דרושים » אבטחת איכות QA » Production and Suppliers Quality Engineer Leader

משרות על המפה
 
בדיקת קורות חיים
VIP
הפוך ללקוח VIP
רגע, משהו חסר!
נשאר לך להשלים רק עוד פרט אחד:
 
שירות זה פתוח ללקוחות VIP בלבד
AllJObs VIP
כל החברות >
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 :)
לפני 21 שעות
Location: Merkaz
Job Type: Full Time
We are seeking a highly motivated and detail-oriented Production and Supplier Quality Team Leader .
This role is responsible for ensuring the
highest quality standards in production and supplier-provided components, driving continuous improvement, and maintaining compliance with
medical industry regulations.
In this role, you will
Lead and manage the Production & Supplier Quality team.
Develop and implement quality control processes for materials and products.
Collaborate with suppliers on quality agreements, audits, and corrective actions.
Oversee incoming inspections and ensure compliance with ISO 13485, FDA, MDR.
Drive continuous improvement using Six Sigma, Lean, RCA.
Conduct internal/external audits and manage CAPA, NCR, and risk documentation.
Mentor team members and foster a culture of quality excellence.
Requirements:
Bachelors in engineering or quality management.
10+ years in QA within medical device/high-tech manufacturing corporates.
Strong regulatory knowledge (ISO 13485, FDA).
Certifications: CQE, Six Sigma, Lead Auditor.
Leadership, analytical, and problem-solving skills.
This position is open to all candidates.
 
Hide
הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8505815
סגור
שירות זה פתוח ללקוחות VIP בלבד
משרות דומות שיכולות לעניין אותך
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 :)
לפני 55 דקות
דרושים בת.א.ג. כלים רפואיים בע"מ
Job Type: Full Time
1. Quality system Compliance: Ensure compliance with global regulatory requirements and standards for medical devices, including FDA QSR, ISO 13485, EU MDR, and others as applicable.
2. Design Control Risk Management: Participate in design control activities, ensuring quality considerations are integrated into product development processes. Lead risk management activities (FMEA, risk analysis) to identify and mitigate potential issues.
3. Process Validation and Verification: Oversee the validation and verification of design and manufacturing processes. Ensure robust testing methodologies are applied to prove that designs meet all requirements and regulations.
4. Documentation and Records: Write and maintain comprehensive documentation that meets regulatory and company requirements throughout the product development lifecycle. Ensure traceability and accessibility of quality records
Requirements:
Bachelor's degree in Engineering, Quality Assurance, or related field.
Minimum of 3-5 years of experience in quality engineering within the medical device industry.
Solid understanding of medical device regulations (FDA QSR, ISO 13485, EU MDR).
Experience with design control, risk management, and process validation principles.
Strong analytical, problem-solving, and project management skills.
Excellent communication and teamwork abilities.
Certification as a Quality Engineer (CQE) or similar is preferred.
? Personal Attributes:
Detail-oriented with a commitment to excellence.
Proactive in identifying issues and developing innovative solutions.
Ability to thrive in a fast-paced, collaborative environment.
Passionate about improving patient care through quality excellence.
This position is open to all candidates.
 
