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Our smART+ platform is a sensor-based feeding system for intensive care unit (ICU) patients. It aims to prevent life-threatening complications such as ventilator-associated pneumonia, malnutrition, and acute kidney injury. We recently introduced Nutrition Management 2.0, which is a comprehensive, guideline-driven approach that aims to improve nutrition while reducing feeding complications. Combined with our smART+ platform, it monitors, analyzes, and prevents malnutrition and gastric aspirations in real time. By improving nutrition and achieving 100% feeding efficiency, the smART+ platform greatly reduces hospital-acquired complications and speeds up ICU patient recovery. We are looking for an R&D Electronic Technician to join our interdisciplinary group of hardware, firmware and software engineers. Key Responsibilities:
* Perform manual testing on complex, integrated hardware and software medical systems, designing and writing TEST documents
* Level 4 component level repairs, reading electrical drawings, loading / burning components and operating simulation software.
*  Technical Support for the development team and assistance in debugging software and hardware
* Support for field trials.
* Ongoing work with system engineers and development teams.

We are searching for a QA member to be a part of our talented team. As part of the role you will participate in all testing cycle, from design to tests execution in our unique projects. Our QA team is open to embrace a new way of thinking and method of testing.

Responsibilities:
As a QA Engineer, You Will: Be a part of QA processes, execute manual end-to-end testing Partner with Software Development and System Engineers on new designs and features and customer requirements Take ownership of quality health (e.g. testing coverage, performance, best practices, etc.) Innovate on testing tools, quality, and team processes.

Embedded QA Engineers primary responsibilities will include but are not limited to:

55% Design, Develop, Test, Document and Maintain Test setups, Test scripts and Software Applications to Troubleshoot, Diagnose or Qualify software and hardware components of the tablets.
40% Maintain expert level of product knowledge and applications to provide product support and training to customers and partners.
Understand field technology, systems, and applications to contribute to the support team in product training, troubleshooting and procedures.
Resolve customer issues or difficulties in a manner that is consistent with the company mission, values, and financial objectives.
Research, Identify, Develop, Document and Recommend corrective measures to address technical issues identified in the field or in-house.
5% Work closely with internal engineering teams to ensure that they are meeting the customers needs and be a liaison to the customer.

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.

Required Supply Chain Manager.
DESCRIPTION:
Responsibility for strategic planning, optimization and policy setting for the management of supply chain activity, inventory sourcing and spare parts procurement.
Includes the management of the supply chain of the home appliance sector in the company, including:
- Managing the subcontractors abroad and in Israel.
- Managing customer orders and coordinate supplies with sales department.
- Work with internal interfaces in developing, NPI and ODM.
- Inventory control and optimization of quantities, analysis inventory needs and forecast inventory levels.
- Handling supply chain processes and managing process from the development stage including product pricing and closing process with external and internal parties.
- Warehouse managing and inventory counting.
- Constant streamlining and improvement of processes and work methods.
- Responding and solving problems in the supply chain processes.

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.

We are looking for a Clinical Affairs Manager to implement and oversee all activities related to clinical research and clinical studies in the company.
DiA Imaging Analysis provides AI-powered solutions to make ultrasound image analysis smarter and more accessible.
Its AI-based solutions help ultrasound users acquire the right image and analyze it automatically, allowing them to identify clinical abnormalities that are often difficult to find visually and enabling them to make better decisions based on accurate and objective data.
Your role:
Designing and managing the execution of clinical studies that demonstrate medical product safety and efficacy.
Ensuring that trials are conducted in full compliance to GCP.
Full responsibility on sites initiation, site personnel training and monitoring.
Working closely with the principal investigators and study coordinators.
Working with regulatory, development and marketing teams to create scientific publications, clinical marketing material and clinical background required for regulatory submissions.

דרוש/ה פיזיקאי/ת חוקר/ת פוטוניקה (Photonics Researcher) לחברת מוליכים למחצה בת"א
We are looking for exceptional talent to join our Photonics team as a Photonic Scientist, involved with fundamental aspects of the development of a state-of-the-art solid-state laser.
Responsibilities:
Mapping-out material and performance related limitations of our laser
Offering and testing design improvements to reduce the above limitations
Reviewing related literature and building hypotheses through simplified physical models
Planning and executing experiments to validate hypotheses
Consult team members and work together to research/production/productization activities.
Proposing and testing design solutions / new architectures to improve the product in terms of performance, manufacturability, cost, size and reliability

Its a rare opportunity to develop new products, especially large and strategic investments in a well-established organization. If youve been waiting for that kind of opportunity to come along, this may be the career opportunity for you.     
The Identity and Network Access team is searching for software engineers across all disciplines, who can define, build, and evolve heavily integrated platforms at scale. Our team is part of the Security organization in and is responsible for bringing networking, identity, and security together. In these times, where working from anywhere has never been more important, it is our set of services that enables people around the world to stay productive every day, while still meeting companies security and compliance needs.  Our cloud services are built to solve these challenges for our customers in a seamless and integrated stack as we constantly push ourselves to stay at the cutting edge of the industry.  
We're beyond excited to share we have just announced a brand new product. a fusion of networking, identity, and security solutions.
Introducing Entra Internet Access comes to protect web, SaaS applications and 365 applications, setting rules and policies to control and avoid outside threats.
Entra Private Access protects access to private networks of the organization and gives access to the relevant employees from any network or device.
By granting organizations the authority to set precise policies for specific applications, we substantially diminish the risk of unauthorized access to valuable organizational resources.
This is a broad cross-team role with high visibility. You will collaborate closely with multiple teams across Microsoft to deliver key customer solutions and the technology to support them.

Lead design and implementation of the future architecture for highly scalable, durable, low latency systems.
Build an effective and agile development organization using industry leading best practices.
Lead the definition of requirements, KPIs, priorities and planning of engineering deliverables.
Proven team building experience as well as mentoring and growing team members.
We believe in enabling our team members to unlock their highest potential and invest a lot in building a collaborative and agile culture to achieve our business success. Join us and be part of our path to the next level of awesomeness