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Join our engineering team as a Process Engineer and help drive meaningful improvements across our manufacturing operations. In this role, you will lead opportunities to enhance efficiency, quality, and safety while working closely with cross-functional teams to solve problems and optimize processes. This is an exciting opportunity for a motivated engineer who enjoys hands-on impact, continuous improvement, and contributing to a high-performing environment. If you are looking for a role where your ideas can make a real difference, we encourage you to apply.
This position is on-site working based at our company Yokneam. You will report to the engineering manager and collaborate regularly with teams across production, quality, maintenance, and operations. Some travel may be required to support other sites, project work, or training initiatives. The role offers the chance to work in a fast-paced environment with strong opportunities for learning, development, and career growth.
Primary Responsibilities
Responsible for all manufacturing processes on production floor, pFMEA, Equipment URS, Working instructions, test methods, Support production training, Define Packaging instructions; Ensures processes and procedures are following regulations; Monitors documentation maintenance throughout all phases of product lifecycle.
Project management skills, Responsible for timelines, Scop of work, Budget.
Implement jigs, fixtures, and other manufacturing support tools for medical device assembly and testing.
Improve manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling; Review arrangement of machines within plant facilities to ensure most efficient and productive layout.
Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance.
Support manufacturing processes that are applicable to statistical process control, and may develop those techniques; Issue specification requirements to best utilize equipment and manufacturing techniques.
Drives a continuous improvement mindset by engraining and improving the MPS (our company Performance System) methodologies in the day-to-day; Execute Improvement in Yokneam Operations KPIs (Yields, Scrap, Quality, Safety, OEE).
Acts as a partner with mainly production and Quality operations and other functions in Operations and R&D sustain team.

Eitan Medical is a fast-growing global medical device company, developing and manufacturing innovative drug delivery and infusion solutions across the continuum of care: from the hospital to the home. As part of our growth and commitment to innovation, we are expanding our R&D department and looking for a Senior Mechanical Engineer to join our Mechanical team in the R&D department. Join us as we continue to grow and make a meaningful impact on healthcare worldwide Mechanical design and development of multidisciplinary medical devices, primarily infusion pumps and related accessories, with a focus on mechanism development and compact electro-mechanical packaging. Lead the mechanical aspects of the design and development of new products, from concept through production, while providing ongoing engineering support for the company’s existing product portfolio
Direct Manager Mechanics & HW Director

we are looking for a CTO Integrator.
The CTO Integrator plays a key role in planning, building, and conducting tests of jigs for experiments. This position involves designing, building, and integrating test systems to ensure experiments meet their required specifications and physical phenomena.
Responsibilities:
Jig Construction and Testing: Build and integrate jigs, then conduct tests to ensure they function as required.
Test Design: Design and develop tests for experiments in a research and development environment.
Simulation Verification: Ensure that test jigs simulate the necessary physical phenomena for accurate testing.
Technology Assessment: Examine new technologies, run tests, and analyze data for potential integration.
Collaboration with Researchers: Work closely with researchers to ensure test systems align with experimental needs.

we are looking for a System Operator.
The System Operator is responsible for operating and maintaining Digital Casting production systems in an R&D environment, working in an industrial setting under the supervision of a process engineer. The role involves working in 3 shifts: morning, evening, and night.
Responsibilities:
Machine Setup: Assemble tools and load raw materials into machines, preparing them for operation.
Calibration: Perform required calibrations to ensure proper machine functioning.
Process Monitoring: Check and input process parameters and other production data.
Equipment Operation: Operate equipment for material handling and the computerized process.
System Performance Monitoring: Monitor and report on operational equipment, ensuring optimal system performance.
Data Recording: Record process-related data in an organized manner for accurate tracking.
Quality Inspections: Perform visual inspections of quality and quantity, making adjustments to resolve issues under supervision.
System Cleanup: Disassemble cast parts and clean the system after processing at the end of each shift.
Safety Compliance: Adhere to all safety requirements and properly use personal protective equipment (PPE).
Inventory Management: Maintain and manage inventory of materials and tools.

we are looking for a QC Engineer.
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).

The Configuration Control Engineer is responsible for managing configuration control and product build processes within the PLM system. This role involves documenting products throughout their lifecycle, collaborating with R&D, marketing, manufacturing, and subcontractors.