Show more...
הגשת מועמדות
עדכון קורות החיים לפני שליחה
8424772
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 :)
לפני 18 שעות
Location: Yokne'Am Illit
Job Type: Full Time
As a Quality Engineer in Manufacturing, you will play a key role in ensuring that products are manufactured in compliance with internal quality standards, regulatory requirements, and our companys commitment to patient safety and product excellence. This position partners closely with Manufacturing, Operations, R&D, and Supply Chain to drive quality improvements and support continuous improvement initiatives on the production floor.
Responsibilities may include the following and other duties may be assigned:
Provide quality engineering support for manufacturing operations and engineering.
Support production, engineering, validation activities including training, reviewing and approving documentation, work instructions, SOPs , supporting risk assessments, to ensure compliance with regulatory and quality system requirements.
Lead and support investigations of nonconformances, deviations, and CAPAs, including root cause analysis and implementation of corrective and preventive actions.
Collaborate with cross-functional teams to identify, assess, and mitigate quality risks in manufacturing processes.
Support internal and external audits, including preparation, participation, and follow-up on audit findings.
Drive continuous improvement initiatives using quality and lean methodologies.
Ensure effective implementation and monitoring of process controls and quality metrics.
Support change management activities ensuring requirements are identified and executed when applicable.
Participate in Management Review and Quality Metrics reporting.
Requirements:
Bachelors degree in Engineering, Biotechnology, Life Sciences, or a related field.
Minimum of 7 years of experience in quality engineering or quality assurance of production in medical devices or pharmaceuticals.
Knowledge of quality systems and regulatory requirements (e.g., ISO 13485, FDA QMSR, MDR).
Strong analytical and problem-solving skills.
Ability to work effectively in a cross-functional, fast-paced manufacturing environment.
Hands-on experience with ECOs, nonconformance management, CAPA, and root cause analysis tools.
Familiarity with statistical tools and data analysis.
Experience supporting audits and inspections.
Knowledge of Lean, Six Sigma, or continuous improvement methodologies- advantage.
Strong communication skills in English, both written and verbal.
This position is open to all candidates.
 
Show more...
הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8506287
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 :)
18/12/2025
חברה חסויה
Location: Yokne'Am Illit
Job Type: Full Time
we are a fast-growing medical device company focused on developing, manufacturing, and selling innovative devices for endovascular interventional procedures. Were looking for a QA Engineer to support and strengthen our manufacturing quality. In this role, youll work closely with cross-functional teams, execute day-to-day quality activities on the manufacturing floor and help drive continuous improvement in a hands-on, fast-paced environment.
LOCATION: Yokneam, Israel.
SCOPE & RESPONSIBILITIES
* Manage ECOs: conduct risk assessments, update relevant DMR documents and carry out necessary IQ, OQ, PQ activities if required, finalization of implementation tasks.
* Manage DCOs in the PLM system : Write and update QA procedures to ensure compliance with quality standards and regulatory requirements.
* Manage NCR and CAPA processes: Lead, write and supervise the NCR and CAPA processes, ensuring timely and effective resolutions.
* Manage QA production activities: Provide quality support to production operations, addressing deviations and non-conformities to maintain high product quality.
* Ensure Timely Resolution of Quality Issues: Promptly address all identified or assigned quality issues to prevent delays and maintain efficient operations.
* Participate in audits: Take part in internal and external audits, such as FDA inspections and notified body audits based on ISO13485, EUMDR, and MDSAP requirements.
* Manage Supplier quality: Manage supplier qualification and performance monitoring, including SCAR management, and support supplier audits.
Requirements:
Bachelor of Science degree or Engineering. 3-5 years of experience in medical device QA (ISO 13485, MDSAP, FDA QSR 820). Internal auditor certification- an advantage Ability to work in dynamic and multi-interfaced surroundings, micro and macro vision. Strong attention to details and Self-learning ability. Ability to manage time and priorities and work under pressure. English - high level (both written and spoken). Excellent leadership and people management skills. Service oriented. Kno wledge and practical experience in Priority An advantage.
This position is open to all candidates.
 
