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We are now looking for a Chip Design Verification Engineer. We are seeking a verification engineer to join the chip design methodologies team. The team is in charge of the verification methodologies, shared code, training, and embracing new technologies. One of our main goals is to make sure that the team works in an efficient manner, and provides high-quality deliveries. This position offers the opportunity to have real impact in a dynamic, technology-focused company.

What you'll be doing:
Develop shared verification code and solutions to be widely used by the chip design team.
Develop groundbreaking methodologies to create a flawless experience for verification engineers to keep the focus on new problems.
Collaborate with the design automation team to provide end-to-end solutions that combine verification, simulation, and automation.
Get in touch with EDA vendors to learn about cutting-edge tools/technology and apply them into our verification process.
Understand the design, define the verification scope, develop the verification infrastructure and verify the correctness of the design.
Collaborate with designers, verification specialists to accomplish your tasks.
Develop training sessions.

Post Market R&D team is seeking a highly skilled, experienced, and versatile Software Engineer to maintain and enhance released products and developing innovative, high-quality solutions addressing field, regulatory, cybersecurity, and market needs.
The primary focus of this role is Windows Desktop software development, including applications, tools, services, installers, and utilities for medical products and medical applications.
The ideal candidate brings a strong and broad software engineering background, with a proven ability to contribute across multiple software domains such Web, Cloud , DevOps and CI/CD.
As part of Global company, 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:
Windows Desktop Software Development: Design, develop, maintain, and enhance Windows-based desktop applications, tools, services, installers, and utilities.
Debugging & Troubleshooting: Diagnose and resolve issues in products and applications.
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, complying medical standards.
Security & Compliance: Conduct security assessments and ensure adherence to medical software standards. Maintain SBOMs (Software Bill of Materials)
DevOps & CI/CD: Contribute to DevOps activities, CI/CD pipelines, automation and utilities. Develop automation tools and scripts using Python and PowerShell.

As a Quality Engineer in Manufacturing, you will play a key role in ensuring that products are manufactured in compliance with internal quality standards, regulatory requirements, and our companys commitment to patient safety and product excellence. This position partners closely with Manufacturing, Operations, R&D, and Supply Chain to drive quality improvements and support continuous improvement initiatives on the production floor.
Responsibilities may include the following and other duties may be assigned:
Provide quality engineering support for manufacturing operations and engineering.
Support production, engineering, validation activities including training, reviewing and approving documentation, work instructions, SOPs , supporting risk assessments, to ensure compliance with regulatory and quality system requirements.
Lead and support investigations of nonconformances, deviations, and CAPAs, including root cause analysis and implementation of corrective and preventive actions.
Collaborate with cross-functional teams to identify, assess, and mitigate quality risks in manufacturing processes.
Support internal and external audits, including preparation, participation, and follow-up on audit findings.
Drive continuous improvement initiatives using quality and lean methodologies.
Ensure effective implementation and monitoring of process controls and quality metrics.
Support change management activities ensuring requirements are identified and executed when applicable.
Participate in Management Review and Quality Metrics reporting.

This role at our company Yokneam is responsible for designing, optimizing, and sustaining manufacturing processes in a highly regulated medical device environment. The position partners closely with Production, Quality, and R&D to drive operational excellence, implement MPS methodologies, and improve key operational KPIs such as yield, quality, and OEE, while ensuring full compliance throughout the product lifecycle.
Responsibilities may include the following and other duties may be assigned:
Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling.
Designs arrangement of machines within plant facilities to ensure most efficient and productive layout.
Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance.
Develops manufacturing processes that are applicable to statistical process control, and may develop those techniques.
Provides guidance to engineering regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques.
Ensures processes and procedures are in compliance with regulations.
Monitors documentation maintenance throughout all phases of product lifecycle.
Drives a continuous improvement mindset by engraining and improving the MPS (our company Performance System) methodologies in the day-to-day.
Main contact with Operations Innovation and region improvement team.
Execute Improvement in Yokneam Operations KPIs (Yields, Quality, OEE).
Acts as a partner with mainly production and Quality operations and other functions in Operations and R&D sustain team.