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לפני 5 שעות
חברה חסויה
Location: More than one
Job Type: Full Time and Hybrid work
Position's Scope:
Responsible for driving the transition of complex, multidisciplinary medical devices from design to sustainable serial production through the ECO process, as well as sustaining and optimizing active manufacturing lines.
The scope encompasses process design, yield optimization, system -level troubleshooting (mechanics, electronics), and strict adherence to medical device quality regulations (ISO 13485 / FDA 21 CFR Part 820).

Skills:
BOM maintenance PLM:
High proficiency in drafting technical documents, Standard Operating Procedures (SOPs), and navigating Product Lifecycle Management (PLM) systems for bill of materials (BOM) management.
Multidisciplinary Troubleshooting:
Strong systems-level diagnostic skills to root-cause failures occurring at the intersection of mechanical, electrical, or firmware subsystems.
Requirements:
Minimum of 2+ years of experience as a Manufacturing/Production Engineer within Medical Devices industry
Proven track record of executing Engineering Change Orders (ECOs) within a structured Quality Management system (QMS).
B.Sc. in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, or Manufacturing Engineering from an accredited institution.
Fluent in English Hebrew

Advantage Experience:
Direct experience collaborating with external contract manufacturers (CMs) and suppliers on component and system level quality issues.

Familiarity with Arena and Priority systems
This position is open to all candidates.
 
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8839356
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חברה חסויה
Location: Yokne`am
Job Type: Full Time
We are looking for an NPI Engineer for the R&D team. The NPI Engineer will own the end-to-end transition of multidisciplinary medical devices from R&D prototypes to stable, scalable serial production, serving as the bridge between product development and Operations.

If you want to work in an innovative, international environment and help push the boundaries of healthcare, well-being, and energy-based technology, this is your opportunity!


Key responsibilities:

Lead the full NPI and design-transfer process from R&D handoff through pilot builds, qualification, production ramp-up, and stabilization.

Build and drive transfer plans, schedules, risk and action tracking, production-readiness criteria, and release gates.

Create and maintain the manufacturing package, including BOM/DMR content, drawings, work instructions, test methods, acceptance criteria, tooling, and training materials.

Lead DFM, DFA, and DFT reviews and drive design and process improvements that support quality, manufacturability, serviceability, and cost.

Define, develop, and qualify manufacturing processes, fixtures, equipment, and test setups; prepare and execute validation protocols where applicable.

Lead ECOs and configuration changes, and provide hands-on support for production, yield, quality, field, and obsolescence issues using structured root-cause and corrective-action methods.

Serve as the technical focal point across R&D, Operations, QA/RA, Supply Chain, Service, suppliers, subcontractors, and contract manufacturers.
Requirements:
Requirements:

B.Sc. in Mechanical, Electrical, Biomedical, Mechatronics, or a related engineering discipline.

At least 3 years of experience in NPI, manufacturing engineering, product engineering, or design transfer for multidisciplinary products.

Proven experience supporting pilot and serial production and developing or improving manufacturing processes.

Experience with engineering documentation, BOM/DMR structures, ECO/CO processes, and PLM/PDM and ERP systems.

Strong hands-on troubleshooting, root-cause analysis, and structured problem-solving skills.

Ability to read and interpret engineering drawings, specifications, and technical documentation; SolidWorks experience is preferred.

Fluent Hebrew and English, written and spoken; medical-device or other regulated-industry experience is an advantage.

Education & Experience - Relevant engineering degree and 3+ years of experience in multidisciplinary product industrialization.

Product & Business Acumen - Understands how design choices affect product quality, supply continuity, serviceability, cost, and time to market.

Execution & Leadership - Owns deliverables end to end, prioritizes effectively, and leads cross-functional actions without direct authority.

Communication & Collaboration - Builds strong working relationships and communicates status, risks, and decisions clearly across functions and sites.

Other Requirements - Comfortable working in a dynamic, global, matrix organization and providing hands-on support when needed.

Self-Starter & Problem-Solver - Proactive and resourceful; turns ambiguous technical issues into structured, evidence-based action plans.