Show more...
הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8463448
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 :)
Location: Yokne`am
Job Type: Full Time and English Speakers
we are looking for a Quality Engineer (Root Cause Analysis).
The Quality Engineer is responsible for investigating and resolving quality-related issues, with a primary focus on Root Cause Analysis (RCA) and managing customer complaints. This role ensures that corrective and preventive actions are implemented effectively to maintain product quality and customer satisfaction.
Job Responsibilities:
Lead Root Cause Analysis for internal and external quality issues using structured problem-solving methodologies (e.g., 8D, Fishbone, 5 Whys).
Manage and resolve customer complaints, ensuring timely communication and resolution.
Develop and implement Corrective and Preventive Actions (CAPA) to prevent recurrence of issues.
Collaborate with cross-functional teams (Manufacturing, R&D, Supply Chain) to drive quality improvements.
Maintain documentation of investigations, actions, and results in compliance with company and regulatory standards.
Monitor quality metrics and trends to identify systemic issues and improvement opportunities.
Support audits and regulatory inspections related to quality processes.
Provide training and guidance on RCA tools and techniques to internal teams
Requirements:
Bachelors degree in Engineering or related field.
3+ years of experience in Quality Engineering or similar role.
Strong knowledge of RCA methodologies and quality tools (8D, 5Y, FMEA, SPC).
Experience in working directly with international customers.
Basic technical background in electronics and mechanics including technical understanding of drawings and procedures.
Experience in manufacturing or high-tech industry.
Excellent analytical and problem-solving skills.
Effective communication skills for customer interaction and internal collaboration.
Familiarity with ISO standards and regulatory requirements.
High-level proficiency in English.
Preferred Knowledge of statistical analysis and data-driven decision-making.
Preferred Proficiency in quality management systems (QMS).
This position is open to all candidates.
 
Show more...
הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8467614
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: Petah Tikva
Job Type: Full Time
'we are responsible to foster quality and excellence in our company's products and processes across the entire company. our company team focuses on ensuring high customers' satisfaction through continuous improvement and implementation of automotive standards and best-practices such as ASPICE, IATF16949, ISO 9001, VDA/AIAG Core Tools and ISO26262, both internal and across the entire supply chain. In order to support our company objectives, The QMS & Production Quality team is looking for a Production Quality Engineer
What will your job look like:
Define and implement production quality framework and workplan for our company's systems' NPI and serial production activities (from scratch)
Work closely with colleagues from other departments (PMs, development engineers, production engineers, management) and other organizations (suppliers and customers).
Work with contract manufacturers to analyze the production process, process capability, process capacity and measurement systems capability.
Assess and control the activities through performing VDA6.3 audits
Lead/Support 8D multi-disciplinary teams to investigate faults and failures
Lead and update PPAP folders for our company's systems
Identify opportunities for improvement and execute them.
Create relevant work items templates and coach the teams how to use them.
Assess KPIs of processes and activities and suggest corrective actions and improvement.
Represent production quality related issues with customers, suppliers and 3rd party organizations.
Requirements:
At least 5 years hands-on experience in quality of NPI and production processes in multidisciplinary systems' design & production companies (Automotive industry - significant advantage)
Knowledge in automotive core tools, standards and best practices - significant advantage
Certification and experience as supplier auditor per ISO19001 (VDA6.3 certification - significant advantage)
Experience in working with information systems - PLM, ALM, Jira (Working with Agile PLM & Polarion ALM - an advantage)
Highly organized, "Can-do" approach, Process-oriented, able to manage and follow-up on many tasks in parallel.
Able to work in a matrix organization while interfacing with diverse technical stakeholders.
Excellent communication skills in English (both verbal and written)
Able and willing to travel abroad
Bachelors degree - advantage.
This position is open to all candidates.
 
