דרושים » חשמל ואלקטרוניקה » Sr. Production and Suppliers Quality Engineer (QA Specialist)

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לפני 10 שעות
Location: Merkaz
We are seeking a highly motivated and experienced Sr. Production and Quality Engineer to drive exceptional product quality, patient safety, and field reliability across the Installed Base (IB). This is a key technical role supporting production stability, RMA/DOA investigations, Automated Test Equipment (ATE) performance, and cross-functional quality engineering initiatives in a regulated medical device environment
Key Responsibilities
In this role, you will
Support RMA/DOA processes and continuous reduction of field failures.
Support qualifications and control of ATE testers in production lines.
Support ECO/ECR processes, NPI projects, product updates, and cross-functional engineering changes.
Work closely with R&D, engineering, manufacturing, and operations teams to enhance product quality and resolve technical issues.
Drive continuous improvement initiatives using tools such as Six Sigma, Lean, and Root Cause Analysis (RCA).
Participate in supplier selection and conduct suppliers audits.
Ensure compliance with ISO 13485, FDA 21 CFR 820, MDR, and other applicable medical device regulations.
Maintain and support quality documentation, including CAPA, Non-Conformance Reports (NCRs), and risk management documentation.
Requirements:
Bachelors degree in Engineering (Mechanical, Electrical, Biomedical, or related field).
7+ years of experience in quality in medical device company
Strong analytical and problem-solving skills, including hands-on experience with RCA tools (5-Why, Fishbone, etc.).
Familiarity with ATE systems, V&V and process validations, production testing, and/or field reliability analysis - a strong advantage
Lead auditor of ISO13485, FDA 21 CFR 820, and ISO 14971 risk management.
Excellent communication and collaboration skills, with the ability to work effectively across functions.
A proactive, structured, and detail-oriented working style.
Fluent in English
This position is open to all candidates.
 
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29/04/2026
חברה חסויה
Location: Kiryat Gat
Job Type: Full Time
We are seeking a Quality Engineer to ensure product and process quality across manufacturing, suppliers, and new product introduction activities. The role supports and maintains the Quality Management System, ensures compliance with applicable standards, and implements effective quality controls throughout the product lifecycle. The Quality Engineer leads root cause analysis and corrective actions, works closely with cross-functional teams, and drives continuous improvement to enhance quality performance and customer satisfaction.
Key Responsibilities:
Support and maintain the Quality Management System (QMS) in compliance with ISO 9001 and applicable standards
Lead investigations of nonconformances, deviations, and customer issues, including root cause analysis and CAPA
Define and support inspection plans, acceptance criteria, and quality controls across manufacturing
Participate in New Product Introduction (NPI) activities, including design reviews, FMEA, pilot builds, and FAI
Support supplier quality activities, including issue resolution, corrective actions, and performance monitoring
Conduct and support internal and supplier audits and ensure timely closure of findings
Analyze quality data and KPIs to identify trends and drive continuous improvement initiatives
Collaborate with Engineering, Operations, Supply Chain, and other stakeholders to ensure quality objectives are met
Requirements:
Bachelors degree in Engineering (Mechanical, Industrial, Manufacturing, Electrical, or related)
3+ years of experience in Quality Engineering or Manufacturing Quality
Working knowledge of QMS and ISO 9001 (or equivalent)
Experience conducting or supporting internal and/or supplier audits
Hands-on experience with nonconformances, root cause analysis, and CAPA
Familiarity with SPC/AQL and manufacturing environments
Experience supporting NPI activities (FMEA, pilot builds, FAI)
Fluent Hebrew and English (written and spoken)
Preferred Requirements:
Quality or Continuous Improvement certifications (CQE, Six Sigma)
Experience in regulated industries (ISO 13485, AS9100, FDA)
Experience with supplier quality management, including global suppliers
Proficiency with quality tools, data analysis, and ERP/PLM systems
Ability to lead cross-functional initiatives and influence without authority
This position is open to all candidates.
 