Detail-Oriented & Analytical - Uses data, documentation discipline, and sound engineering judgment to ensure repeatable and compliant execution.

Technical Skills - Manufacturing documentation, DFM/DFA/DFT, ECO and configuration control, RCA, process validation, PLM/PDM/ERP, and CAD/SolidWorks.
This position is open to all candidates.
 
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08/09/2026
חברה חסויה
Location: Netanya
Job Type: Full Time
We are a fast-growing international medical device company that develops and manufactures innovative medical equipment. We are looking for a Process Engineer to join our Manufacturing Engineering team. Job Description: The Process Engineer will lead engineering changes and qualify manufacturing processes - on our production floor and at our subcontractors in Israel and abroad - while providing hands-on Technical Support to production. Lead engineering changes (ECOs) end-to-end, from definition and impact assessment, through implementation on the production floor, to formal closure. Plan and execute process verification and validation activities, including IQ/OQ/PQ protocols and reports. Lead process qualification at subcontractors in Israel and abroad, including new and replaced equipment and production lines. Support injection molding activities: DFM reviews with the molder, mold qualification and evaluation of samples. Provide hands-on engineering support to production and final TEST lines, and define jigs, fixtures and process parameters. Conduct technical investigations and root cause analysis as part of the NCMR process, and drive corrective actions to closure. Develop, improve and optimize manufacturing and assembly processes, based on production and yield data. Work closely with Production, Quality, Regulatory, R&D and Purchasing, and manage internal and external stakeholders. Direct Manager: Engineering Manager.
Requirements:
Must Have:
B.Sc. in Engineering - mandatory; Mechanical Engineering - preferred. 3-5 years of experience in Process Engineering, Manufacturing Engineering, or a similar production engineering role. Proven experience leading engineering/process changes end-to-end, from definition through implementation and closure. Experience with process verification, validation, or qualification activities. Experience working with external suppliers and subcontractors. Strong understanding of manufacturing and assembly processes, and proven hands-on experience supporting production. Practical experience using measurement tools and equipment, and the ability to analyze data. Strong problem-solving, investigation, and root cause analysis capabilities. Fluent English - written and verbal, including technical writing
Advantages:
Experience in the medical device industry. Familiarity with FDA, ISO 13485, or other regulated manufacturing environments. Experience with formal process validation protocols and reports (IQ/OQ/PQ). Experience with manufacturing technologies such as injection molding, sheet metal & machining processes. Experience working with, or qualifying processes at, overseas suppliers and subcontractors. SolidWorks/PDM experience and the ability to read mechanical drawings. Experience with eQMS systems. Experience with Lean Manufacturing / Continuous Improvement methodologies. Computer Skills: Proficiency in Microsoft Office applications, with a good level of Excel for data analysis. Personal Skills: Strong technical and analytical capabilities. Hands-on, practical, and solution-oriented approach. Ability to lead cross-functional processes and drive stakeholders to deliver. Excellent interpersonal and communication skills. Self-motivated and independent. Ability to manage multiple priorities and work effectively under pressure. Team player with a proactive and continuous-improvement mindset.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8813745
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לפני 8 שעות
חברה חסויה
Location: Netanya
Job Type: Full Time
A fast-growing international medical device company that develops and manufactures innovative medical equipment. We are looking for a Process Engineer to join our Manufacturing Engineering team.
Job Description:
The Process Engineer will lead engineering changes and qualify manufacturing processes - on our production floor and at our subcontractors in Israel and abroad - while providing hands-on technical support to production.
Lead engineering changes (ECOs) end-to-end, from definition and impact assessment, through implementation on the production floor, to formal closure.
Plan and execute process verification and validation activities, including IQ/OQ/PQ protocols and reports.
Lead process qualification at subcontractors in Israel and abroad, including new and replaced equipment and production lines.
Support injection molding activities: DFM reviews with the molder, mold qualification and evaluation of samples.
Provide hands-on engineering support to production and final test lines, and define jigs, fixtures and process parameters.
Conduct technical investigations and root cause analysis as part of the NCMR process, and drive corrective actions to closure.
Develop, improve and optimize manufacturing and assembly processes, based on production and yield data.
Work closely with Production, Quality, Regulatory, R&D and Purchasing, and manage internal and external stakeholders.
Direct Manager: Engineering Manager.
Requirements:
Must Have:
B.Sc. in Engineering - mandatory; Mechanical Engineering - preferred.
3-5 years of experience in Process Engineering, Manufacturing Engineering, or a similar production engineering role.
Proven experience leading engineering/process changes end-to-end, from definition through implementation and closure.
Experience with process verification, validation, or qualification activities.
Experience working with external suppliers and subcontractors.
Strong understanding of manufacturing and assembly processes, and proven hands-on experience supporting production.
Practical experience using measurement tools and equipment, and the ability to analyze data.
Strong problem-solving, investigation, and root cause analysis capabilities.
Fluent English - written and verbal, including technical writing
Advantages:
Experience in the medical device industry.
Familiarity with FDA, ISO 13485, or other regulated manufacturing environments.
Experience with formal process validation protocols and reports (IQ/OQ/PQ).
Experience with manufacturing technologies such as injection molding, sheet metal & machining processes.
Experience working with, or qualifying processes at, overseas suppliers and subcontractors.
SolidWorks/PDM experience and the ability to read mechanical drawings.
Experience with eQMS systems.
Experience with Lean Manufacturing / Continuous Improvement methodologies.
Computer Skills:
Proficiency in Microsoft Office applications, with a good level of Excel for data analysis.
Personal Skills:
Strong technical and analytical capabilities.
Hands-on, practical, and solution-oriented approach.
Ability to lead cross-functional processes and drive stakeholders to deliver.
Excellent interpersonal and communication skills.
Self-motivated and independent.
Ability to manage multiple priorities and work effectively under pressure.
Team player with a proactive and continuous-improvement mindset.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8838880
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חברה חסויה
Location: Yokne`am
Job Type: Full Time
We are looking for a Technical Project Engineer for the Engineering team. The Technical Project Engineer will be responsible for leading Engineering projects for cost-reduction & sustain engineering

