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1 ימים
חברה חסויה
Location: Tel Aviv-Yafo
Job Type: Full Time
We are looking for Quality Manager with a 5 years experience.
This position will be responsible for overseeing the quality within the company, focusing on the development, implementation, and monitoring of quality methodologies and processes.
The role will be hands-on, including internal quality control, supplier audits, development of quality documentation, and management of multidisciplinary processes within the company.
The Quality Manager will work closely with our development & engineers, production, and regulatory teams to ensure compliance with rigorous quality standards.
Key Responsibilities:
Developing Quality Methodology: Develop and implement comprehensive quality methodologies, focusing on multi-disciplinary products (including hardware, electronics, mmechanics and software).
Hands-on Role: Perform independent quality control, design, and manage continuous quality improvement processes.
USO Certification and Quality Control: Ensure compliance with international quality certifications and standards, such as ISO, and specific defense standards (e.g., MIL-STD).
Supplier Audits: Conduct quality audits for suppliers in the hardware and electronics domains, analyze results, and provide recommendations for improvement.
Organizing Proposals and Processes: Define processes for organizing proposals and ensure quality requirements are met during supplier engagement.
Quality Documentation: Create and update technical documents, quality reports, specifications, and standard operating procedures.
Collaboration with Development and Production Teams: Coordinate with development, engineering, production, and regulatory teams to ensure compliance with quality standards.
Failure investigations, PFMEA management, MRB committees, and more.
Requirements:
Education: Bachelors degree in Electronics Engineering, Industrial Engineering, Systems Engineering, or a relevant engineering field.
Professional Experience: At least 5 years of experience in a similar role, particularly in companies developing multi-disciplinary products (hardware, software, and electronics).
Experience in a multidisciplinary manufacturing company Must
Experience in defense Sector in a similar job- Must.
Experience working with strict quality standards and certifications, including defense-specific standards such as MIL-STD, AS9100, or similar.
Quality Certifications: Certifications in quality management (ISO 9001) are a plus.
Project Management Skills: Ability to manage quality-related projects, organize processes, and handle technological challenges.
Technological Skills: Experience with quality management systems, ERP and tools related to hardware and electronics.
Personal Skills: Analytical thinking, problem-solving abilities, ability to work under pressure, and excellent communication skills with internal teams and suppliers.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8218659
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משרות דומות שיכולות לעניין אותך
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משרה בלעדית
2 ימים
קבוצת נישה
דרושים בקבוצת נישה
Job Type: Full Time and English Speakers
Join a leading Medical Device Company as a Director of Quality to be responsible for leading the Quality Management system in compliance with ISO 13485, 21 CFR Part 820, MDSAP and other applicable regulatory requirements. This role oversees quality across the product lifecycle, including design control, operations, and post-market activities.
Key Responsibilities:
Lead implementation and oversight of design control processes for new and modified devices.
Manage and ensure quality in operations: production, final product release, incoming inspection activities, process validation and supplier quality.
Manage configuration and doc control process.
Own and maintain the quality management system, including internal audits, CAPA, complaints, and management review.
Prepare for and lead external audits (e.g. notified bodies, FDA).
Requirements:
Bachelors degree in engineering, life sciences, or a related field (Masters preferred).
Minimum 10 years of experience in quality roles within the medical device industry.
Strong knowledge of ISO 13485, 21 CFR Part 820, and MDSAP requirements.
Proven leadership and team management experience.
Experience with quality in Operations.
Experience with internal/external audits and regulatory inspections. Certified lead auditor.
Experience in design control process.
Excellent problem-solving, communication, and cross-functional collaboration skills.
Fluent in English Hebrew
This position is open to all candidates.
 
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הגשת מועמדות
עדכון קורות החיים לפני שליחה
8182328
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מודים לך שלקחת חלק בשיפור התוכן שלנו :)
1 ימים
חברה חסויה
Location: Tel Aviv-Yafo
Job Type: Full Time
A world-leading material science company, focused on the research, development, manufacturing, and marketing of vision and light control technologies that support safe, sustainable, comfortable, and agile user experiences across various industries.
We are seeking an experienced Quality Assurance Manager to lead our quality initiatives and ensure compliance with global standards. This role is integral to maintaining our high manufacturing standards, driving continuous improvement, and collaborating with cross-functional teams to enhance product quality and performance.