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חברה חסויה
Location: Haifa
Job Type: Full Time
We are seeking a proactive and detail-oriented AI Regulatory Engineer to ensure that AI-based clinical features for ultrasound systems comply with evolving global regulatory requirements-particularly FDA regulations for AI-enabled medical devices.
This role is critical as AI has become a highly regulated domain, requiring specialized regulatory strategies, risk management approaches, and lifecycle governance. The AI Regulatory Engineer will work closely with AI engineering, clinical, quality, product management, and regulatory affairs teams to define and execute the correct AI regulatory and submission strategy across the full product lifecycle.
Job Description
Key Responsibilities
AI Regulatory Strategy & Compliance
Interpret and apply regulatory frameworks and guidance for AI-enabled medical devices, including FDA, EU MDR/IVDR, and global regulations.
Define and drive AI regulatory strategies for clinical ultrasound features, including SaMD and AI-enabled device functions.
Design and execute clinical validation strategy and plans for AI-driven ultrasound products in compliance with regulatory standards.
Support FDA submission pathways (e.g., 510(k), De Novo, PMA) for AI-based features, including AI-specific regulatory positioning.
Risk Management & Safety for AI:
Lead AI-focused risk management activities in accordance with ISO 14971, addressing AI-specific hazards such as bias, robustness, generalization risk, and clinical misuse.
Perform and maintain AI-specific risk analyses (e.g., AI FMEA, algorithm hazard analysis, clinical performance risk).
Ensure traceability between clinical requirements, AI behavior, risk controls, and verification/validation evidence.
Regulatory Documentation & Submissions:
Prepare and maintain AI-related regulatory documentation, including:
AI descriptions and intended use statements
Training and validation dataset descriptions
Performance evaluation and clinical evidence summaries
Algorithm change management and lifecycle documentation
Support creation of FDA-ready AI documentation, including transparency, explainability, and human-factors considerations.
AI Lifecycle & Change Management:
Define regulatory-compliant AI lifecycle strategies, including updates, retraining, and change impact assessment.
Support implementation of Predetermined Change Control Plans (PCCP) or equivalent AI lifecycle strategies.
Ensure alignment between AI development practices and regulatory expectations for locked vs. adaptive algorithms.
Cross-Functional Collaboration:
Collaborate closely with:
AI engineers and data scientists
Clinical and medical affairs teams
Quality, systems, and V&V engineers
Product management and regulatory affairs
Embed regulatory and safety requirements early into AI design, data strategy, and clinical validation plans.
Regulatory Intelligence & Audits:
Monitor evolving AI regulations, FDA guidance, standards, and industry best practices.
Communicate regulatory changes and their impact on AI roadmaps and product strategy.
Support internal audits, design reviews, and external regulatory inspections related to AI and clinical safety.
Provide training and guidance on AI regulatory and safety topics to engineering and product teams.
דרישות:
Bachelors or Masters degree in Engineering, Computer Science, Biomedical Engineering, or related field.
Experience working in regulated medical device environments, preferably involving AI-driven clinical features.
Solid understanding of medical device regulatory frameworks, with emphasis on FDA and EU MDR.
Experience with risk management methodologies and safety processes for medical devices.
Strong analytical, documentation, and communication skills.
Ability to work independently and collaboratively in a multidisciplinary environment.
Preferred Qualifications:
Experience with AI-enabled medical devices, SaMD, or clinical decision support systems.
Familiarity with FDA guidance on AI in medical devices, Good AI Pr המשרה מיועדת לנשים ולגברים כאחד.
 
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06/05/2026
חברה חסויה
Location: Ramat Gan
Job Type: Full Time
This role offers an exciting opportunity to contribute to the development of innovative delivery systems and support clinical investigations and complaint handling, partnering with QA and Clinical Development that will revolutionize the treatment of cardiovascular diseases.

How you will make an impact: 

As an R&D Engineer, Provides expertise in the optimization of product development for the Innovalve delivery system and accessories.

Design and Development: Design, analyze, and develop components and processes that meet stringent quality, performance, and regulatory requirements.

Problem-Solving: Identify and troubleshoot complex technical issues that arise during development and clinical trials.

Custom Solutions: Develop tailored solutions for unique design challenges and clinical requirements

Lead and perform product investigations for returned products and complaint samples, including hands-on functional evaluation, data collection and custom testing setup development.

Analyze investigation data to determine probable root cause and contributing factors using structured problem-solving methods (e.g., 5-Why, Fishbone).

Prepare clear technical summary reports and present investigation results to cross-functional teams; track actions to closure.