If you want to work in an innovative, international environment and help push the boundaries of healthcare, well-being, and energy-based technology, this is your opportunity!

Main Duties:

Leading Advanced Engineering Projects for Medical multidiscipline system, focusing on value engineering and BOM (Bill of Material) cost-reduction efforts.

Leading E2E (End-2-End) Projects ECO's, from PoC/E (Proof of Concept/Experiment) thought design & Testing (V&V), up to NPI and Production implementation.

Write and Execute Design Verification Testing (V&V) for cost-saving & Sustain engineering projects.

Updating/Creating the BOM & DMR of the System within project in the PLM system.

Write and Execute Manufacturing Validation Testing (PV/MP) from planning through execution & implementation in production sites.

Quality Gate Keeper ensuring overall device safety, efficacy and compliance are withstanding the overall system quality level.
Requirements:
B.Sc. in Electrical/Biomedical/Mechanical Engineering - MUST.

2-4 years Hands-on experienced with Multidisciplinary Medical Equipment V&V Testing - Big Advantage.

Experienced with Laboratory Equipment (Scope, DVM etc.), Problem Solver & technical capabilities - Advantage.

Ability to lead projects including GANTT Timelines, Tracking Tasks, Budget requirements & Project Deliverables.

Ability to Communicate Project Status, Managing Project Weekly Meeting (IPT) and overall communication to superior management.

Ability to work on multiple projects simultaneously with tight deadlines.

Proven leadership skills, quick & self-learner and adaptively/agility abilities.

Technical writing and word processing skills, High level of presentation skills.

Team Player, highly motivated with ambitions to learn.

Familiar with PLM work (Enovia PLM).

Fluent English - Writing and Verbal - MUST.

