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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

This hybrid position is based in Yokneam, Israel/Santa Clara, California/ Lafayette, Colorado facilities. The role requires occasional travel and involves independent work to maintain quality standards across global operations.
Responsibilities may include the following and other duties may be assigned:

Provide oversight for development and maintenance of quality management systems, ensuring full compliance with FDA, ISO 13485, and other regulatory requirements
Lead audit and inspection preparation activities, coordinate with regulatory bodies, and manage resolution of findings through comprehensive Corrective and Preventive Actions (CAPA)
Conduct process analysis and risk assessments to identify improvement opportunities and ensure adherence to quality standards across manufacturing and design operations
Collaborate with cross-functional teams to interpret regulatory requirements and implement quality policies that support our endoscopy and surgical device portfolios
Prepare detailed quality reports and documentation for internal stakeholders and external regulatory agencies
Facilitate global quality standards implementation and best practice sharing across international sites

R41483