Joining means becoming part of a cutting-edge, fast-growing company that values innovation, excellence, and teamwork in shaping the future of smart materials.

Please send a copy of your CV in English.
Responsibilities
Drive quality performance and continuous improvement across the organization.
Develop and implement product quality assurance strategies across all development phases.
Define QA compliance objectives and ensure adherence to international standards (ISO 9001, VDA 6.3, IATF 16949).
Establish quality control methods, documentation, and risk management practices (FMEA, APQP, PPAP, SPC, MSA).
Investigate root causes of deviations with R&D and production teams, ensuring corrective actions.
Oversee supplier evaluations, internal audits, and customer compliance audits.
Train and supervise technical staff in quality processes, testing, and reporting.
Serve as the product safety representative and liaise with global quality teams.
Prepare for and manage internal, customer, and certification audits.
Willingness to travel internationally when required.
Requirements:
Minimum of 5 years of quality assurance experience in production processes within a manufacturing company
Experience in implementing and managing quality assurance metrics
Familiarity with ISO 9001:2015 regulations, automotive industry standards (IATF 16949, VDA 6.3), CAPA, and automotive core tools (e.g., FMEA, APQP, PPAP, SPC, MSA)
Excellent problem-solving, interpersonal communication, and project management skills (8D, Ishikawa, 5W)
Ability to lead cross-functional organizational processes
Certified 1st and 2nd party auditor for IATF 16949; VDA 6.3 auditor certification preferred
Strong technical skills
Proficiency in Microsoft Office tools, particularly Excel
High proficiency in written and spoken English
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8219067
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דיווח על תוכן לא הולם או מפלה
מה השם שלך?
תיאור
שליחה
סגור
v נשלח
תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
Location: Tel Aviv-Yafo
Job Type: Full Time
a fast-growing medical technology company transforming the fields of hematology and cell morphology analysis. As a team, we work to enable faster, earlier detection and diagnosis of blood-related diseases, so patients can start treatment sooner and have better outcomes. We are collaborative and global and every individual at is part of a life-saving mission.
About the job
We are looking for a Quality Assurance Compliance Specialist to join our compliance and RA team, which plays a central role in both pre-market and post-market activities. The team is responsible for regulatory activities, quality management system, and ensuring compliance with applicable standards, including those related to privacy.

The Quality Assurance Compliance Specialist will play an important role in the companys regulatory, quality and compliance activities, such as ensuring compliance with relevant quality standards (including ISO 13485:2016, 21 CFR 820, MDSAP and IVDR); supporting internal audits, corrective efforts and different quality projects; and defining quality procedures, protocols and tools.

What youll be doing
Provide ongoing support for the companys quality management activities, including SDLC, PMS, product investigation, operations, training management, supplier management, and document control
Maintain the companys quality management system (QMS)
Evaluate and address quality assessment related to customer complaints
Prepare and maintain technical documentation in compliance with standards such as ISO 13485, 21 CFR 820, and IVDR
Collaborate with cross-functional teams, including R&D, product development, and technical support on quality-related activities
Perform privacy-related tasks, such as evaluating suppliers for privacy compliance and reviewing data processing agreements (DPAs)
Analyze post-market surveillance data to support company initiatives
Prepare teams for internal and external audits
Requirements:
Bachelor's degree in industrial engineering, biotechnology engineering, life science/exact science, or law
At least 5 years of experience working with the QMS of a medical device company, including development, implementation, or compliance with standards such as ISO 13485 and FDA regulations
Understanding of QA processes and methodologies (ISO 13485:2016, 21 CFR 820 or similar)
Understanding of privacy requirements such as HIPAA, GDPR and ISO27799
Ability to collaborate effectively with cross-functional teams to achieve quality objectives
A motivated, collaborative, and proactive approach to work
Team orientation
Excellent communication skills (both written and verbal)
Strong attention to detail
Ability to lead and implement processes
English proficiency
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8170674
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סגור
דיווח על תוכן לא הולם או מפלה
מה השם שלך?
