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As a Mechanical Design Engineer, you will be responsible for the design, development, and validation of mechanical components and systems for our diverse product line, focusing on innovation and manufacturability. This role offers the opportunity to contribute directly to the advancement of sustainable energy solutions. Responsibilities:
* Design and develop robust and reliable mechanical solutions for electronic packaging, particularly for high-power outdoor products, considering thermal management, environmental protection, and manufacturability.
* Design components optimized for various manufacturing processes, including plastic injection molding, die casting, extrusion, and sheet metal fabrication.
* Collaborate with electrical engineers on the mechanical integration of printed circuit boards (PCBs) within product enclosures.
* Create and maintain detailed production documentation, including mechanical drawings, assembly instructions, and PCB layouts, ensuring accuracy and completeness.
* Review First Article Inspection (FAI) reports, analyze results, and approve parts for mass production, ensuring adherence to quality standards.
* Perform engineering calculations (e.g., stress analysis, heat transfer analysis, magnetic simulations, dynamic analysis) to validate designs and ensure performance requirements are met.
* Participate in design reviews, contribute to problem-solving, and drive continuous improvement in design processes.
* Collaborate with cross-functional teams, including product management, manufacturing, and testing, to ensure successful product development and launch.
* Contribute to the validation, testing, and troubleshooting of mechanical components and systems throughout the product development lifecycle.
Country:
Israel
City:
Herzliya

we are looking for a Assembler II.
Responsibilities may include the following and other duties may be assigned.
Performs a variety of tasks ranging from repetitive to non-repetitive production assembly operations.
Works from visual aids, method layouts, diagrams, schematics, process flow sheets and written or verbal assembly instructions.
Sets initial layouts, and uses a variety of tools to prepare product(s).
Makes continuity checks on work in process and completed.
May conduct quality inspections on processing line in accordance with quality specifications.
May disassemble, modify, rework, reassemble, and test experimental or prototype assemblies and subassemblies according to specifications and under simulated conditions.
R57572

You will be an integral part of the team that supports the companys quality policy to Put Patients First. This team collaborates with global teams to support products across several portfolios. This is a flexible role where the employee is at a minimum 3 days a week on site in the office with option of remote working for 2 days in the week.
Responsibilities may include the following and other duties may be assigned:
Develops, modifies, applies and maintains quality processes and protocols to support servicing of reusable medical devices
Collaborates with engineering and operations functions to ensure quality requirements are in place and met
Devises and implements methods and procedures for processes related to servicing of medical devices
Supports and/or leads audits and inspections from the auditee perspective for service processes in quality management systems
Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
Supports and/or leads projects to improve compliance or standardize service and repair related processes
R57831

we are a fast-growing global medical device company, developing and manufacturing innovative drug delivery and infusion solutions across the continuum of care- from the hospital to the home. We are looking for an excellent Production Quality Engineer to join the QA product team Job Description:
* Serve as owner of the NCMR process: manage the end-to-end handling of non-conforming materials, products, and processes, including initiation, investigation and corrective/preventive actions in accordance with company procedures and regulatory requirements.
* Monitor NCMR process including quality KPIs
* Support for non-conformity investigations and assign effective corrective actions for NCMRs and ensure timely closure and documentation.
* Perform / review Root Cause Analysis as part of NCMR process and assign relevant corrective actions.
* Act as QA representative for Manufacturing Quality process
* Conduct Quality Assurance activities such as data analysis and statistical evaluations, SOP review and approvals, audit preparation Direct Manager: Manufacturing Quality Manager