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Our products reshape how data is processed and used on a global scale, and were looking for the brightest people to join us.

We are looking for talented and ambitious individuals to join our Hardware team.

Roles and responsibilities:
Definition, design, and production of Chain Reaction reference designs and internal prototyping and evaluation HW.
Product specifications.
Electrical schematics.
Component selection.
Layout guidance.
Hands-on development and testing in a lab environment.
Accompanying production and qualification processes.

Our products reshape how data is processed and used on a global scale, and were looking for the brightest people to join us.

We are looking for Analog Layout Engineer.

Roles and responsibilities
Layout design of sensitive analog circuits where you will need to bring state-of-the-art solutions.
In close co-operation with the Circuit Designer, review and analyze complex analog schematics for layout implementation.
Ensures layout designs best functionality and quality by performing all relevant checks like parasitic checks, IR drop and Electromigration, noise and DFM.
Perform post-layout iterations to ensure the best results.

Post Market R&D team is seeking a highly skilled, experienced, and versatile Firmware / Software Engineer to maintain and enhance firmware for released products and develop innovative solutions addressing field, regulatory, cybersecurity, and market needs.

You will design and deliver low-level software across multiple platformsranging from bare‑metal implementations to RTOS/Linux‑based systemswhile collaborating with hardware, systems, quality, and product teams to ship robust, secure, and compliant firmware for medical and industrial devices.
While the primary focus is on embedded systems and firmware development, we are looking for a candidate who can adapt across multiple software domains, including Windows application development. The ideal candidate will have deep expertise in embedded systems development and a versatile software development background, with a proven ability to contribute across software domains, including Windows development.
Our Medtronic site in Yokneam has a rich product portfolio and we provide solutions that helps our patients alleviate pain, restore health, and extend life.
Responsibilities may include the following and other duties may be assigned:

Firmware Development: Design, develop, and maintain embedded C/C++ firmware for various microcontrollers (e.g., ARM9, MSP430, STM32) and SoCs
Debugging & Troubleshooting: Diagnose and resolve firmware issues using software and hardware debugging tools. Perform validation and troubleshooting using oscilloscopes, logic analyzers, and other test equipment
Cross-Functional Collaboration: Work closely with Hardware, System, QA, and Product teams to meet project goals, Act as the primary technical contact for inquiries and provide ongoing support
Documentation Management: Create and maintain comprehensive Software Development Lifecycle Documentation, including design and verification documents, to ensure alignment with compliance standards
Security & Compliance: Conduct security assessments and ensure adherence to medical device software standards. Maintain SBOMs (Software Bill of Materials) and ensure compliance with medical data standards and regulations
Versatile & Multi-Domain Development: Engage in diverse software domains. Apply your software expertise across both embedded and application-level domains, contributing to Windows desktop software components : Windows-based tools, services, applications, installers and utilities.

R31762

The Manufacturing Team Manager at Rapid-Medical will oversee the NPI and production processes of the Drivewire, ensuring smooth transformation from the development stage to manufacturing, working on high-quality manufacturing standards and efficiency. This role involves managing a team of skilled technicians, driving process improvements, expanding and increasing manufacturing capacity and collaborating with cross-functional teams to enhance efficiency and quality. Responsibilities:
* Oversee the transition from development to full-scale production, including validation, process design, and documentation to ensure successful product launch.
* Lead and manage the Manufacturing Team, ensuring operational efficiency and high-quality output.
* Develop and implement manufacturing strategies to optimize productivity and reduce waste, focusing on continuous improvement.
* Monitor production schedules and adjust resources as necessary to meet customer demands and deadlines.
* Collaborate with R&D to develop new products and improve existing ones, ensuring manufacturability from the onset.
* Establish and maintain safety protocols, ensuring compliance with industry standards and regulations.
* Provide training and mentorship to team members, fostering a culture of teamwork and professional growth.
* Analyze production metrics and prepare reports for upper management to inform strategic decisions.

well give you the opportunity to harness all thats within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, well help you in advancing your skills and career. Here, youll be supported in progressing whatever your ambitions.

About the role:
a worldwide and diverse company who puts patients first. Through this position, the ideal candidate would use their systems engineering and risk management experience to support, develop, establish and maintain Medical Electrical Equipment/Systems (MEE / MES) and associated accessories for New Product Development (NPD) Engineering within the Urology Division of (BSC).
Our team is all about building the future of the operating room for Urologists.

As the industry leader in surgical kidney stone treatment, we are on a mission to empower physicians to treat more cases, more efficiently, with better outcomes; To help patients in need get back to their daily lives. As a Principal Design Quality Assurance (DQA) Engineer, youll be at the heart of that mission to develop and support best-in-class products to bring advanced, safe innovations to the clinic. You will also be leading the effort to develop MEE / MES. Your contributions will directly impact patient care at a company widely regarded as being a quality leader in the medical device industry.

Your responsibilities include:
Lead product teams within the BSC Quality System to develop new MEE and MES as part of a core group of DQA Engineers supporting the Laser Therapies franchise. Special focus on:
Engagement with project teams for Systems Engineering and Systems Risk Management as a Subject Matter Expert (SME).
Utilize Systems Engineering practices to lead efforts for requirements management/system architecture to align risk mitigations with design inputs, design outputs at different levels (e.g., system / sub-system) for products that are both stand alone, and network connected.
Lead NPD projects as a DQA SME and work with R&D Product Development Engineers to review Hardware/Software systems architecture(s) and identify possible failure modes/risk control opportunities for these complex systems.
Lead Risk Management activities during all phases of Electrical HW/SW design, using design quality assurance principles applicable to FDA/EUMDR-Regulated Class II Medical Device environments (including interconnected software systems).
Participate and lead in the creation and maintenance of Risk Management and Usability deliverables.
Lead and/or support development of NPD Reliability Engineering Program Plans and related reliability program activities.
May perform other duties as directed.

General Description:
We are seeking a highly motivated Mechanical Engineer or Process Engineer with strong orientation to machines, to join the engineering team at our company HQ.
This role involves responsibility for defining and improving technological processes, providing technical support to our global production sites, and leading project-based activities including technology transfer from R&D to production and validation processes.
The position includes global support and collaboration with international teams.
Key Responsibilities:
Define, analyze, and optimize manufacturing processes.
Prepare technical documentation for engineering changes.
Plan, execute, and summarize validation activities for processes, equipment, and systems.
Transferring products from development to manufacturing.
Collaborate with global teams to support international operations.

General description:
our company, a global leader in the ophthalmic industry, is looking for an experienced Mechanical Engineer.
This is a great opportunity which allows you to combine technological research & analysis of next generation products, with a strong connection to business and marketing aspects, and a full product lifecycle overview.
Responsibilities:
Take the mechanical engineer role for developing multi-disciplinary systems consisting of mechanics, electronics, optics and software.
Plan and drive research lab hands on activities such as prototyping, platforms bring ups, performance testing, etc.
Generate end to end system analysis and research results reports.
Support production lines of products designed by HQ engineering.