תיאור
שליחה
סגור
v נשלח
תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
25/05/2025
חברה חסויה
Location: Tel Aviv-Yafo
Job Type: Full Time
Gauzy (NASDAQ: GAUZ) is a world-leading material science company, focused on the research, development, manufacturing, and marketing of vision and light control technologies that support safe, sustainable, comfortable, and agile user experiences across various industries. We are seeking an experienced Quality Assurance Manager to lead our quality initiatives and ensure compliance with global standards. This role is integral to maintaining our high manufacturing standards, driving continuous improvement, and collaborating with cross-functional teams to enhance product quality and performance. Joining Gauzy means becoming part of a cutting-edge, fast-growing company that values innovation, excellence, and teamwork in shaping the future of smart materials. *** Please send a copy of your CV in English.

Responsibilities:

* Drive quality performance and continuous improvement across the organization.
* Develop and implement product quality assurance strategies across all development phases.
* Define QA compliance objectives and ensure adherence to international standards (ISO 9001, VDA 6.3, IATF 16949).
* Establish quality control methods, documentation, and risk management practices (FMEA, APQP, PPAP, SPC, MSA).
* Investigate root causes of deviations with R&D and production teams, ensuring corrective actions.
* Oversee supplier evaluations, internal audits, and customer compliance audits.
* Train and supervise technical staff in quality processes, testing, and reporting.
* Serve as the product safety representative and liaise with global quality teams.
* Prepare for and manage internal, customer, and certification audits.
* Willingness to travel internationally when required.
Requirements:
* Minimum of 5 years of quality assurance experience in production processes within a manufacturing company
* Experience in implementing and managing quality assurance metrics
* Familiarity with ISO 9001:2015 regulations, automotive industry standards (IATF 16949, VDA 6.3), CAPA, and automotive core tools (e.g., FMEA, APQP, PPAP, SPC, MSA)
* Excellent problem-solving, interpersonal communication, and project management skills (8D, Ishikawa, 5W)
* Ability to lead cross-functional organizational processes
* Certified 1st and 2nd party auditor for IATF 16949; VDA 6.3 auditor certification preferred
* Strong technical skills
* Proficiency in Microsoft Office tools, particularly Excel
* High proficiency in written and spoken English **This position is hybrid: 4 days from the office and 1 day from home**
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8092785
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סגור
דיווח על תוכן לא הולם או מפלה
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סגור
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תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
חברה חסויה
Location: Tel Aviv-Yafo
Job Type: Full Time
We are seeking a highly motivated and experienced Production and Quality Engineer to join our dynamic team. This is a critical, cross-functional role focused on ensuring the sustained and scalable production of our innovative device, while maintaining the highest standards of product quality, process readiness, and production continuity.
As a Production and Quality Engineer, you will be instrumental in bridging the gap between design and manufacturing, owning key engineering tasks across mechanical, electrical, and system-level components. This includes vital responsibilities such as Bill of Materials (BOM) validation, robust test system support, and seamless interface with our contract manufacturers (CMs). You will also play a pivotal role in supporting crucial New Product Introduction (NPI) activities.
Key Responsibilities:
Production Engineering:
Maintain and update the production tree (BOM structure) for the device and all associated hardware and accessories.
Proactively ensure that all products can be manufactured with a minimum of two approved BOM alternatives, strategically mitigating single-point-of-failure risks.
Define, develop, and provide comprehensive support for production test systems, fixtures, and calibration protocols, while continuously improving production costs and efficiency.
Develop clear and precise production instructions to support manufacturing across all production sites.
Act as the primary interface with production partners, implementing manufacturing best practices and swiftly resolving production-related issues.
Quality Engineering:
Lead investigations and resolve production and field quality issues through rigorous root cause analysis and the implementation of effective corrective action plans (CAPAs).
Define, implement, and continuously monitor quality control protocols, test methods, and inspection guidelines to uphold product excellence.
Maintain traceability and comprehensive documentation for all production and Quality Assurance (QA) processes.
Engineering & Change Management:
Lead the efficient execution of Engineering Change Orders (ECOs) and maintain precise SKU/version management for all products.
Coordinate seamlessly with engineering, logistics, and suppliers to ensure the effective and timely rollout of all changes.
Provide essential support for the launch and configuration of accessory SKUs and bundles as required.
Production Risk Mitigation:
Proactively identify and address risks associated with single-source components, tools, materials, and other critical aspects of the production process.
Work collaboratively to define and qualify alternative components and production paths to ensure continuity.
Plan and manage the tooling roadmap to strategically support future production scalability.
Cross-Functional Support:
Collaborate closely with hardware engineering, supply chain, and logistics teams to ensure optimal production alignment and efficiency.