Work closely with Quality Assurance to support complaint handling workflows, ensure investigation documentation is complete, and align on conclusions and next steps.

Follow up on complaints arising from clinical cases (e.g., case questions, device performance observations) and provide timely technical input to R&D, QA and Clinical Development teams.

Collaborate with cross-functional partners to define and implement corrective actions addressing issues identified through investigations.

Support change management activities (e.g., ECOs) and contribute to risk management updates as needed based on investigation learnings.

Clinical procedure experience - Advantage.
Requirements:
B.Sc. in Mechanical engineering or Bio-medical engineering.

Minimum of 5 years of experience in relevant field.

Strong understanding of mechanical engineering principles, including materials science, stress analysis, and manufacturing processes.

Analytical, problem-solving, and critical thinking skills.

High verbal communication skills.

Great attention to detail and organizational skills.

Proficiency in English and Hebrew.

knowledge in CAD software (SolidWorks, or similar).

Experience with regulatory requirements (e.g., ISO 13485, FDA QSR).

Experience with medical devices development and quality documentation.

Travel abroad 25% of the time.

Ability to work independently and as part of a cross-functional team.
This position is open to all candidates.
 
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חברה חסויה
Location: Haifa
Job Type: Full Time
Required Senior System Engineer
Job Description Summary
As a Senior System Engineer, you will play a critical role in the design, development, integration, and verification of complex medical imaging systems. You will be responsible for translating clinical needs into technical requirements, ensuring the robust performance, safety, and regulatory compliance of our innovative healthcare solutions.
Job Description
Job Responsibilities
Lead and participate in the full product lifecycle, from concept and requirements definition through design, development, testing, and deployment of medical imaging systems.
Translate high-level clinical and user requirements into detailed system and subsystem specifications, ensuring traceability and comprehensive coverage.
Perform complex system analysis, modeling, and simulation to optimize system performance, identify potential risks, and propose innovative solutions.
Collaborate closely with cross-functional teams including hardware, software, clinical, quality assurance, regulatory, and manufacturing engineers to ensure seamless integration and successful product delivery.
Define and execute system verification and validation plans, including test protocols, data analysis, and reporting, to ensure compliance with medical device regulations (e.g., FDA, CE).
Conduct root cause analysis for system-level issues, propose effective corrective actions, and drive their implementation.
Contribute to the continuous improvement of system engineering processes, tools, and methodologies within the organization.
Mentor junior engineers and provide technical guidance on complex system engineering challenges.
Stay abreast of industry trends, emerging technologies, and regulatory changes relevant to medical imaging systems.
Requirements:
Bachelor's or Master's degree in Electrical Engineering, Biomedical Engineering, or a related technical field.
5+ years of experience in system engineering, with a significant portion in the medical device industry (preferably imaging systems such as MRI, CT, X-ray, Ultrasound).
Proven experience in defining system requirements, architecture, and design for complex products.
Strong understanding of medical device regulations (e.g., IEC 60601, ISO 13485, FDA QSR, MDR).
Experience with risk management activities for medical devices.
Excellent analytical, problem-solving, and decision-making skills.
Strong communication and interpersonal skills, with the ability to effectively collaborate with diverse teams.
Ability to work independently and as part of a team in a fast-paced, dynamic environment.
Fluency in English and Hebrew (written and spoken) is required.
This position is open to all candidates.
 
