced robotic platform for ophthalmic surgery.

The role involves designing, developing, and testing precision mechanisms and test systems as part of a complex, multidisciplinary medical device.

You will collaborate closely with engineers across multiple disciplines and take ownership throughout the development lifecycle-from initial concept and detailed design through prototyping, integration, testing, and transfer to production.

Responsibilities
Design and develop mechanisms, assemblies, and test rigs throughout the product development lifecycle-from concept generation and detailed design through prototyping, integration, verification, and transfer to production.
Design mechanical solutions incorporating motors, sensors, bearings, gears, and other precision components.
Develop and execute mechanical tests and experiments to evaluate design performance and verify engineering requirements.
Prepare and maintain engineering documentation, including drawings, calculations, test protocols, reports, and engineering change documentation.
Collaborate closely with systems, software, electronics, manufacturing, quality, and operations teams to develop multidisciplinary solutions.
Support hands-on prototype assembly, integration, troubleshooting, and testing.
Identify mechanical design challenges and develop practical, data-driven solutions.
Contribute to design reviews and the continuous improvement of products and development processes.

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.

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.

The Algorithm Software Engineer will contribute to the design, implementation, testing, and performance optimization of tomographic image reconstruction software for our company Molecular Imaging scanners.
This is an exciting opportunity for an outstanding early-career engineer to work at the intersection of software, algorithms, high-performance computing, and medical imaging. We are looking for exceptional graduates with strong technical foundations, intellectual curiosity, and the ability to solve complex problems.
No prior professional experience is required. Academic, research, personal, or internship projects demonstrating strong technical capabilities are highly valued.
Job Description
Roles and Responsibilities
Develop and implement reconstruction algorithms and software tools in C++ within parallel CPU/GPU environments.
Collaborate with algorithm engineers and scientists to understand mathematical and physical algorithms and translate them into robust software solutions.
Contribute to the architecture and design of complex software components.
Collaborate with software teams to define interfaces between the reconstruction environment and other software subsystems.
Analyze and optimize software performance, runtime, and memory usage.
Write software requirements, design documents, and technical specifications.
Design and execute software unit tests.
Support the Verification & Validation team in defining and executing system testing plans.
Support technical investigations and field-related issues as needed.
Participate in code reviews and technical reviews.
Maintain configuration management and control of generated code.
Continuously learn and apply new technologies in software engineering, algorithms, and high-performance computing.