Provide robust support for internal and external operations projects.
Requirements:
5+ years of hands-on experience in production engineering, quality engineering.
Strong, proven understanding of Bill of Materials (BOMs), Engineering Change Orders (ECOs), production test processes, and successful collaboration with Contract Manufacturers (CMs).
Familiarity with established quality systems (e.g., ISO 9001, ISO 13485) and proficient in failure analysis techniques.
Demonstrated ability to manage complex cross-functional technical projects and communicate clearly and effectively with diverse stakeholders.
Fluent in English, with excellent organizational and meticulous documentation skills.
"Startup-ready" mindset: Comfortable working independently, managing multiple priorities, and thriving across disciplines in a fast-paced, dynamic environment.
Familiarity with medical 510K Class I or II - An advantage.
Hands-on experience with test fixtures, calibration tools, and factory bring-up - An advantage.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8200145
סגור
שירות זה פתוח ללקוחות VIP בלבד
סגור
דיווח על תוכן לא הולם או מפלה
מה השם שלך?
תיאור
שליחה
סגור
v נשלח
תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
חברה חסויה
Location: Tel Aviv-Yafo
Job Type: Full Time
a fast-growing medical technology company transforming the fields of hematology and cell morphology analysis. As a team, we work to enable faster, earlier detection and diagnosis of blood-related diseases, so patients can start treatment sooner and have better outcomes. We are collaborative and global and every individual at is part of a life-saving mission.

About the job
We are looking for a compliance analyst to join our compliance and RA team, which plays a central role in both pre-market and post-market activities. The team is responsible for regulatory activities, quality management system, and ensuring compliance with applicable standards, including those related to privacy.

The analyst will play an important role in the companys regulatory, quality and compliance activities, such as ensuring compliance with relevant quality standards (including ISO 13485:2016, 21 CFR 820, MDSAP and IVDR); supporting internal audits, corrective efforts and different quality projects; and defining quality procedures, protocols and tools.

What youll be doing
Provide ongoing support for the companys quality management activities, including SDLC, PMS, product investigation, operations, training management, supplier management, and document control
Maintain the companys quality management system (QMS)
Evaluate and address quality assessment related to customer complaints
Prepare and maintain technical documentation in compliance with standards such as ISO 13485, 21 CFR 820, and IVDR
Collaborate with cross-functional teams, including R&D, product development, and technical support on quality-related activities
Perform privacy-related tasks, such as evaluating suppliers for privacy compliance and reviewing data processing agreements (DPAs)
Analyze post-market surveillance data to support company initiatives
Prepare teams for internal and external audits
Requirements:
Bachelor's degree in industrial engineering, biotechnology engineering, life science/exact science, or law
At least three years of experience working with the QMS of a medical device company, including development, implementation, or compliance with standards such as ISO 13485 and FDA regulations
Understanding of QA processes and methodologies (ISO 13485:2016, 21 CFR 820 or similar)
Understanding of privacy requirements such as HIPAA, GDPR and ISO27799
Ability to collaborate effectively with cross-functional teams to achieve quality objectives
A motivated, collaborative, and proactive approach to work
Team orientation
Excellent communication skills (both written and verbal)
Strong attention to detail
Ability to lead and implement processes
English proficiency
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8170342
סגור
שירות זה פתוח ללקוחות VIP בלבד
סגור
דיווח על תוכן לא הולם או מפלה
מה השם שלך?
תיאור
שליחה
סגור
v נשלח
תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
29/05/2025
חברה חסויה
Location: Tel Aviv-Yafo
Job Type: Full Time
we are the global leader in control systems for quantum computing, providing the hardware and software tools researchers and businesses need to build quantum computers from the ground up. We are assembling the strongest team of professionals in the world with the goal of revolutionizing how quantum computers are built and controlled while accelerating their arrival. Come join a multi-disciplinary, world-class team and work on a new class of problems at the cutting edge of technology, science, and business.
We are seeking a highly skilled Senior Board Design Engineer to join our Product Engineering Team. In this role, you will be responsible for designing and debugging test boards used in the validation and production of our hardware products. You will work closely with cross-functional teams to ensure high-quality test infrastructure and support the production process by analyzing failures and implementing corrective actions.
Key Responsibilities:
Design and develop digital and mixed-signal test boards, including schematic design, layout, and validation.