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חברה חסויה
Location: Haifa
Job Type: Full Time
Required Advanced Manufacturing Engineer
Job Description
Role Summary
The Advanced Manufacturing Engineer (AME) is responsible for industrializing and sustaining complex PET and SPECT imaging products at a high‑complexity electromechanical manufacturing site. The AME ensures robust manufacturability of high‑level mechanical assemblies, electronics integration, wiring, detector modules, motion systems, and system‑level testing. The role drives process development, tooling, validation, DFM/DFA, quality improvement, and readiness for production and NPIs.
NPI Leadership for PET & SPECT Imaging Systems
Lead manufacturing readiness for new PET/SPECT products, including process layout, tooling development, and new equipment introduction.
Participate in design reviews and influence DFM/DFA/DFT across mechanical assemblies, detector modules, power systems, wiring harnesses, and electromechanical subsystems.
Translate design intent into controlled, stable manufacturing processes.
Coordinate ECO implementation and ensure smooth manufacturing release.
Assembly Process Development & Optimization
Develop robust assembly processes for mechanical and electronic integration, alignment, torque control, and detector installation.
Define and design manufacturing jigs, tools, fixtures, and lifting/handling solutions required for large subsystems.
Lead design/manufacture of equipment, tooling, and jigs internally or via suppliers to eliminate defects.
Drive LEAN manufacturing implementation and support continuous improvement.
Conduct PFMEA for existing and new processes.
Quality & Problem Solving
Drive product quality improvements by identifying manufacturing issues and implementing cost‑effective solutions.
Work with Production Associates to resolve manufacturing and quality problems.
Oversee corrective action implementation in production or suppliers.
Support RCA through structured failure analysis.
System Integration & Testing Support
Support integration/testing of assembled PET/SPECT systems including calibration, alignment, motion validation, detector gain calibration, and safety checks.
Work with System Engineering to define test protocols and acceptance criteria.
Troubleshoot system issues related to electromechanical assemblies.
Validation & Regulatory Compliance
Own IQ/OQ/PQ for equipment, tools, and manufacturing processes.
Ensure compliance with ISO 13485, ISO 14971, 21 CFR 820, IEC 60601, and internal QMS requirements.
Maintain strong documentation practices including control plans, validation protocols, and DHR/DMR accuracy.
Ensure traceability for critical parameters, torques, and calibration data.
Supplier & Cross‑Functional CollaborationCollaborate with suppliers of mechanical assemblies, detector modules, wiring harnesses, and PCBs.
Lead technical discussions with suppliers for tooling, process capability, and quality issues.
Train and qualify production and supplier teams on processes and inspection/assembly methods.
EHS & Plant Compliance
Lead and support Environment, Health & Safety efforts aligned with site goals.
Ensure safe handling of large assemblies, HV systems, and radiation‑related components.
דרישות:
Drive product quality improvements through systematic problem solving.
Lead design requirements for manufacturing processes, tools, and fixtures.
Design and manufacture jigs, fixtures, and tooling (internal or supplier‑managed).
Strong experience with LEAN manufacturing and PFMEA execution.
Ability to resolve complex manufacturing and quality issues.
Leadership of NPI activities including tool development and equipment introduction.
ECO coordination and controlled release management.
Strong understanding of compliance, EHS, and regulated manufacturing.
Ability to train and qualify production and supplier teams.
Mechanical/electromechanical assembly expertise.
Experience with HV/LV wiring, detector systems, and motion integration.
Strong המשרה מיועדת לנשים ולגברים כאחד.
 
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20/04/2026
Location: Yokne'Am Illit
Job Type: Full Time
We are looking for NPI/Sustain Mechanical Engineer! Job description: The NPI/Sustain Mechanical Engineer is responsible for supporting new product introduction (NPI) from design through production, ensuring manufacturability, quality, and cost targets are met. The role includes sustaining engineering activities such as troubleshooting field issues, implementing design improvements, and supporting continuous product optimization. The engineer works cross-functionally with R&D, manufacturing, quality, and suppliers to resolve technical challenges and drive product readiness. Develop and maintain documentation, including drawings, TEST protocols, and validation reports.
Responsibilities:
Collaborate with the design engineering team to review and improve mechanical designs for manufacturability and cost-effectiveness.
Support the development of prototypes and testing of new designs. Plan, design, and perform prototype builds, including tests for functionality, durability, and reliability.
Ensure product designs are optimized for manufacturing.
Support production lines across multiple contract manufacturers, implement design improvements, and drive continuous product optimization.
Work with suppliers and manufacturers to ensure they understand the design and meet required specifications.
Identify and resolve mechanical design issues and challenges during the transition from prototype to production.
Prepare and maintain comprehensive product documentation, including technical drawings for tools, specifications and manufacturing instructions.
Conduct process validation IQ, OQ, and PQ activities to ensure that all systems and processes meet regulatory standards and deliver products of the highest quality.
Requirements:
Required Experience:
3-5 years of experience in new product introduction, product development, or manufacturing engineering, preferably in the medical device industry.
Hands-on experience with SolidWorks for mechanical design.
Familiarity with product lifecycle management (PLM) tools and processes.
Strong understanding of materials, manufacturing processes, and product testing methodologies.
Proficiency in root cause analysis and solving complex mechanical problems.
Excellent communication skills, both written and verbal.
Ability to work effectively in cross-functional teams and manage multiple projects simultaneously.
This position is open to all candidates.
 
