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Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Essential Functions
Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Collaborate and liaise with study team members for project execution support as appropriate.
If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

The Engineering Technician is part of our company's Operations and Manufacturing function, supporting the production of medical devices used by healthcare providers and patients worldwide. The team partners with engineering and manufacturing groups to maintain equipment performance, support process improvements, and ensure reliable, high-quality production operations.
The Engineering Technician provides hands-on technical support for manufacturing equipment, production processes, and engineering initiatives. This role partners with engineers and operations teams to troubleshoot equipment issues, support process optimization activities, and help maintain safe, efficient, and compliant manufacturing operations.
This is a temporary (1-year contract), on-site position based in Yokneam.
Primary Responsibilities:
Provide technical support for manufacturing equipment, processes, and engineering projects.
Troubleshoot equipment, instrumentation, and process issues to minimize production downtime.
Monitor equipment performance and collect operational, calibration, inspection, testing, and repair data.
Perform technical investigations and resolve equipment malfunctions and process deviations.
Support process improvement initiatives focused on yield, cycle time, quality, safety, and cost.
Assist with implementation and sustainment of 5S and visual management activities.
Support workstation organization, material flow improvements, and workplace standardization.
Contribute to production line layout optimization and productivity improvement projects.

The Engineering Technician is part of our company's Operations and Manufacturing function, supporting the production of medical devices used by healthcare providers and patients worldwide. The team partners with engineering and manufacturing groups to maintain equipment performance, support process improvements, and ensure reliable, high-quality production operations.
The Engineering Technician provides hands-on technical support for manufacturing equipment, production processes, and engineering initiatives. This role partners with engineers and operations teams to troubleshoot equipment issues, support process optimization activities, and help maintain safe, efficient, and compliant manufacturing operations.
This is a temporary (1-year contract), on-site position based in Yokneam.
Primary Responsibilities:
Provide technical support for manufacturing equipment, processes, and engineering projects.
Troubleshoot equipment, instrumentation, and process issues to minimize production downtime.
Monitor equipment performance and collect operational, calibration, inspection, testing, and repair data.
Perform technical investigations and resolve equipment malfunctions and process deviations.
Support process improvement initiatives focused on yield, cycle time, quality, safety, and cost.
Assist with implementation and sustainment of 5S and visual management activities.
Support workstation organization, material flow improvements, and workplace standardization.
Contribute to production line layout optimization and productivity improvement projects.

The Manufacturing Engineering function supports the development, transfer, and optimization of manufacturing processes for medical device products. The team partners closely with Operations, Quality, R&D, Supply Chain, and Production to implement scalable manufacturing solutions, improve process performance, and support business growth through operational excellence.
As a Senior Manufacturing Engineer, you will lead and support manufacturing process development, process improvements, equipment implementation, and production support activities. This role is responsible for driving manufacturing efficiency, product quality, and compliance while serving as a technical expert across cross-functional projects and operational initiatives. This position is based in Yokneam and follows an onsite work model.
Primary Responsibilities:
Lead the design, development, validation, and optimization of manufacturing processes and production methods.
Develop and implement manufacturing solutions that improve product quality, yield, throughput, and cost performance.
Design and optimize production layouts, equipment configurations, and material flow to maximize operational efficiency.
Evaluate manufacturing equipment performance, identify process gaps, and implement corrective and preventive actions.
Partner with R&D, Quality, and Operations teams to support product introductions, design transfers, and design-for-manufacturing initiatives.
Develop and maintain manufacturing documentation, work instructions, process specifications, and validation protocols.
Apply statistical process control and data analysis techniques to monitor and improve process capability.
Provide technical leadership, mentoring, and project support to manufacturing engineering teams and cross-functional stakeholders.

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 companys Surgical Operating Unit is a new, powerful operating unit bringing together the people and product portfolio of Surgical Robotics and Surgical Innovations. With the company 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.
As a Sr Software Engineer, you will design, develop, test, and deploy software solutions for complex products and systems. You will collaborate across software, hardware, systems, and algorithm teams, taking technical ownership of features and solutions from architecture and design through deployment and support
Primary Responsibilities
Design, develop, test, and maintain software applications using modern .NET and C# technologies.
Develop, optimize, and support software running on Linux-based systems.
Collaborate with software, hardware, systems, and algorithm engineering teams to deliver integrated solutions.
Design and implement cloud-native architectures using KEDA for scalable workloads and Terraform for infrastructure automation
Troubleshoot and resolve software issues across development, testing, and production environments.
Build, deploy, and maintain Docker-based containerized applications.
Drive technical decisions and own solutions from architecture and implementation through deployment and lifecycle support.
Contribute to code reviews, testing strategies, and software quality initiatives.

We are looking for a Windows platform expert with deep, hands-on scripting skills (PowerShell preferred) to own the security hardening, imaging, and deployment automation of the Windows environment underlying our FFRangio system.
You'll work at the intersection of low-level Windows internals (boot security, disk encryption, image management) and modern Windows virtualization and DevOps practices (CI/CD pipelines), helping us build a secure, locked down, and reliably reproducible Windows environment for a regulated medical device product.
You should be comfortable going deep - from BIOS settings and TPM chains up through image-building and pipeline automation - and who treats scripting as the primary tool for making security and deployment repeatable, auditable, and reliable, in service of a real clinical product used in the Cath lab.
Responsibilities may include the following and other duties may be assigned:
Design, implement, and maintain PowerShell-based automation for system configuration, hardening, and deployment of FFRangio Windows workstations
Define and enforce BIOS/UEFI security settings and TPM-based trust chains (Secure Boot, measured boot, TPM attestation)
Implement and manage BitLocker and other Windows encryption mechanisms, including key management and recovery strategies
Build and maintain Windows hardening baselines using Group Policy, AppLocker, custom Shell/UI restrictions, and Kiosk (Assigned Access) mode suited to a clinical, cath-lab environment
Manage user/account permission models and least-privilege access schemes across managed devices
Create, manipulate, and maintain VHD/VHDX-based images for deployment, recovery, and testing workflows
Build and maintain CI/CD pipelines in Azure DevOps for automated build, test, and deployment of Windows images and configurations
Collaborate with software, QA, and regulatory/quality teams to ensure hardening and deployment practices
Document configurations, scripts, and processes for reproducibility and audit purposes, consistent with medical device quality system requirements.

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.