Debug complex digital boards with components such as microcontrollers, CPUs, and FPGAs.
Develop and test FPGA-based solutions for test and measurement applications.
Work closely with mechanical and software engineers to integrate test systems.
Support production yield improvement, failure analysis, and corrective actions implementation.
Collaborate with manufacturing and quality teams to ensure seamless production processes.
Create documentation, test procedures, and design reviews to support product lifecycle management.
Requirements:
Bachelor's degree in Electronics Engineering, Electrical Engineering, or a related field.
5-6 years of experience in hardware development, focusing on board design.
Hands-on experience with failure analysis and debug techniques of digital and mixed signals boards.
Hands-on experience with FPGA development and programming.
Proficiency in schematic and PCB layout design.
Preferred Qualifications:
Technical leadership experience
Knowledge of electronic board production flows and manufacturing best practices.
Experience with Python scripting for hardware automation and testing.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8199126
סגור
שירות זה פתוח ללקוחות VIP בלבד
סגור
דיווח על תוכן לא הולם או מפלה
מה השם שלך?
תיאור
שליחה
סגור
v נשלח
תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
01/06/2025
חברה חסויה
Location: Tel Aviv-Yafo
Job Type: Full Time
we are the global leader in control systems for quantum computing, providing the hardware and software tools researchers and businesses need to build quantum computers from the ground up. We are pushing the envelope in a field on the verge of exponential growth, bringing about opportunities like those made possible with the invention of classical computing 50 years ago. We are assembling the strongest team of professionals in the world with the goal of revolutionizing how quantum computers are built and controlled while accelerating their arrival. Come join a multi-disciplinary, world-class team and work on a new class of problems at the cutting edge of technology, science, and business.
We are seeking a skilled Board Design Engineer to join our Product Engineering Team. In this role, you will be responsible for designing and debugging test boards used in the validation and production of our hardware products. You will work closely with cross-functional teams to ensure high-quality test infrastructure and support the production process by analyzing failures and implementing corrective actions.
Join us in this exciting journey to redefine the future of quantum computing.
Key Responsibilities:
Design and develop digital and mixed-signal test boards, including schematic design, layout, and validation.
Debug complex digital boards with components such as microcontrollers, CPUs, and FPGAs.
Develop and test FPGA-based solutions for test and measurement applications.
Work closely with mechanical and software engineers to integrate test systems.
Support production yield improvement, failure analysis, and corrective actions implementation.
Collaborate with manufacturing and quality teams to ensure seamless production processes.
Create documentation, test procedures, and design reviews to support product lifecycle management.
Requirements:
Bachelor's degree in Electronics Engineering, Electrical Engineering, or a related field.
1-2 years of experience in hardware development, focusing on board design.
Hands-on experience with HW bring-up, integration and debug techniques of digital and mixed signals boards.
Proficiency in schematic and PCB layout design.
Preferred Qualifications:
Hands-on experience with FPGA development and programming.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8200009
סגור
שירות זה פתוח ללקוחות VIP בלבד
סגור
דיווח על תוכן לא הולם או מפלה
מה השם שלך?
תיאור
שליחה
סגור
v נשלח
תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
29/05/2025
חברה חסויה
Location: Tel Aviv-Yafo
Job Type: Full Time
we are a global leader in control systems for quantum computing, a field on the verge of exponential growth. Our innovative hardware and software mark a groundbreaking approach in quantum computer control, scaling from individual qubits to expansive arrays of thousands.
At the core of our company's lies a passionate and ambitious team committed to reshaping the construction and operation of quantum computers. Our work is fueled by a deep understanding of customer needs, driving us to deliver unparalleled solutions in this revolutionary field.
The hardware development team spans two global sites one in Tel Aviv and one in Copenhagen. The two teams work seamlessly together across projects, and we try to foster an open dialogue to foster creativity and commitment. The hardware team is responsible for all hardware within our company's spanning from room-temperature control hardware to our cryogenic QPU carriers.
We are looking for a seasoned Electronics Engineer with over 5 years of hands-on experience in analog circuit design and power supply engineering. In this role, you will focus on developing and refining analog circuitssuch as amplifiers, filters, and DACs operating from DC to 2GHzand power supply solutions across various topologies. As the go-to person in electronics, youll work as a key contributor and technical expert, collaborating closely with our hardware teams in Denmark and Israel, as well as operations during the NPI phase.