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11/05/2026
חברה חסויה
Location: Netanya
Job Type: Full Time
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
Requirements:
Requirements: Education: B.Sc. in Biomedical/Biotechnology/Chemical Engineering Job skills:
* 2 -5 years of experience in QA /RA, in a medical device or pharma manufacturing company Deep knowledge in working according to Medical device regulations and GMP (FDA QSR 820, ISO 13485) Auditor qualification - an advantage Computer skills: Proficiency in Office products - Must. ERP systems, an advantage. Language skills: Fluent English - Mother tongue level Personality: Team player,Excellent interpersonal relations, Highly organized and detail oriented, Motivated and committed,Creative and proactive. Assertive with the ability to effectively lead and drive cross-functional collaboration; capable of confidently interacting with multiple departments, assigning tasks, and ensuring timely execution.
This position is open to all candidates.
 
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7 ימים
חברה חסויה
Location: Netanya
Job Type: Full Time
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
Requirements:
Education: B.Sc. in Biomedical\Biotechnology\Chemical Engineering
Job skills:
2 -5 years of experience in QA/RA, in a medical device or pharma manufacturing company
Deep knowledge in working according to Medical device regulations and GMP (FDA QSR 820, ISO 13485)
Auditor qualification - an advantage
Computer skills: Proficiency in Office products - Must. ERP systems, an advantage.
Language skills: Fluent English - Mother tongue level
Personality:
Team player ,Excellent interpersonal relations, Highly organized and detail oriented, Motivated and committed ,Creative and proactive.
Assertive with the ability to effectively lead and drive cross-functional collaboration; capable of confidently interacting with multiple departments, assigning tasks, and ensuring timely execution.
This position is open to all candidates.
 
