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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.

The Production Engineer is responsible for defining, maintaining, and continuously improving production processes to ensure quality, efficiency, and scalability. The role focuses on process ownership, implementation of engineering methodologies, and supporting stable production while enabling yield, cycle time, and cost improvements.
Key Responsibilities
Own and maintain production processes, process flows, and work instructions.
Define and implement production engineering methodologies to improve quality, yield, and efficiency.
Provide daily engineering support to production lines, including hands-on troubleshooting.
Lead root cause analysis for process-related issues and implement corrective and preventive actions.
Drive yield improvement, scrap reduction, and cycle time optimization initiatives.
Support introduction of new products and processes in collaboration with NPI and R&D teams.
Define process parameters, control plans, and acceptance criteria.
Lead process validation, qualification, and change management activities (ECO).
Collaborate with Quality to ensure compliance with internal and customer requirements.
Support production ramp-up, line balancing, and capacity planning activities.
Work with Maintenance and Test Engineering to ensure equipment and test readiness.
Drive standardization and best practices across production lines.

we are looking for a Test Equipment design and Maintenance Engineer.
Job Description:
Define test specifications, acceptance criteria, limits, and control methods based on product and quality requirements.
Support design, validation, and release of new test fixtures, jigs, and automated test systems.
Function as the technical owner for new production testing requirements.
Define, implement, and maintain preventive, predictive, and corrective maintenance activities for production and test equipment.
Own maintenance plans, schedules, checklists, and work instructions.
Monitor equipment performance, analyze downtime, and lead root cause analysis and corrective actions.
Provide hands-on troubleshooting and engineering support to production lines.
Own test-related documentation, change management (ECO), and version control.
Support production ramp-up, yield improvement, and test stability activities.
Drive continuous improvement initiatives for equipment reliability, test robustness, and maintenance efficiency.
Collaborate closely with Production, Process Engineering, NPI, Quality, and external vendors

The NPI (New Product Introduction) Engineer is responsible for ensuring a seamless transition of new products from development to full-scale production. This role involves:
Production Line Setup: Design and implement new production lines, including defining jigs, fixtures, and automated processes.
Global Line Duplication: Duplicate existing production lines in overseas facilities (Far East), requiring strong planning and coordination skills.
Process Qualification: Validate and optimize production processes to ensure efficiency, quality, and compliance.
Project Management: Lead end-to-end NPI transfer projects, covering layout planning, process design, supply chain coordination, and quality assurance until changes are released through the ECO process.
Failure Analysis: Investigate and resolve production issues to maintain continuous operations.
Cross-Functional Collaboration: Work closely with R&D, project managers, quality, planning, and purchasing teams to achieve production goals.
Job Responsibilities
Design and implement new production lines, including jigs, fixtures, and automation.
Validate and optimize manufacturing processes for efficiency and quality.
Lead end-to-end NPI transfer projects, from layout planning to ECO release.
Conduct failure analysis and resolve production issues promptly.
Collaborate with R&D, project management, quality, planning, and purchasing teams.
Duplicate existing production lines in overseas facilities (Far East).
Coordinate global implementation and ensure alignment with company standards.
Travel internationally for extended periods to support line duplication and setup.

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.