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Eitan Medical is a fast-growing global medical device company, developing and manufacturing innovative infusion solutions across the continuum of care- from the hospital to the home. We are seeking an experienced Manufacturing Engineering Manager to join our team and report directly to the COO. The Team leader will manage all Engineering activities, employees, and projects, ranging from Design Transfer and cost reduction to production stability. The Team leader will be a significant member of the Operations management team. Job Description: 1. Manages the day-to-day activities of the Engineering team as well as the management and execution of team’s projects against project plans and company goals. 2. Provides guidance and direction, as well as hands-on resource and project management, for all Engineering activities. 3. Optimizes the manufacturing lines, continuously support and improve efficiency, quality, and safety. 4. Analyse and resolve process issues, ensuring consistent and reliable production output. 5. Organize manufacturing validation activities for new and existing products to ensure product specifications and procedures are achieved. 6. Lead investigations of manufacturing deviations (NCMR) and process failures and identify root causes that will lead to applicable corrective actions. 7. Work closely with R&D on product deviations investigations and troubleshooting resulted from the production line. 8. Extending process and product Engineering controls to outsourced manufacturing of administration sets (single use sterile products), ensuring alignment with company standards and regulatory requirements. 9. Managing design transfer processes from design freeze to the implementation of stable and validated production line. 10. Lead Engineering changes (ECO) and process experiments. 11. Provide guidance on the Engineering workshop activities, including equipment/ fixtures (Jigs) purchasing, calibration and maintenance. 12. Collaborate with cross-functional teams, including R&D, manufacturing, quality, and supply chain, to implement process corrective actions and improvements. 13. Supporting the Quality and production departments as needed. 14. Proactively leads cost reduction initiatives and supports operational excellence projects.

a global leader in smart energy technology. We invite you to join our own manufacturing in the north of Israel. By being Solaredge's Process Engineer you will you will have great opportunity to be involve in building a new Engineering system. What will you be doing?
* Follow up the process control for complete life cycle of the product.
* Control the process flow / routing on the Manufacturing system and the production floor.
* Lead process improvements on production site.
* Knowledge of ECO/DEV on the production floor and production system.
* Focal point / Expert for technical, engineering related for the production team.
* Implement of new technology, engineering change at the production site with cooperation with different department in the company.

we are a fast-growing medical device company focused on developing, manufacturing, and selling innovative devices for endovascular interventional procedures.= We are seeking a skilled and detail-oriented QA Engineer to join our team. The ideal candidate will be responsible for executing Quality Assurance activities, managing quality projects, and participating in process and product validations to ensure compliance with established standards and regulatory requirements. The QA Engineer will work closely with cross-functional teams to support quality projects, provide manufacturing support, and drive continuous improvement initiatives across the organization. LOCATION: Yokneam, Israel. The position includes the following responsibilities: SCOPE & RESPONSIBILITIES Manage ECOs: conduct risk assessment, 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. Ensuring 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.

Abra is hiring a PMO! The role includes developing and maintaining integrated work plans, risk management, bottleneck analysis, budget planning and control, and more. This is a full-time position, Monday to Friday, in Be'er Ya'akov.

ABRA is Hiring a Planner Job Description:
* Executing MRP runs , analyzing requirements, and procuring complex BOMs
* Creating purchase requests and work orders for production.
* Ongoing monitoring and control of procurement and production processes Location: Full-time position, Sunday-Thursday , in Be’er Ya’akov