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Landa invites you to join an innovative and dynamic R&D team, working on leading-edge industrial presses. As an Inkjet System Engineer, you will work on cutting-edge inkjet systems while collaborating with multi-disciplinary teams in designing, developing, and optimizing print heads' operating conditions and maintenance systems.

Responsibilities:

* Ability to clarify & translate product & marketing requirements into system requirements.
* Planning and executing experiments involving inkjet print heads, ink delivery systems, and printhead support systems in Landa R&D presses and inkjet lab.
* Perform Large data sets analysis and reporting.
* Develop Diagnostic tools.
* Design the tests, validate, and approve the implementation.
* Data mining & analytical capabilities
* Lead methodological problem-solving and escalations from customers and within the organization.
* Receive and proactively seek field and production feedback, drive ongoing product improvements, and identify performance and capability enhancement opportunities.
* Extract SW/control and system modification requirements.


Attributes:

* Interpersonal skills and excellent teamwork - the ability to meet technical and human challenges.
* Ability to lead research assignments independently.
* Ability to lead without authority, Assertive and proactive.
* Fluent in Hebrew and English

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.

We are looking for a talented R&D Mechanical Engineer. to join our innovative medical device company.
In this role, you will be responsible for developing surgical and transcatheter devices to help cardiovascular patients, you will understand the need and the operating environment (anatomy and Cath lab) as well as the ability to thrive in a collaborative team environment.
If you are passionate about making a difference in the lives of patients and thrive in a fast-paced, dynamic environment, we would love to hear from you!
What will you do?
Create, test, and/or improve products by developing complex experiments and tests (including writing and executing protocols), analyze results, make recommendations, and develop reports, based on engineering principles
Generate work instructions, test methods, engineering models and drawings/prototypes, etc., to establish/characterize product and/or process specifications
Create/update more complex design control documents including requirement specs, and risk documents
Develop and execute engineering project plans
Identify, evaluate, manage, and provide guidance to suppliers, including establishing tolerances and defining acceptance criteria for suppliers
Assign R&D support tasks; give instruction to technicians on conducting tests; train technicians and provide feedback; and coordinate technician work
Evaluate input and form a technical recommendation including designing parts, components and subsystems
Train, coach, and guide lower level employees on routine procedures

Make a meaningful difference to patients around the world.
The Edwards Israel Innovation Center (EIIC) focuses on developing early-stage cardiovascular technologies for structural heart disease.
Our passion, ingenuity, collaboration, and new ways of thinking enable us to develop devices and therapies that help patients around the world.
Our teams create the tools, technologies, and devices that transform patients lives.
As part of our assembly teams, your attention to detail and commitment to continuous improvement will help us turn innovative ideas into reality.
Your purpose-driven work will help leave lasting and positive impacts on patient lives.
How you will make in impact:
Taking part in developing processes.
Assembly of valves and other devices under microscope for consecutive period of times.
Working in a controlled environment.
Solutions preparation.
Taking part in sterilization processes.
General lab work.

We invest a significant proportion of our revenue towards research and development to drive and develop groundbreaking medical innovations for structural heart disease and critical care.
As part of our R&D Engineering team, you will work closely with our Quality and Manufacturing teams to develop the latest tools and technologies to address significant, unmet clinical needs that impact patients lives around the world.
About Us:
Aortic stenosis impacts millions of people globally, yet it often remains under-diagnosed and under-treated.
Edwards groundbreaking work in transcatheter aortic heart valve replacement (TAVR) pioneered an innovative, life-changing solution for patients by offering heart valve replacement without the need for open heart surgery.
Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. Its our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.
How you will make an impact:
Develop core products which involve mechanical, bio-medical and other fields
Use SolidWorks to design components, assemblies and fixtures and generate drawings to manufacturing level.
Design and conduct experiments including generating protocols and reports, analyze data using statistical techniques (DOE Design of experiment) and develop test methods.
Use analytical tools (e.g. FEA, CFD) to support design and testing of metallic, Polymers and soft components
Generate work instructions, test methods, engineering drawings/prototypes, etc., to establish /characterize product and/or process specifications.
Give clear instruction to technicians on conducting tests, assembly, and other tasks.

Highly skilled and motivated Quality Design Engineer to join our dynamic team in the medical device industry.

The ideal candidate will have a strong background in design control, quality assurance, and regulatory compliance, with the ability to work collaboratively with R&D, Engineering, Regulatory and other teams.
Adaptable and possess a deep understanding of the regulatory landscape governing medical devices, specifically experience in all phases of product life cycle (design, development, risk management, design verification, production) in adherence with ISO13485:2016, 21 CFR 820 and ISO14971.
Main Duties:
- Lead and implement design control and production processes to ensure compliance with industry standards and regulations.
- Lead proactive design assurance activities facilitating the development and release of high-quality products.
- Collaborate with cross-functional teams to integrate quality into the design and development and manufacturing process.
- Stay abreast of evolving regulatory requirements for medical devices and ensure the company's adherence to relevant standards.
- Work closely with R&D teams to understand design requirements and provide quality engineering input throughout the product development lifecycle.
- Conduct design reviews to identify and address potential quality issues early in the process.
- Responsible for reviewing, providing input and approving product development DHF documentation (design planning, inputs and outputs, design review, V&V protocol -reports, risk analysis, and design change, product transfer to operations, etc).
- Responsible for approval of product design changes and process changes (ECO).
- Participate in Design Reviews for product teams as the quality expert, reviewer, and approver.
- Implement risk management processes and methodologies in the design and development phases per ISO 14971.
- Participate in risk assessments and develop strategies to mitigate potential risks.
- Establish and maintain quality assurance procedures to ensure product quality and regulatory compliance.
- Conduct audits and assessments to identify areas for improvement and implement corrective actions.
- Conduct Failure investigations for Complaints and CAPA.
- Responsible for approval of equipment qualification and process validation documents (pFMEA, IQ, OQ, PQ, etc).
- Perform supplier audits and provided support in preparation and performance of external audits to ensure quality and regulatory requirements are met.
- Support continuous improvement activities to reduce product failure rates.