Valid Driving License + Mobility.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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עדכון קורות החיים לפני שליחה
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תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
7 ימים
חברה חסויה
Location: Yokne`am
Job Type: Full Time
Rapid Medical is a fast-growing medical device company focused on developing, manufacturing, and selling innovative devices for endovascular interventional procedures. We are looking for a talented and creative engineer to join our R&D team and be a key player in our future development. LOCATION: Yokneam, Israel
SCOPE & RESPONSIBILITIES:
* Design and develop innovative neurointerventional medical devices as part of the R&D team.
* Plan and execute verification tests for new prototypes and new products
* Prepare product documentation, including DHF and DMR
* Analyze test results and author detailed engineering reports
* Collaborate with Quality and Regulatory Affairs to ensure design control compliance
* Lead design transfer activities, support pilot production, and transition products into manufacturing
Requirements:
* Bachelor’s degree in Mechanical or Biomedical Engineering from a leading university GPA 85+
* 2-5 years of experience in a relevant engineering role
* Hands-on experience in the medical device industry – an advantage
* Familiarity with design control processes and standards (ISO 13485, FDA 21 CFR 820) – an advantage
* Proficiency with SolidWorks – an advantage
* Full proficiency in English, including reading and writing technical documentation
* Team player with strong communication skills, self-driven and detail-oriented
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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עדכון קורות החיים לפני שליחה
8773679
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2 ימים
Location: Yokne`am
Job Type: Full Time
Our New Product Introduction (NPI) team is growing, and we're looking for a highly motivated and diligent Engineering Vendor Manager to join us. In this critical role, you'll be responsible for the engineering project management of our most strategic and technologically advanced components and suppliers, ensuring on-time delivery of the highest quality and reliability of components for our groundbreaking products.


What you'll be doing:
Manage the product as a project - Define the timeline for having our designs out, manage quality meetings, set full road map for quality, capacity and automation as readiness towards HVM.
Lead engineering engagement with strategic and critical suppliers for new product introductions (NPI) and ongoing production, identify potential risks, critical parameters, and areas for optimization.
Define and implement clear monitoring and documentation requirements for key process steps to ensure consistency and quality.
Establish comprehensive quality criteria and outgoing quality control (OQC) procedures at suppliers prior to shipment.
Monitor and analyze supplier yield data, production metrics, and quality performance to identify trends and drive corrective actions.
Lead and align our internal engineering teams (Design, Product, Reliability, Quality) - teams that do not report to you - to ensure supplier capabilities align with product requirements and committed timelines.
Conduct supplier technical audits and provide mentorship on standard processes in manufacturing and quality control.
Own issues end to end - drive the investigation to root cause and come to the table with a recommended solution, an implementation plan, and an owner, not only with a flagged problem.
Requirements:
What we need to see:
Bachelor's or Master's degree in Electrical Engineering, Mechanical Engineering, Materials Science, or a related technical field.
8+ years of proven experience in engineering roles, with a significant portion focused on process management, manufacturing engineering, or NPI.
Proven track record to understand complex manufacturing processes and identify critical control points.
Strong background in process quality methodologies. Experience with yield analysis, data interpretation, driving root cause analysis for technical issues and driving corrective actions through to verified closure.
Excellent communication, interpersonal, and leadership skills to effectively collaborate with internal teams and external suppliers.
Demonstrated ability to run a technical program to committed timelines and to influence and mobilize cross-functional teams over whom you have no direct authority.
Sound engineering and quality judgment weighed against the operational needs of the business - able to make and defend pragmatic trade-offs between technical risk, schedule, capacity, and cost.
Resilience and effectiveness under high workload and ambiguity in a dynamic environment.

Ways to stand out from the crowd:
Experience with advanced manufacturing technologies (e.g., advanced packaging, high-speed PCBs, Electro-Mechanical, mechanical, electrical, high Speed IO, etc.).
Familiarity with NPI processes in a fast-paced technology company.
Proven track record of driving significant quality or yield improvements at suppliers.
Experience with DFM (Design for Manufacturability) and DFT (Design for Testability) principles
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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עדכון קורות החיים לפני שליחה
8837110
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מודים לך שלקחת חלק בשיפור התוכן שלנו :)
3 ימים
Location: Yokne`am
Job Type: Full Time
Our New Product Introduction (NPI) team is growing, and we're looking for a highly motivated and diligent Engineering Vendor Manager to join us. In this critical role, you'll be responsible for the engineering management of our most strategic and technologically advanced suppliers, ensuring the highest quality and reliability of components for our groundbreaking products.

