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We are looking for an innovative R&D Mechanical Design Engineer to join Our Mechanical Department!
Job description:
Managing the mechanical design of projects under development, from concept to completion.
Responsible for mechanics risk management and mitigation processes.
Executing the mechanical design of plastic parts and assisting throughout the mold production.
In charge of performing and documenting tests.
Performing design improvements and supporting production lines.

we are seeking for a V&V Engineer, to join the QA, RA & CA department.
As a V&V Engineer, your principal task will be to verify and validate Medical Devices. You will be responsible for HW & System testing including test protocols and reports.
The main responsibilities within this role:
Design, develop and execute system Verification and Validation test procedures.
Responsible for writing detailed, comprehensive, and well-structured V&V test protocols and reports ensuring requirements coverage and traceability.
Analyzing issues and failures in the system.
Work in a highly multidisciplinary and complex technical environment and lead testing of cross-functional projects (with emphasis on mechanical and electro-optical aspects)
Being involved in the reliability and integration tests for prototypes under development
Coordination and management with external testing laboratories
Define and maintain the Verification & Validation plans.
Plan and arrange the work, schedules, and equipment required for testing and evaluating standard and special devices.
Identify, investigate, and document all findings raised during testing.
Work closely with cross functional team members including R&D (System, SW&HW), QA, RA and Product departments.

we aim to improve patient outcomes by empowering every gastroenterologist across the globe with artificial intelligence and disruptive therapeutic technologies.

In this exciting role as an Operation Quality Engineer, you will directly support the day-to-day Yokneam products manufacturing, transfer, and improvements activities. You will have the opportunity to drive a culture of continuous improvement by deploying sound engineering fundamentals to achieve quality objectives and ultimately yielding better patient outcomes.

A Day in the Life
Communicate quality standards and requirements within the organization and collaborate with engineering and manufacturing functions to ensure quality standards are in place. Devise and implement methods and procedures for inspecting, testing, and evaluating the precision and accuracy of products and production equipment.
Oversee and participate change approval process (risk assessment, verification, validation).
Lead Quality Assurance and product quality improvements in cross-functional initiatives. Ensure that corrective measures meet acceptable reliability standards, and that documentation is compliant with requirements.
Collaborate with global Operations, QA, Engineering and Manufacturing to ensure quality standards are in place and support day-to-day manufacturing activities.
Specialize in the areas of production control, incoming material, product evaluation, and reliability, inventory control, and development as they apply to product or process quality.
Take an active role in leading and reviewing design and manufacturing changes and lead product quality investigations in support of CAPA, complaints and non-conforming material processes and lead Quality Assurance and product quality improvements in cross-functional initiatives.

* Jigs design
* Drawing & technical documents updates
* NPI processes
* Subcontractors support.
* Dealing with multiple interfaces
* Working with suppliers
* Development of test equipment
* Equipment & product Validation

The adaptation of trailers to accommodate imaging systems requires working with customized trailer providers who are experienced with this type of vehicles.

The work involves engineering and project coordination activities aimed releasing new offerings of PET/CT and SPECT/CT in a mobile setup according to GEHC requirements.

Design activities would consist of layout of the various scanner subsystems to accommodate a mobile installation, design of supporting brackets and other parts as needed, definition and execution of thermal, vibrations, safety, acoustic tests and road tests to qualify the integrated scanner to trailer solution for clinical use; creating the safety documentation related to the mobile specific configuration, create the supporting engineering documentation required to release the integrated solution and formally release the engineering change (ECO).

Project coordination activities would include setting a workplan in place, tracking the tasks, setting the pace, and communicating progress to a variety of stakeholders engineering functions, program managers, and product managers.

Each such mobile configuration is unique and considered to be a project which requires management of its tasks and interfacing with various functions inside GEHC and with the trailer provider.

Essential responsibilities:

Mechanical design of parts and assemblies derived from the need to install the MI systems inside the trailer. This includes customized parts for the mobile specific installation,
Creating and maintaining the BoM related to the installed systems via ECR/ECO process,
Building safety files for products by executing the calculations required to provide safe and effective installation of the various sub-systems inside the trailer (gantry, chiller, power units, cables, etc.). These include mainly the definitions of the anchorage for the system due to dynamic forces and heat load and heat removal requirements.
Participating with the trailer provider company in the definition of the system layout inside the trailer to provide clear and safe access for the patient, operators, and service personnel, while accounting for the service requirements during preventive maintenance or other service procedures.
Participate in the definition and monitoring of the testing required to certify the trailer according to GEHC internal standards and other local country regulations when applicable. This includes communication with testing providers, mainly in the USA.
Communicate with GEHC internal external function related to the mobile configurations. This includes system and other R&D engineers, program leadership and representatives of the trailer company engineering and other functions.