דרושים » ניהול ביניים » Lead Supplier Quality Engineer

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לפני 11 שעות
חברה חסויה
Job Type: Full Time and Hybrid work
We are seeking a highly motivated and detail-oriented Supplier Quality Engineer to join our
Quality team to be responsible for ensuring supplier compliance with quality requirements,
driving continuous improvement initiatives, managing supplier performance, and supporting
IQC department.
Key responsibilities:
? Qualify, develop, and monitor suppliers to ensure compliance with company quality
standards.
? Conduct supplier audits (process, system, and product audits).
? Lead supplier corrective and preventive action (SCAR/CAPA) activities using structured
problem-solving methodologies.
? Analyze supplier quality performance using KPIs and implement improvement plans.
? Support supplier selection, qualification, and approval processes.
? Review and approve supplier documentation, including PPAP, FAI, control plans, PFMEA,
and process flow diagrams.
Requirements:
? Bachelors degree in engineering or a related technical field.
? Experience working with electronic, mechanical, or electromechanical products.
? Strong understanding of quality management systems and supplier quality processes.
? Experience conducting supplier audits and QBRs.
? Strong communication and interpersonal skills.
? Ability to manage multiple priorities and work independently.
? Proficiency in Microsoft Office applications.
? Fluent in English (written and spoken).
Preferred Qualifications
? Lead Auditor certification.
? CQE (Certified Quality Engineer) certification.
? Experience with ERP and PLM systems, priority- advantage.
? Experience in high-tech, aerospace, or semiconductor industries- advantage.
Required Skills Competencies
? Root Cause Analysis (5 Why, Fishbone, 8D)
? First Article Inspection (FAI)
? Corrective and Preventive Actions (CAPA)
This position is open to all candidates.
 
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12/06/2026
חברה חסויה
Location: Netanya
Job Type: Full Time
our company is an international Medical Device company that develops and manufactures innovative medical equipment. Specifically, we develop infusion pumps and their related accessory products. Job Description: supplier approval/disapproval including supplier maintenance and issuance of the Approved Supplier List. Leading the SCARS process including SCAR initiation, SCAR follow up, Supplier investigation approval including root cause analysis and SCAR closure. Leading the supplier audits process (including initial and surveillance audits) for critical suppliers, service centers, laboratories etc. by conducting on site / remote audits. Issuance and execution of the supplier audits plan including supplier audits follow up and supplier non-conformance follow up and response approval.
* Support the execution of service agreements, quality agreements with suppliers and service centers. Leading the supplier score card process, including trending.
* Serve as  CAPA Coordinator and Subject Matter Expert
* Responsible and accountable for CAPA ownership, timely execution, and effectiveness of CAPAs. This includes creation, collaboration with functional teams on Problem Statement writing/Scope identification/Risk Assessment/Containment/Correction/CAPA plans/Verification of local and global compliance to CAPA procedures to ensure timely effective closure of CAPAs Generate data and key quality trending information for use in periodic reviews like Quality Metric Reviews and Management Review for CAPA and supplier processes.
* Work within, and ensure adherence to Quality system procedures, work instructions and other Quality system requirements.
* Write, update, release, and sign quality documentation within the Quality management system
Direct manager: QA Compliance Manager
Requirements:
Education o Practical Engineer/ B.Sc. in Quality/ Biomedical/ Biotechnology or similar or CQM / CQE. Job skills:
* 3- 5 years of relevant experience.
* Good knowledge of ISO 9001, ISO 13485 and international standards. o Knowledge and experience with quality processes. o Experience in the field of Medical Devices - an advantage. o Knowledge and experience in quality processes o Auditor certificate - an advantage.
Computer skills: o Good knowledge of MS-Office tools (Excel, Word, PP). o Acquaintance with E-Document management systems. o Knowledge of statistical based computer programs such as Excel and/or Minitab
Language skills:
* English and Hebrew - fluent.
Personality:
* Ability to evaluate, prioritize, organize, multitask and problem solving.
* Ability to work in a team as well as independently
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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עדכון קורות החיים לפני שליחה
8691131
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05/07/2026
חברה חסויה
Location: Netanya
Job Type: Full Time
Job Description:

supplier approval/disapproval including supplier maintenance and issuance of the Approved Supplier List.

Leading the SCARS process including SCAR initiation, SCAR follow up, Supplier investigation approval including root cause analysis and SCAR closure.