Our Networking division is a leading supplier of innovative end-to-end NVLINK, InfiniBand and Ethernet connectivity solutions and services for servers and storage. We offer market-leading solutions that include adapter cards, switches, cables, and software to support networking technologies. Our products optimize data center performance, using our AI solution and deliver industry-leading bandwidth and scalability. In addition, we serve a wide range of sectors, including high-performance computing, enterprise, data centers, cloud computing, big data, and Web 2.0.

What you'll be doing:
Lead engineering engagement with strategic and critical suppliers for new product introductions (NPI) and ongoing production, identify potential risks, critical parameters, and areas for optimization.
Define and implement clear monitoring and documentation requirements for key process steps to ensure consistency and quality.
Establish comprehensive quality criteria and outgoing quality control (OQC) procedures at suppliers prior to shipment.
Monitor and analyze supplier yield data, production metrics, and quality performance to identify trends and drive corrective actions.
Collaborate closely with internal engineering teams (Design, Product, Reliability, Quality) to ensure supplier capabilities align with product requirements.
Drive continuous improvement initiatives at suppliers to enhance process control, yield, and overall product quality.
Conduct supplier technical audits and provide mentorship on standard processes in manufacturing and quality control.
Act as the primary technical interface between us and strategic suppliers, resolving complex engineering challenges.
Requirements:
What we need to see:
Bachelor's or Master's degree in Electrical Engineering, Mechanical Engineering, Materials Science, or a related technical field.
8+ years of relevant experience.
proven experience in engineering roles, with a significant portion focused on supplier management, manufacturing engineering, or NP.
Proven track record to understand complex manufacturing processes and identify critical control points.
Strong background in quality methodologies (e.g., Six Sigma, FMEA, SPC). Experience with yield analysis, data interpretation, and driving root cause analysis for technical issues.
Excellent communication, interpersonal, and leadership skills to effectively collaborate with internal teams and external suppliers.
Ability to travel internationally to supplier sites as needed.

Ways to stand out from the crowd:
Experience with advanced manufacturing technologies (e.g., advanced packaging, high-speed PCBs, Electro-Mechanical, mechanical, electrical, high Speed IO, etc.).
Familiarity with NPI processes in a fast-paced technology company.
Proven track record of driving significant quality or yield improvements at suppliers.
Experience with DFM (Design for Manufacturability) and DFT (Design for Testability) principles.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8836188
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03/09/2026
חברה חסויה
Location: Caesarea
Job Type: Full Time
We are looking for a passionate and dynamic Mechanical Engineer, with a hands-on approach, to join our R&D team.

The role involves the research and development of robotic mechanisms incorporating motors, gears and sensors, from concept to mass production.



Responsibilities:

Design and develop complex robotic mechanisms and assemblies from concept through production.

Lead mechanical development activities across the full product lifecycle, including concept generation, detailed design, prototyping, drawing release, manufacturing support, integration and verification.

Define and execute test and validation methodologies to confirm design performance and compliance with engineering requirements.

Generate and maintain high-quality engineering documentation, including requirements, calculations, design reviews, protocols, reports, and change orders.

Collaborate closely with cross-functional stakeholders including systems engineering, software, electronics, manufacturing, quality, and operations.

Manage technical interactions with suppliers and support component sourcing, qualification, and manufacturability activities.
Requirements:
B.Sc. in Mechanical Engineering with at least 5+ years of experience in robotics/automation field.

Demonstrated experience in the design of robotic mechanisms incorporating motors, sensors, bearing systems, and high-precision components.

Experience in medical device development - advantage.

Strong proficiency in SolidWorks, including complex assemblies and detailed drawings.

Experience performing finite element analysis (FEA).

Experience working with PLM systems and ECO/ECN processes.

Familiarity with Design for Manufacturing (DFM) principles - advantage.

Strong technical problem-solving and analytical capabilities.

Ability to manage multiple priorities in a dynamic development environment.

Excellent communication and interpersonal skills.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8809278
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תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
חברה חסויה
Location: Caesarea
Job Type: Full Time
We're a global team of creative experts, bringing our unique backgrounds and bold ideas to push boundaries and help each other grow. Because full product development-from design to qualification to production-is within our team, were able to think differently, experiment more, and work quickly. Join us to power the future of the digital world.