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Location: Rehovot
Job Type: Full Time
Required Senior Process & Yield Engineer - Manufacturing
Position Overview
The Senior Process & Yield Engineer will play a key role in developing, optimizing, and sustaining manufacturing processes to ensure quality, device performance, and line yield.
This role involves deep technical ownership of process modules, cross functional problem solving, yield excursion management, and continuous improvement of factory performance.
The ideal candidate possesses hands on process expertise, strong data driven decision making capabilities, and a proven ability to lead complex engineering initiatives in a high volume manufacturing environment.
Job Description
Key Responsibilities
Sustaining Process Engineering:
Monitor process health and equipment performance; respond to line abnormalities and excursions in real time.
Collaborate with Equipment Engineering to ensure tool matching, qualification, and tool health stability.
Maintain process documentation, change management, FMEA, and risk assessments.
Process Development & Optimization:
Develop, characterize, and optimize process steps to meet device performance, yield, and cost targets.
Own and coach DOE planning and execution to improve process stability, robustness, and manufacturability.
Define process recipes, operating windows (EWAs), and control plans aligned with technology requirements.
Yield Engineering & Data Analysis:
Conduct root‑cause analysis for yield loss and parametric drift; drive corrective and preventive actions (CAPA).
Use statistical tools (JMP, Python, SPC systems) for yield trend analysis and early detection of process anomalies.
Lead continuous improvement cycles through Six Sigma and structured problem‑solving methodologies.
Cross-Functional Collaboration:
Work closely with device engineering, equipment teams, integration, and quality to resolve technical issues.
Support NPI (New Product Introduction) activities including process readiness, qualification, and ramp to volume.
Participate in cross-site technical forums, best-practice sharing, and global engineering programs.
Requirements:
B.Sc. in Materials Engineering, Chemical Engineering, Electrical Engineering, Physics, or related field.
5+ years of experience in manufacturing (process, integration, or yield engineering).
Strong statistical analysis abilities and familiarity with SPC, DOE, FDC, and yield management systems.
Experience with at least one major process module (e.g., Lithography, Etch, Diffusion, CMP, PVD/CVD, Implant, Wet Process, Metrology).
Demonstrated ability to solve complex technical problems systematically and drive closure.
Excellent communication skills and ability to work in fast-paced, cross-functional environments.
Way to stand out of the crowd:
Experience with advanced nodes, MEMS, SiPh, power devices, or specialty processes.
Knowledge of automation systems (MES, APC) and advanced data‑science tools (Python, SQL, ML-based detection).
Project management experience (Agile, Waterfall ).
Certifications such as Six Sigma Green Belt/Black Belt.
Leadership experience-mentoring junior engineers, leading projects, or multi-disciplinary task forces.
Personal Attributes:
Analytical mindset with strong attention to detail.
High sense of ownership and accountability.
Able to balance tactical firefighting with long‑term strategic improvements.
Collaborative, adaptable, and comfortable with ambiguity.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8629925
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חברה חסויה
Location: Ra'anana
Job Type: Full Time
We are seeking a highly skilled and motivated Electrical Validation (EV) Team and System Testing / ATE Team Leader to join our team. This position is crucial in supporting the design, development, and implementation of Automated Test Equipment (ATE) and production test systems.
The Electrical Validation team Lead manages the electrical validation function across our company hardware platforms. This role owns the validation strategy, methodology, lab infrastructure, and execution across all high-speed and control interfaces. The manager ensures robust electrical performance from early prototypes through production release and drives cross-functional alignment between design, SI, firmware, and manufacturing.
The role involves close collaboration with the HW R&D team, Quality, DevOps, and Contract Manufacturing (CM) teams to ensure the delivery of high-quality, reliable products.
This group is part of the HW R&D group.
Key Responsibilities
Define the electrical validation strategy for our company hardware platforms.
Own validation methodology for: High-speed Ethernet (100M-1600G), PCIe Gen1 to Gen5+, SerDes architectures (NRZ/PAM4), Control and management buses (I2C, SPI, RS-232, MDIO, etc.)
Establish structured validation plans aligned with hardware release milestones.
Build and manage a high-performance validation team.
Define lab architecture, including: Equipment selection (oscilloscopes, BERTs, analyzers), Compliance platforms, Automation frameworks, Signal integrity validation environments
Drive early engagement with board design and SI teams to ensure design-for-validation.
Oversee: Compliance (IEEE, PCI-SIG, OIF), Interoperability testing, Stress and margin testing
Lead root cause analysis of electrical failures and systemic issues.
Support NPI, manufacturing bring-up, and yield improvement.
Develop automation and scalable validation methodologies.
Define validation documentation standards and sign-off criteria.
Collaborate with system architecture and software teams to ensure HW-SW integration robustness.
Manage external labs and certification processes where required.
Drive continuous improvement of validation coverage and efficiency.
Lead the full ATE development lifecycle from requirements definition to execution in production, including GUI design and Python scripting.
Develop and maintain boundary scan applications using JTAG Technologies.
Define and maintain test fixtures, including JIGs/Bed-of-Nails, etc., in collaboration with mechanical vendors.
Implement full test traceability systems for production yield and stability monitoring.
Collaborate with R&D and Quality teams to drive product quality and reliability improvements.
Provide onsite support at CM sites, including station setup, installation, training, maintenance, and debugging.
Perform in-depth failure analysis and troubleshooting at the system and component level.
Utilize and maintain a range of test equipment, including:
Work with various communication protocols: TCP/IP, Telnet, SSH, HTTP, SNMP, SFTP, SCP, FTP, RS232, GPIB, I2C, and NI-VISA.
Support testing of embedded systems running on Linux platforms.
Requirements:
B.Sc. or M.Sc. in Electrical Engineering.
10+ years of experience in high-speed hardware validation in networking, telecom, or data center infrastructure.
3+ years of team leadership experience (preferred).
Deep expertise in: Ethernet PHY validation (IEEE 802.3), PCIe validation and compliance, High-speed SerDes characterization, Low-speed protocol validation (I2C, SPI, UART, MDIO)
Strong understanding of signal integrity and power integrity.
Hands-on experience with high-end lab equipment and compliance tools.
Experience defining and scaling validation infrastructure.
Proven ability to lead cross-functional debug efforts.
Experience with system-level architectures in distributed networking systems - strong advantage.
Strong project management and milestone-driven execution.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8647476
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שירות זה פתוח ללקוחות VIP בלבד