Leading the supplier audits process (including initial and surveillance audits) for critical suppliers, service centers, laboratories etc. by conducting on site / remote audits. Issuance and execution of the supplier audits plan including supplier audits follow up and supplier non-conformance follow up and response approval.

Support the execution of service agreements, quality agreements with suppliers and service centers.

Leading the supplier score card process, including trending.

Serve as Eitan Medicals CAPA Coordinator and Subject Matter Expert
Responsible and accountable for CAPA ownership, timely execution, and effectiveness of CAPAs. This includes creation, collaboration with functional teams on Problem Statement writing/Scope identification/Risk Assessment/Containment/Correction/CAPA plans/Verification of local and global compliance to CAPA procedures to ensure timely effective closure of CAPAs.

Generate data and key quality trending information for use in periodic reviews like Quality Metric Reviews and Management Review for CAPA and supplier processes.

Work within, and ensure adherence to Quality System procedures, work instructions and other Quality System requirements.
Write, update, release, and sign quality documentation within the Quality management system.

Direct manager: QA Compliance Manager
Requirements:
Education:
Practical Engineer/ B.Sc. in Quality/ Biomedical/ Biotechnology or similar or CQM / CQE.

Job skills:
3-5 years of relevant experience.
Good knowledge of ISO 9001, ISO 13485 and international standards.
Knowledge and experience with quality processes.
Experience in the field of Medical Devices - an advantage.
Knowledge and experience in quality processes.
Auditor certificate - an advantage.

Computer skills:
Good knowledge of MS-Office tools (Excel, Word, PP).
Acquaintance with E-Document management systems.
Knowledge of statistical based computer programs such as Excel and/or Minitab.

Language skills:
English and Hebrew - fluent.