Key Responsibilities:

Oversee configuration control and product release in the PLM system.
Document products throughout their lifecycle, working closely with R&D, marketing, manufacturing, logistics, QA and subcontractors.
NPI- Support products from development through to mass production.
Integrate manufacturability and testability considerations (DFM, DFA, DFT, DFC) during design reviews.
Provide technical support related to PCB topics.
Oversee First Article production and feedback for corrections.
Define manufacturing processes, prepare instructions, assembly drawings, and related documentation (Manufacturing procedures, Fabrication flow, PRR, etc.).
Manage engineering change processes in PLM-ORACLE.
Collaborate with various company departments and interfaces.
Build manufacturing files and support subcontractors (including supporting production line issues).
Optimize production lines and improve engineering processes using new technologies, cost reduction, and time-saving initiatives.
Write procedures and ECR/ECN documents

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 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.

As a Software Engineer - PET Data Acquisition, you will join a highly specialized team developing the real-time software stack at the core of our companys PET/CT imaging systems.
Our software directly impacts image quality and system reliability, enabling clinicians worldwide to provide accurate diagnoses and life-saving care.
You will work on a distributed, high-performance C++ system running on Linux, responsible for configuring detector hardware, processing high-throughput data streams, and enabling seamless integration across the scanner ecosystem.
Job Description
About the Team
Our team develops the data acquisition platform powering our companys PET/CT scanners.
This system:
Configures and interfaces with detector hardware
Receives high-rate event streams via UDP
Performs real-time sorting and time-stamping of coincidence events
Manages acquisition state and persistence
Exposes control and monitoring APIs to clinical applications
The platform is a distributed, multi-process, multi-threaded C++ system running on Linux, designed for deterministic, high-performance operation under demanding workloads.
Key Responsibilities
Design and develop end-to-end data acquisition features, from low-level UDP capture and event processing through service layers and client APIs
Optimize and maintain performance-critical code paths, including:
Lock-free / low-contention data structures
Thread affinity and NUMA optimization
Zero-copy buffer management
Deterministic real-time execution
Enhance and maintain inter-process communication mechanisms, including shared memory, message queues, and service interfaces
Work with embedded persistence layers (SQL-based) for configuration, metadata, and runtime state
Collaborate closely with hardware, physics, and system teams to integrate new detector and system components
Develop unit and integration tests, and actively participate in code and design reviews
Troubleshoot complex cross-process issues using advanced debugging and profiling tools (e.g., gdb, perf, tcpdump, strace).

This position refers to leading the design of parts and assemblies for the company imaging systems (PET, SPECT). The position includes working inside an NPI project or supporting the systems in the field (Install Base). The mechanical design of parts and assemblies includes working with multi-disciplinary teams including electronics, system engineering, service engineering and involves transfer of designs to production, support of high-level-assembly lines, etc. This position involves the writing of safety files, planning and execution of V&V tests, engineering calculations and FEA simulations, writing specifications and failure analysis.
Job Description
Essential responsibilities:
Mechanical design derived from specifications (as well as writing specifications), as part of a multi-disciplinary team of parts and assemblies while using off-the-shelf components, using 3D CREO CAD design package. Presenting the design in technical design reviews at the levels of concept and detail design is a part of this position,
Developing creative design solutions in response to the product requirements of functionality, reliability, cost, manufacturability, etc.,
Support of company products at hospital and customer sites via the Service Teams as needed,
Building safety files for products, including strength calculations, failure modes analysis (FMEA), compliance with safety and medical industrial standards as well as internal company standards,
Supporting transfer to production, defining basic assembly and service instructions, working with parts suppliers,
Defining verification and validation test procedure, tests execution and report writing.
Essential qualifications /requirements:
Mandatory: 1st degree in mechanical engineering
Mandatory: Good personal, teamwork and communication skills, enthusiasm from study, self-motivated, results oriented,
Work experience of 2 years in mechanical design, with experience in at least 2 of the following: design of motion systems, large welded or cast structures and frames, mechanisms, electronic packaging, large sculptured FRP covers, electrical design support (DXF, cables routing),
Experience in machining and sheet metal technologies,
Experience in prototype building (hands on), testing execution per test plan and failures troubleshooting
Fluent English at presentation level in technical design reviews, Zoom/Teams calls and in writing.
Desired Characteristics by priority:
Leading tasks from requirements to engineering change finalization,
System level understanding in multi-disciplinary project environment,
Definition of testing and report writing,
Experience in design for cost, reliability, serviceability and for manufacturability.
Ability to perform finite-element analysis and Excel level technical calculations,
we are a leading global medical technology and digital solutions innovator. Our mission is to improve lives in the moments that matter. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.