Key Responsibilities
Analog Circuit Development:
Design and optimize analog circuitry, including amplifiers, filters, and signal generation modules (DACs) covering frequencies from DC up to 2GHz and above.
Power Supply Engineering:
Develop robust power supply designs across various schemes (buck/boost converters, LDOs, switching regulators, etc.) that meet high-performance standards.
Simulation & Design:
Utilize Altium for PCB design and LTspice for circuit simulation to validate and refine your designs.
Design for Manufacturing & Test (DFM/DFT):
Incorporate DFM and DFT best practices to ensure reliability, manufacturability, and scalability across many channels in compact form factors.
Performance & Compliance:
Ensure designs meet stringent low-noise requirements and EMI/EMC compliance for high-performance applications.
Cross-Functional Collaboration:
Work closely with hardware teams in both Denmark and Israel, and engage with operations during the NPI process to ensure seamless integration of your designs.
Technical Expertise:
Act as the electronics subject matter expert within the team, providing technical sparring and review to peers.
Requirements:
Experience: 5+ years in analog circuit and power electronics design.
Technical Proficiency:
Extensive experience in designing amplifiers, filters, signal generation circuits, and DACs for high-frequency applications (DC-2GHz).
Proven track record in developing complex power supply systems (e.g., buck/boost converters, LDOs, switching regulators).
Tools:
Proficient in Altium and LTspice.
DFM/DFT Knowledge:
Deep understanding of design for manufacturability and testability to support robust, scalable production.
Industry Exposure:
Experience with telecom, radar, aerospace, or similar high-performance sectors is a plus.
Education:
B.Sc. or higher degree in Electrical Engineering or a related field.
Personal Attributes
Technical Authority: Recognized as the go-to person for electronics, with the ability to mentor and collaborate with peers.
Detail-Oriented: Meticulous approach to ensuring low-noise designs and EMI/EMC compliance while scaling to many channels in a small form factor.
Collaborative: Strong communication skills and a proven ability to work effectively with global teams, including remote coordination and occasional travel.
Innovative & Proactive: Eager to push boundaries and refine designs in fast-paced, high-performance environments.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8199224
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חברה חסויה
Location: Tel Aviv-Yafo
Job Type: Full Time and Travel Required
Were looking for a Process Improvement Engineer to bring fresh thinking and strategic focus to our Supply Chain Operation team. In this key role, you'll lead efforts to uncover inefficiencies, streamline operations, and deliver meaningful improvements across the business. This opportunity will have a direct impact on how fast we can grow and scale our operations to meet customer demand. You will wear multiple hats and be required to learn and master multiple areas of the business to deliver measurable improvements in key metrics and business outcomes.
This is a great opportunity to be part of one of the fastest-growing AI infrastructure companies in history, an organization that is in the center of the hurricane being created by the revolution in artificial intelligence.
Responsibilities:
Create and maintain process documentation, including flowcharts, standard operating procedures, and training materials
Analyze existing business processes and identify areas for improvement and optimization
Lead idea generation for innovative design/process solutions to existing operational problems
Develop and implement process improvement strategies that align with organizational goals
Conduct regular process audits and performance measurements to ensure continuous improvement
Champion continuous improvement initiatives across all Operations functions (Manufacturing, Quality, Service Logistics, Quote to Cash, Planning, Supply Base, etc.) ensuring cross-functional engagement and end to end process alignment
Up to 15% regional and WW travel depending on location and business needs.
Requirements:
Qualifications:
Bachelor's degree in engineering, mechanical, operations, supply chain, business administration, or equivalent STEM field
Minimum 5 years experience in supply chain operations, manufacturing or engineering role with demonstrated focus in process improvement.
Technical Skills:
Experience in Lean Management, Six Sigma and other operations engineer tools
Knowledge of manufacturing processes and quality control methods
Familiarity with relevant industry standards and regulations
Ability to translate complex technical concepts into easy-to-understand language for non-technical stakeholders
Soft Skills:
Excellent communication and interpersonal skills
Strong problem-solving and analytical skills
Ability to work independently and as part of a team in a fast-paced environment
Project management and stakeholder engagement
Strong organizational and time management 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
8200026
סגור
שירות זה פתוח ללקוחות VIP בלבד