Personality:
Ability to evaluate, prioritize, organize, multitask and problem solving.
Ability to work in a team as well as independently
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8723940
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Location: Haifa
Job Type: Full Time
Required Team Lead Supplier Quality and Development Engineering
The Team Leader, Supplier Quality and Development role is a player/coach role with team leadership responsibilities and individual responsibilities to drive quality for assigned suppliers, including quality plan implementation.
You will be responsible for the Supplier Quality and Development activities within specified manufacturing sites and assigned supplier ownership. Youll have responsibilities as the site Point of Leadership, and accountable for coordinating supplier management efforts.
We are a leading global medical technology and digital solutions innovator. Our mission is to improve lives in moments that matter. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.
Job Description
Essential Responsibilities
Responsible for execution of QMS/compliance requirements associated with Supplier Management. This includes supplier qualifications, action plans, audits, performance monitoring, and assisting key suppliers towards industrial standards of excellence
SQD Point of leadership at Haifa and Rehovot sites, acting as the primary interface with Program Management, Production, Engineering, and Quality Assurance. Serve as Lead Auditee for internal and external audits related to the Purchasing Control procedure.
Responsible for people leadership activities including recruiting, performance management, people development, and technical development to deliver outcomes across their scope.
Utilizes in-depth knowledge of discipline and analytical thinking to execute policy/strategy. Basic knowledge of related job disciplines.
Actively support supports Value Creation Programs (VCP) in close collaboration with Engineering and Sourcing, ensuring quality improvements are aligned with cost optimization, productivity, and business objectives. Drive idea generation with suppliers on quality improvement that will drive cost optimization.
Requirements:
Bachelors degree in sciences, Engineering, Procurement, Supply Chain Management, or Finance.
Bachelors degree-level knowledge in Engineering/Quality/Supply Chain (or equivalent experience per country), plus advanced experience in Supplier Quality / Sourcing interface.
Proven understanding of Quality Systems / regulations and audit environment (e.g., ISO 13485 / equivalent medical QMS frameworks), plus analytical problem-solving and project execution skills.
Influence/communication - establishes good relationships; drives continuous improvement across functional boundaries with an SQDCI mindset.
Willing to travel domestically and internationally up to 30% of time.
Desired Characteristics
Masters degree in Business Administration.
Strong oral and written communication skills. Demonstrated ability to analyze and resolve problems. Ability to document, plan, market, and execute programs. Established project management skills.
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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חברה חסויה
Location: Yokne`am
Job Type: Full Time and English Speakers
we are looking for a NPI Quality Engineer.
Key Responsibilities:
Coordinate Cross-Functional Teams: Collaborate with R&D, design, procurement, and production teams to ensure smooth product launches.
Process Development: Develop and optimize manufacturing processes for new products using quality tools.
Documentation: Review and maintain process documentation, work instructions, and operator training materials.
Prototype Builds: Support PT builds and production ramp-up activities, ensuring product quality, yield, and cycle times meet expectations.
Issue Resolution: Identify and resolve production issues during development and transfer phases.
Compliance: Ensure compliance with quality and regulatory standards.
Continuous Improvement: Implement continuous improvement practices to enhance production efficiency and product quality.
Requirements:
Education:
CQE or B.sc in quality engineering.
Bachelors degree in mechanical, Electrical, Industrial Engineering, or a related field - advantage.
Minimum 3 years of experience in NPI or manufacturing engineering, with a focus on transferring products from development to production.
Knowledge of manufacturing processes and materials and familiarity with quality systems and regulatory requirements.
ability to manage multiple projects simultaneously.
Strong problem-solving and analytical abilities (8D /A3 method)
Interpersonal and communication skills.
Familiarity with ISO 9001 and /or AS9100.
Certified internal auditor - advantage
Complete Control of MS Office with advanced Excel Skills
ERP / PLM knowledge.
Fluent Hebrew and English (Reading, Writing and Speaking)
Preferred Qualifications:
Experience in industries such as electronics and mechanics and multidiscipline systems.
Knowledge of lean manufacturing principles, Six Sigma methodologies, and quality systems.
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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3 ימים
חברה חסויה
Location: Beit She'An
Job Type: Full Time
our company, a leading defense company developing and manufacturing life-saving radar systems, is seeking a student role within the Supplier Quality team. The position includes supporting Quality Assurance activities with suppliers in Israel and abroad, analyzing quality data, handling nonconformities, and supporting continuous improvement processes to ensure compliance with the companys quality requirements. Responsibilities
* Monitor supplier performance using quality metrics
* Handle nonconformance reports and quality deviations with suppliers
* Collect, analyze, and present quality data
* Maintain and update quality documents, procedures, and records in the companys systems
Requirements:
Requirements
* Undergraduate student in Mechanical Engineering, Electronics, Industrial Engineering and Management, or a relevant engineering field
* At least one year of studies remaining
* CQE studies during the degree program or CQE graduate - an advantage, not mandatory
* Availability to work at least 2-3 days per week
* Strong command of Office applications, especially Excel
* Good command of English
* Ability to work independently as well as part of a team Advantages
* Familiarity with quality standards such as ISO 9001 / AS9100
* Ability to read mechanical drawings and technical requirements
* Previous experience in manufacturing, quality, or engineering
* Experience working with ERP or PLM systems
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8735800
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05/07/2026
חברה חסויה
Location: Haifa
Job Type: Full Time
we are looking for a Product Quality Engineer.
Job Responsibilities:
Facilitates operations performance monitoring, reporting, improvement and development, facilitates improvement programs in factory, and supports analytical testing and Supplier Quality Engineering (SQE), Supplier Quality Assurance (SQA) and Purchasing.