YOUR IMPACT

Build, lead, and mentor a team of mechanical design engineers responsible for Engineering Validation Board (EVB) mechanical development.

Define team priorities, project plans, and resource allocation in collaboration with Hardware Program Managers and cross-functional engineering teams.

Lead the mechanical design of complex EVBs, including board-level mechanics, fixtures, thermal solutions, structural components, and lab infrastructure.

Drive Design for Manufacturing (DFM), Design for Assembly (DFA), and Design for Test (DFT) to ensure efficient prototype builds and engineering validation.

Develop innovative mechanical concepts to support aggressive product development schedules and multiple concurrent programs.

Partner closely with Electrical Engineering, PCB Layout, Signal Integrity (SI), Power Integrity (PI), Thermal Engineering, Packaging, and Contract Manufacturers throughout the product lifecycle.

Support prototype assembly, debugging, validation, and bring-up activities, ensuring rapid issue resolution.

Lead root cause investigations, failure analysis, and corrective actions for mechanical and assembly-related issues.

Perform design reviews, risk assessments, and implement mitigation plans to improve product quality, reliability, and execution.

Define and continuously improve mechanical design methodologies, engineering processes, and best practices for EVB development.

Work closely with external suppliers and contract manufacturers to ensure manufacturability, quality, cost optimization, and schedule execution.
Requirements:
B.Sc (https://B.Sc). in Mechanical Engineering (M.Sc. is an advantage).

8+ years of experience in mechanical design for electronic products.

4+ years of experience leading engineering teams in an R&D environment.

Proven experience designing electro-mechanical systems for complex electronic hardware.

Strong hands-on experience with 3D CAD tools (Creo preferred).

Experience designing for sheet metal, CNC machining, injection molding, and other manufacturing technologies.

Strong understanding of PCB/PCBA mechanical integration and mechanical tolerance analysis.

PREFERRED QUALIFICATIONS

Experience developing Engineering Validation Boards (EVBs) or complex networking/server hardware.

Knowledge of high-speed electronic systems and mechanical integration challenges.

Experience with thermal management solutions for high-power electronic assemblies.

Familiarity with laboratory fixtures, test hardware, and validation infrastructure.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8837087
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2 ימים
חברה חסויה
Location: Haifa
Job Type: Full Time
As an R&D Mechanical Engineer at Augury, you will own the design of new parts and assemblies, design parts for machining and injection molding, perform analytical calculations and V&V tests.

Youll work closely with mechanical, hardware, V&V, sustain, manufacturing, and external sub contractors, to deliver innovative, reliable, and scalable IoT devices.

A Day In Your Life
Design mechanical parts and mechanisms, for highly challenging environments, from initial concepts, through all design phases, until transfer to production.
Master 3D CAD models and drawings for mechanical components, assemblies, jigs, and fixtures (including release management and GD&T).
Design for plastics: mostly parts for injection molding, compression and other classical manufacturing methods.
Run prototype validation: mechanical inspection, stress testing, sealing, field testing and support high level system validation procedures.
Cooperate with multidisciplinary teams (HW, V&V, FW, Algo), utilizing analytical thinking and strong theoretical background.
Transfer parts for production, in collaboration with the engineering team, and following product lifecycle methodologies.
Work with subcontractors and vendors in Israel and internationally.
Requirements:
BSc Mechanical Engineering.
3-5 years of experience as a Mechanical engineer in R&D, with hands-on experience.
Experience in classic machine design: Parts, assemblies, and mechanisms.
Proven knowledge in manufacturing methods: Machining, injection molding, coatings, materials (aluminium, stainless steel, polymers), and geometric tolerances.
Familiarity with NPI processes, DFM, DFX, and transfer to production.
High proficiency in 3D CAD (Onshape, SolidWorks).
Ability to independently lead initiatives and navigate ambiguous environments with changing priorities.
Analytical thinking skills and a data-driven, structured engineering approach.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8837361
סגור
שירות זה פתוח ללקוחות VIP בלבד