לוח משרות דרושים ייצור ותעשייה בשרון, לחיפוש זה נמצאו 588 משרות

We are looking for a talented Mechanical Engineer to join the R&D Incubation team on a temporary basis. In this role, you will contribute to the early-stage design and development of innovative cardiovascular technologies in the TAVI (Transcatheter Aortic Valve Implantation) space. You will be responsible for concept development, laboratory testing, and collaboration with internal stakeholders and external manufacturing partners.
How you will make an impact:
Develop and iterate early-stage mechanical concepts and prototypes for transcatheter cardiovascular devices
Plan, execute, analyze, and report bench testing
Create and maintain 3D models, engineering drawings, and technical documentation using SolidWorks
Coordinate with external vendors and contract manufacturers on component fabrication and delivery
Collaborate closely with the THV Incubation Manager and cross-site engineering teams (Israel & Irvine)
Support design reviews, project milestones, and technical documentation as required.

our company, a Sisram Medical company, is a global leader in medical-aesthetic technologies, with over 25 years of experience in energy-based devices (EBD). Over the years, our company has evolved into an integrated aesthetic and wellness ecosystem that combines medical devices, injectables, diagnostics, and personalized skincare. The company operates in a dynamic, innovation-driven environment, merging advanced technology with deep clinical understanding to create holistic solutions for aesthetic clinics. our companys headquarters are in Caesarea, Israel, with business operations in more than 100 countries worldwide.
* Establish, build, and lead the V&V team from the ground up, including defining methodologies, processes, and best practices
* Manage and mentor a small and growing team of V&V engineers
* Lead end to end, comprehensive verification and validation activities for multidisciplinary medical devices, combining technologies such as laser, RF, ultrasound, and physics-based systems
*  Define, author, and execute rigorous TEST strategies, validation plans, and protocols for complex systems
* Ensure full compliance with medical device regulatory standards, including documentation, traceability, and validation processes
* Partner closely with matrixed cross-functional teams including Mechanics, Hardware, Software, system Engineering, Regulatory, Clinical and Quality
* Drive continuous improvement of TEST methodologies, modern tools, and automation capabilities
* Support end-to-end product lifecycle activities including design verification, system validation, and post-market activities.
* Partner with Operations and NPI (New Product Introduction) groups to ensure seamless transfer from design verification to manufacturing line validation
* Manage relationships and scheduling with External Certified TEST Houses for safety, EMC, and environmental compliance testing

we are a global pioneer of our systems for active military protection, counter-drone applications, critical infrastructure protection, and border surveillance. We are looking for an experienced Program Manager to join our team. Job Description: Overall responsibility for managing, maintaining, and continuously improving the organizations Quality Management system (QMS), including certification processes, internal and external audits, regulatory activities, and compliance oversight, while ensuring alignment with organizational objectives, applicable standards, procedures, customer requirements, and relevant compliance obligations. Key Responsibilities:
* Lead and manage the organizations Quality Management system (QMS) end-to-end across development, project management, operations, and production.
* Ensure the establishment, implementation, maintenance, and continuous improvement of quality processes, procedures, and controls in alignment with applicable standards and organizational requirements.
* Manage and develop the quality and regulatory team, providing professional leadership across quality, regulatory, and compliance activities.
* Oversee certification activities, internal and external audits, and the effective management of nonconformities, corrective actions, and preventive actions.
* Lead regulatory and compliance activities to ensure adherence to applicable requirements, customer expectations, and organizational commitments.
* Monitor performance through quality metrics and management reporting, and drive a culture of quality, accountability, and continuous improvement across the organization.