Conducts assessment of impact to Process Failure Mode and Effects Analysis (PFMEA) and associated controls in relation to design changes and assists in Manufacturing Process Development and Design Transfer activities.
Leads analysis of defects for determining dispositions of non-conformances, drives management of Non-Conformances (NC) and Quality Notifications (QN) and facilitates implementation of effective Corrective and Preventive Actions (CAPA) actions.
Handles non conformance events and investigations in the factory and guides material review board activities for non-conformance disposition management.
Facilitates timely quality engineering and quality assurance tasks, ensures manufacturing quality systems are maintained, handles single or complex process validation and process improvement activities, and helps in completion of New Product Introduction (NPI) and product transfers in factory.
Possesses working knowledge of generic products/services and Quality Engineering and Continuous Improvement techniques, follows processes and operational policies in selecting methods for obtaining solutions, and frequently interacts with supervisors and functional peer groups to gain cooperation of others.
Acts as an advisor to subordinates to meet schedules and/or solve technical problems, develops and administers schedules and performance requirements, and may have budget responsibilities.
Cultivates effective relationships, demonstrating full understanding of area of specialization, demonstrates good working relationships with suppliers, and previous experience of participation in several New Product Introductions (NPIs).
Leads validation protocols, facilitates production builds to support validation activities, analyzes data for reports, process improvement initiatives, and validation activities.
Utilizes advanced statistical analysis methods to interpret complex data trends, resolve a wide range of moderate complexity requests, and provide strategic insights for continuous enhancement of quality standards and process efficiency.
Discusses detailed, strategic quality metrics and reports with stakeholders, highlighting significant achievements, emerging trends, and actionable insights to drive advanced improvement initiatives and ensure regulatory compliance.
Delivers specialized advanced training programs on cutting-edge quality standards, advanced methodologies, and best practices, fostering alignment across functions and advancing excellence in operational practices at an expert proficiency level.
Cultivates effective relationships with internal/external partners and provides influence over projects and peer groups, demonstrating full understanding of area of specialization.
Requirements:
Bachelor's / Master's Degree in Mechanical Engineering, Electronics Engineering, Science or equivalent.
Minimum required Experience:
Minimum 2 years of experience with Bachelor's in areas such as Quality Engineering, Safety Engineering, Process Engineering or equivalent OR no prior experience required with Master's Degree.
Previous experience from medical device companies- Must
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8723358
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7 ימים
חברה חסויה
Location: Beit She'An
Job Type: Full Time
DRS RADA Technologies , a leading defense company developing and manufacturing life-saving radar systems, is seeking an Complaints & RMA Engineer for its Beit She’an manufacturing facility. The Customer Complaints & RMA Engineer is responsible for the engineering aspects of customer complaints and Returned Material Authorization (RMA) processes. The role involves conducting failure Analysis, performing root cause analysis, leading corrective and preventive actions, and driving continuous improvement of product quality and reliability. The position requires close collaboration with cross-functional teams and customers worldwide to ensure professional, rapid, and effective resolution of quality issues. Responsibilities
* Conduct failure investigations for products returned through RMA processes and customer complaints.
* Analyze product failures using engineering tools and methodologies to identify root causes (Root Cause Analysis).
* Define and lead Corrective and Preventive Actions (CAPA) in collaboration with Engineering, Manufacturing, Quality, and Purchasing teams.
* Prepare detailed failure analysis reports, document findings, and present conclusions to relevant stakeholders.
* Provide engineering ownership of customer complaint investigations through to technical closure.
* Communicate with customers in Israel and internationally, presenting investigation results and providing technical recommendations.
* Support NCR, MRB, and quality investigation processes as required.
* Analyze recurring failure trends and lead initiatives to improve product quality and reliability.
* Coordinate with testing laboratories, suppliers, and subcontractors to perform testing and validate findings.
* Participate in internal and external quality audits as required.
* Ensure compliance with company procedures, quality standards, and applicable regulatory requirements.
Requirements:
* Minimum of 2–3 years of experience as a Quality Engineer, Product Engineer, Reliability Engineer, or in a similar role within a manufacturing environment.
* Bachelor’s degree in Electronics Engineering \ Electrical Engineering \ Mechanical Engineering \ Industrial Engineering \ Quality Engineering, or another relevant engineering discipline - required.
* Proven experience in Failure Analysis and Root Cause Analysis.
* Experience working with quality processes such as CAPA, NCR, MRB, and RMA.
* Familiarity with industry quality standards; experience in an AS9100 environment is an advantage.
* Experience working with cross-functional teams and customers in Israel and internationally.
* Experience with ERP systems and Quality Management Systems (QMS).
* Proficiency in Microsoft Excel and Microsoft Office applications.
* Excellent written and spoken English.
* Strong analytical skills, excellent organizational abilities, technical report writing skills, and the ability to drive cross-functional processes.
* Familiarity with electronic test equipment and the ability to read engineering drawings - an advantage.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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עדכון קורות החיים לפני שליחה
8730161
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18/06/2026
Location: Yokne`am
Job Type: Full Time
Join our outstanding team and contribute to our legacy of innovation in the Senior Product Quality and Reliability role! We are dedicated to pushing the boundaries of pioneering technology. The Senior Product Quality and Reliability Engineer will provide leadership and management for the Networking system product quality within the organization. Establish, maintain, and optimize an effective quality management methods and target to achieve high quality performance.

