לוח משרות דרושים ייצור ותעשייה בחיפה וסביבתה

We are seeking a highly skilled and motivated Mechanical Systems Engineer to join our Silicon Photonics Engineering team in Haifa, Israel. This role supports the development of advanced micro-mechanical and macro-automation systems for photonics and semiconductor test equipment. You will collaborate globally, reporting to the SiPh Engineering Manager in North Reading, MA, USA.



In this role, you will design and develop precision mechanical systems that enable high-performance optical and semiconductor testing. Your work will directly support the rapid growth of AI and integrated photonics technologies.



Design micro-mechanical systems using 3D CAD tools such as NX, AutoCAD, or SolidWorks
Develop micro-actuation hardware for photonic integrated circuit (PIC) optical connections, including fiber-to-chip and connector-to-receptacle interfaces
Engineer macro-automation solutions for integrated circuit (IC) handling from JEDEC trays
Model and characterize complex mechanical systems using FEA tools such as COMSOL or Ansys (preferred)
Use structural analysis and CAD tools to architect new modules and evaluate performance and limitations
Define and implement critical metrics and specifications aligned with product requirements and characterization methods
Influence product-level decisions through simulation, prototyping, and lab-based validation
Build custom unit tests and metrology hardware; perform hands-on measurements in the lab
Collaborate with suppliers to develop actuation modules, bring up test platforms, and conduct statistical analysis of performance and quality
Travel to supplier sites to support engineering builds and assist in failure analysis activities

We are seeking a highly motivated and collaborative Mechanical Engineer to support our Silicon Photonics Engineering group in Haifa, Israel. Development occurs in a dynamic and challenging global multi-site environment. This role will report to the SiPh Engineering Manager in North Reading, MA, USA.



You will lead and/or participate in platform product development initiatives within our Silicon Photonics product team. In the SiPh Engineering group, we focus on developing state-of-the-art Optical Instruments for our Semiconductor Test Equipment products. This optical test equipment is essential for the massive expansion in AI that the industry is currently experiencing.



You will create innovative and sound technical solutions to complex engineering problems. You will also identify essential requirements and key technical risks. You will work closely with Electrical Engineers, Systems Engineers, and Optical Engineers to design solutions for New Product Introduction and High-Volume Manufacturing.



Develop detailed mechanical designs using 3D CAD, along with creating 2D fabrication drawings
Create Engineering Change & Release documents (ECN / ECO)
Participate in internal design reviews
Work with Systems Engineering team to help define sub-systems, establish technical direction, and develop product strategies and long-term product roadmaps
Build, debug, and test prototype designs
Assist NPI team with the build and debug of customer early access units
Collaboration with procurement & supply chain to identify alternative vendors and suppliers

This Quality Documentation & Training Coordinator is responsible for implementation and execution of documentation, change control, and training processes based on business, regulatory and customer requirements to ensure compliance with company and regulatory requirements.
This role will be based in Haifa following our planned office relocation in 2026.
Duties & Responsibilities
Initiates and executes an effective and efficient change control process in accordance to internal procedures
Lead, facilitate, and mentor teams through all stages of the change control and training process
Leads and participates in quality system improvement initiatives
Interface between functions /departments such as Design, Quality and Operations in product, process, system, or supplier related changes
Have responsibility for initiation of changes, assessment of the change impact and routing of all tasks, with attention to detail, for completeness, accuracy, effectivity and appropriateness
Liaise with Change Requester and SMEs during all stages of the Change Control process, including Training process
Reviews all changes for ensuring sound rationale, challenging justification, correct approval, alignment and oversight
Monitoring completion of post release tasks to ensure completion in a timely manner
Support and lead initiatives for continuous improvement
Participate in project teams for change control
Support in training needs related to the change control process
Manages periodic review process and procedures in applicable PLM Systems.
Support in the preparation, participate, and address issues related to document and change management for internal and external (FDA, BSI, etc.) audits as needed
Investigates and resolves non-conformances, audit observations, corrective and preventive actions (CAPAs) related to Change control and training process
Assists in the creation and development of metrics to evaluate the effectiveness and efficiency of Change Control Processes
May support onboarding training for new employees; collaborate with managers to align onboarding content with role-specific needs.
Monitor training completion, generate compliance reports, and collaborate with stakeholders to ensure compliance.
Performs other duties assigned as needed.

