לוח משרות דרושים מהנדס חשמל לדוברי אנגלית, לחיפוש זה נמצאו 19 משרות

we are looking for a Application Engineer.
In this position, you will engage in pre-sale technical activities while supporting existing customers.
You will respond to technical inquiries, reproduce and investigate complex issues across a wide range of domains in close collaboration with the R&D team, and drive effective resolutions. You will design and implement customer-facing demo and reference applications in C++, develop AI applications that showcase our products capabilities at major industry events such as CES and other trade shows, and provide knowledge transfer to our FAEs to strengthen field enablement and customer success.
Responsibilities:
Understand the customers technical use case for technology and the customers system comprehensively.
Develop a comprehensive understanding of each customers technical use case and system architecture, leveraging this knowledge to effectively support R&D in analyzing and resolving issues.
Serve as a subject matter expert on VPU product, maintaining deep knowledge of product features and the roadmap in order to support FAEs and Tier-1 customers.
Lead technical alignment processes with customers by clearly communicating status, addressing questions and requests, and coordinating responsibilities across the company.
Master technical messaging to effectively support business development and sales activities.
Design and implement demo applications when needed and occasionally participate onsite in customer demos or engagements.
Collaborate closely with R&D, Product, and Business teams to achieve key business milestones and drive new product requirements based on customer needs.

we are looking to hire an experienced, motivated and skilled Embedded Software Engineer to join our software group in Tel Aviv. As a team member, you will be responsible for low-level software stack and infrastructure, focusing on Linux kernel and driver development, real-time firmware development. The teams responsibilities include various aspects such as pre- and post-silicon development, security considerations, power & memory management across different processors in a real-time environment. If you are excited about tackling challenging low-level problems and leading difficult technical problems independently, we want to meet you!
Responsibilities:
Play a crucial role in leading technical projects or software chip development from scratch, driving technical execution and integration with full independence.
Help build and develop our best-in-class Edge AI SoC from the ground up, all the way from a Proof-of-Concept to a leading product.
Develop in different software environments, including embedded Linux kernel development, low-level drivers, and real-time firmware.
Work closely with the hardware team, integrating and debugging complex hardware/software systems from a deep understanding of the various chip IPs while considering challenging system requirements as part of managing a large-scale embedded system.

We are seeking a highly motivated and experienced Sr. Production and Quality Engineer to drive exceptional product quality, patient safety, and field reliability across the Installed Base (IB). This is a key technical role supporting production stability, RMA/DOA investigations, Automated Test Equipment (ATE) performance, and cross-functional quality engineering initiatives in a regulated medical device environment
Key Responsibilities
In this role, you will
Support RMA/DOA processes and continuous reduction of field failures.
Support qualifications and control of ATE testers in production lines.
Support ECO/ECR processes, NPI projects, product updates, and cross-functional engineering changes.
Work closely with R&D, engineering, manufacturing, and operations teams to enhance product quality and resolve technical issues.
Drive continuous improvement initiatives using tools such as Six Sigma, Lean, and Root Cause Analysis (RCA).
Participate in supplier selection and conduct suppliers audits.
Ensure compliance with ISO 13485, FDA 21 CFR 820, MDR, and other applicable medical device regulations.
Maintain and support quality documentation, including CAPA, Non-Conformance Reports (NCRs), and risk management documentation.