As part of our team, you will work on networking system products and ensure their readiness for high-volume manufacturing. Leading and mentoring root cause analysis for issues related to design, manufacturing or customers. Enhance and improve products performance by proactive risk assessment and other prevention methods. This is an outstanding opportunity to be part of a company that is crafting the future of AI and computing.



What youll be doing:

Own Product Quality and Reliability performance of Networking system products. Providing leadership expertise in product performance and quality.

Maintain and monitor product health thru structured routines and metrics, enable effective alert mechanism for early identification

Lead structured problem solving and risk assessment for quality issues originating from production and customer. Ensure product readiness for HVM manufacturing and scale

Responsible for customer quality issues and working within organization to resolve

Lead critical processes for product quality and performance e.g - CRB, PCN ; Non conforming material review - MRB

Drive continues improvement initiatives in design, verification and validation processes, manufacturing quality throughout the entire product life cycle and improvement plan.
Requirements:
What we need to see:

Graduate in Electrical engineering / Chemical / Mechanical Science, other technical degrees will be considered.

8+ years experience leading quality of multidisciplinary products (Electrical, Mechanical, Process)

Proficient with Product lifecycle management and QMS processes

Strong written and verbal communication, ability to interact at all management levels

Strong organizational and project management skills , proven matrix management experience in high paced ​ dynamic environment

Experience facilitating complex problem solving​



Ways to stand out from the crowd:

Experience from process oriented electronic manufacturing industry along with top data center customers

Familiar with NVlink and Ethernet products and protocols

Experience in System integration and/or HW board design manufacturing

Strong problem-solving skills and analytical ability.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8701242
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14/06/2026
Location: Netanya
Job Type: Full Time
DRS RADA is a global pioneer of radar systems for active military protection, counter-drone applications, critical infrastructure protection, and border surveillance. We are looking for an experienced QMS and Regulatory Compliance Director to join our team. Job Description: Overall responsibility for managing, maintaining, and continuously improving the organization’s Quality Management System (QMS), including certification processes, internal and external audits, regulatory activities, and compliance oversight, while ensuring alignment with organizational objectives, applicable standards, procedures, customer requirements, and relevant compliance obligations. Key Responsibilities:
* Lead and manage the organization’s Quality Management System (QMS) end-to-end across development, project management, operations, and production.
* Ensure the establishment, implementation, maintenance, and continuous improvement of quality processes, procedures, and controls in alignment with applicable standards and organizational requirements.
* Manage and develop the quality and regulatory team, providing professional leadership across quality, regulatory, and compliance activities.
* Oversee certification activities, internal and external audits, and the effective management of nonconformities, corrective actions, and preventive actions.
* Lead regulatory and compliance activities to ensure adherence to applicable requirements, customer expectations, and organizational commitments.
* Monitor performance through quality metrics and management reporting, and drive a culture of quality, accountability, and continuous improvement across the organization.
Requirements:
* Experience in managing Quality Management Systems (QMS).
* In-depth knowledge of AS9100 and ISO 9001 standards.
* Previous managerial experience.
* Relevant academic degree.
* Experience in compliance and regulatory activities.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8692781
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02/07/2026
Location: Haifa
Job Type: Full Time
we are seeking a Systems Applications Engineer to serve as a key technical resource for equipment readiness, system bring-up, and ongoing product support. In this role, you will partner closely with NPI Program Management, Engineering, suppliers, and cross-functional teams to support bills of material, evaluate design and assembly changes, ensure system and subsystem test coverage, and drive resolution of equipment issues. You will become a technical expert in prober operation and bring-up, helping ensure timely response, effective troubleshooting, and field validation of corrective actions.



Partner with NPI Program Management to understand, manage, and assess bills of material for current and future equipment configurations.
Evaluate BOM changes, design documentation, assembly requirements, and related technical updates to support product readiness and manufacturability.
Review system and subsystem test coverage to help ensure required tests exist, are properly executed, and support product quality expectations.
Work closely with Teradyne Engineering and external suppliers to troubleshoot current tool failures, identify root cause, and drive corrective action.
Support implementation of corrective actions and ensure appropriate field validation is completed.
Develop deep technical expertise in prober operation, system bring-up, and equipment behavior.
Serve as a first line of technical response for prober issues, ensuring timely escalation, clear communication, and effective remedies.
Collaborate across engineering, operations, suppliers, and field teams to improve equipment performance, reliability, and supportability.
Requirements:
Bachelors degree in Engineering or a related technical discipline, or equivalent practical experience.
10+ years experience supporting complex equipment, systems engineering, applications engineering, NPI, manufacturing, or field support environments.
Working knowledge of bills of material, engineering change processes, design documentation, assembly requirements, and test validation.
Strong troubleshooting and analytical skills, including root cause analysis and corrective action follow-through.
Ability to work effectively with Engineering, Program Management, suppliers, and field teams to resolve technical issues.
Hands-on experience with equipment bring-up, system/subsystem testing, or prober operation is strongly preferred.
Strong communication skills with the ability to explain technical issues clearly and drive alignment across teams.
Detail-oriented, proactive, and comfortable operating in a fast-paced technical environment.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8721458
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