Joining us is a chance for you to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, more than 4,000 of us are challenging whats possible and making headway to help improve outcomes.
The Senior Engineer I - LCM, Testers & Calibration systems is responsible for extending the longevity, reliability, and compliance of Testers & Calibration systems across production, supplier, and R&D environments. This includes leading technical initiatives, managing system upgrades, supporting production and customer issues, and driving continuous improvement projects.
This role will be based in Haifa following our planned office relocation in 2026.
Responsibilities
Manage Life Cycle activities for Testers & Calibration systems, including End-of-Life (EOL) planning and upgrades.
Lead Proof of Design (POD) activities for hardware, software, and process updates.
Develop and improve production support systems, testers, jigs, tools, and documentation.
Drive Cost Improvement Projects (CIP) focused on yield, quality, efficiency, and data management.
Provide system engineering expertise and calibration guidance.
Lead configuration control and spare parts strategy.
Execute Engineering Change Orders (ECOs) and ensure quality of system engineering deliverables.
Initiate and manage CAPA activities related to yield and customer feedback.
Solve technical issues and analyze system data.
Ensure compliance with company and regulatory standards.

Joining us is a chance for you to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, more than 4,000 of us are challenging whats possible and making headway to help improve outcomes.
The Quality Engineer II oversees the execution of the quality plans ensuring product realization is conducted in compliance with internal, customer and regulatory requirements during all phases of the product lifecycle. Under limited supervision and in accordance with all applicable federal, state and local laws/regulations, procedures and guidelines, this position:
This role will be based in Haifa following our planned office relocation in 2026.
Reviews new and modified product design and manufacturing processes for quality characteristics, including manufacturability, serviceability, testability, reliability and conformance to product and quality system requirements.
Develops and manages the product risk management process, including the development and maintenance of risk management files.
Qualifies component and service suppliers, conducts supplier audits and ensures that appropriate supplier quality controls are implemented.
Analyzes data and applies knowledge of engineering principles and practices to implement continuous improvement projects.
Provides guidance to R&D, Operations and Quality on design and production/process controls, risk management, root cause analysis, validation and the application of statistical methods.
Host business meetings with other functions within the organization including but not limited to Training, Human Resources, Manufacturing and Research and Development.
May manage projects that involve other functions within the organization including but not limited to Training, Human Resources, Manufacturing and Research and Development.
Responsible for communicating business related issues or opportunities to the next management level.
Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.
For those who supervise or manage staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable.
Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
Performs other duties assigned as needed.

We are looking for a highly motivated and experienced Senior Verification Engineer to perform and guide design verification for the electro-mechanical portions of the system design.
For this role, were focusing on electrical and mechanical parts, assembly and functional aspects of the system design. This is an ideal opportunity for someone who is motivated and passionate to make an impact in leading the development of the next generation of ophthalmic robotic surgery.
Responsibilities
Create verification protocols based on electromechanical design input requirements.
Identify applicable standards for each electromechanical aspect and define how they are addressed in verification activities.
Establish statistical sample sizes according to the risk level associated with each part, assembly, and feature.
Lead protocol development and test execution for sterilization validation.
Guide a team of verification engineers and testers in creating test protocols, executing tests, reviewing results, and generating reports.
Participate as a team member in the development of new features related to electromechanical assemblies and associated robotic capabilities.

we are a fast-growing medical device company focused on developing, manufacturing, and selling innovative devices for endovascular interventional procedures. Were looking for a QA Engineer to support and strengthen our manufacturing quality. In this role, youll work closely with cross-functional teams, execute day-to-day quality activities on the manufacturing floor and help drive continuous improvement in a hands-on, fast-paced environment.
LOCATION: Yokneam, Israel.
SCOPE & RESPONSIBILITIES
* Manage ECOs: conduct risk assessments, update relevant DMR documents and carry out necessary IQ, OQ, PQ activities if required, finalization of implementation tasks.
* Manage DCOs in the PLM system : Write and update QA procedures to ensure compliance with quality standards and regulatory requirements.
* Manage NCR and CAPA processes: Lead, write and supervise the NCR and CAPA processes, ensuring timely and effective resolutions.
* Manage QA production activities: Provide quality support to production operations, addressing deviations and non-conformities to maintain high product quality.
* Ensure Timely Resolution of Quality Issues: Promptly address all identified or assigned quality issues to prevent delays and maintain efficient operations.
* Participate in audits: Take part in internal and external audits, such as FDA inspections and notified body audits based on ISO13485, EUMDR, and MDSAP requirements.
* Manage Supplier quality: Manage supplier qualification and performance monitoring, including SCAR management, and support supplier audits.