Show more...
הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8454251
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 :)
30/12/2025
חברה חסויה
Location: Tel Aviv-Yafo
Job Type: Full Time
we are a global leader in hybrid control systems for quantum computing, a field on the verge of exponential growth. Our innovative hardware and software offer a groundbreaking approach to controlling quantum computers, scaling from individual qubits to arrays of thousands. At the heart of our company is a passionate, ambitious team committed to transforming the construction and operation of quantum computers. Our deep understanding of customer needs drives us to deliver unmatched solutions in this revolutionary field.
We are seeking a Quality Engineer to join our growing operations department. In this role, you will be a champion of excellence, combining a true passion for quality work with a strong discipline for following and improving procedures. You will play a key role in ensuring our products consistently meet the highest standards of reliability and performance, helping us deliver safe, robust, and high-quality solutions to our customers.
Responsibilities:
Serve as a focal point for hardware quality topics with R&D (EE/ME), Operations, Supply Chain, and manufacturing partners.
Monitor production quality performance (yields, defects, scrap, rework) and ensure timely corrective actions in collaboration with R&D / manufacturing partners.
Monitor field quality performance (OOTB experience/RMAs), driving root cause analysis and corrective action implementation for critical hardware issues using structured quality tools (8D, 5 Whys, Pareto, etc.).
Implement, maintain, and improve hardware quality processes across the product lifecycle, ensuring effective adherence to ISO 9001 and relevant hardware/safety standards (CE, EMC, FCC, UL/IEC, WEEE, RoHS, etc.).
Conduct audits at manufacturing lines and CM sites and represent the company in front of customers and certification bodies' audits.
Requirements:
Bachelors degree in Electrical Engineering, Mechanical Engineering, or related field.
5+ years of experience in quality / engineering / reliability in a high-tech environment (multi-disciplinary systems - including HW and SW).
Hands-on experience with manufacturing processes: PCBAs, mechanical parts, system integration, and ATE SW.
Experience working with manufacturing partners/CMs and suppliers on quality topics.
Proven experience with CE, EMC, FCC, Safety, WEEE, RoHS in product development and certification processes.
Strong knowledge of quality methods and tools: FMEA, 8D problem solving, root cause analysis.
Strong analytical skills and the ability to interpret test and field data and convert it into concrete actions.
Excellent communication skills in English (written and verbal) and ability to influence cross-functional teams.
Quality certifications (e.g., CQE, Six Sigma Green/Black Belt, Lead Auditor) are an advantage.
This position is open to all candidates.
 
Show more...
הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8479771
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 :)
30/12/2025
Location: Afikim
Job Type: Full Time and English Speakers
we are looking for a Supplier Quality Engineering (Electronics).
As Supplier Quality engineer, you will have responsibility for leading quality assurance day to day quality activities and projects. This role provides quality support for operations, manages our contract manufacturing suppliers (quality/eng oriented) and ensure the overall quality of manufactured products, support and monitoring the production and processes to meet high quality standards. You will also be the leader in defining and implementing quality systems and processes to drive continuous product and process improvement
Responsibilities:
Day-to-day quality engineering activities such as product quality documentation, customer complaints, ECOs, product deviation, non-conformities, FAI, Document control and fields corrective action.
Mange/Support investigations of escalation, deviations, CAPAs, risk assessments, FMEA, root-cause analysis activities internal or supplier sites.
Responsible for leading and implementing IPQC, IQC, OQC approval to supplier
Collect, analyze, and interpret statistical data, perform analyses, and provide reports as required.
Develop and maintain successful external auditing plans for Suppliers and their 2nd tier.
Collaborate with Operations, R&D QA, Engineering and Manufacturing functions to ensure quality standards are in place.
Validation of manufacturing process to meet targets, production output and quality standards
Requirements:
Sc. in Electronic Engineering from a leading university or equivalent experience
+3 Years of Quality Assurance experience in Engineering & manufacturing/NPI environment of multidisciplinary products (Electronics, Mechanic, SW, Testing, Integration)
Alternatively mechanical production engineering with proven experience is acceptable
Ability to read/understand technical drawings
Experience in leading quality projects or project management
Experience in application of risk management techniques (FMEA, FTA) in supporting of design, production and sustain product activities
Proven experience with Turn-key project management and suppliers local and oversea
Excellent communication skills, both verbal and written in English & Hebrew
This position is open to all candidates.
 
Show more...
הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8479671
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 :)
21/12/2025
Location: Yokne`am
Job Type: Full Time
We are now looking for a Senior Hardware Quality Engineer. This role leads the quality strategy and execution across the entire product development lifecycle, ensuring adherence to robust engineering standards and organizational goals. You will drive cross-functional alignment, manage risks, and champion proactive quality measures and continuous improvement initiatives. The mission is to deliver high-quality products by optimizing development, verification, and validation processes from concept to mass production.
What youll be doing:
Define and execute department goals and key performance measures in alignment with the organizations mission, vision, and values; design, develop, and lead quality processes and methodologies.
Provide strong cross-functional leadership, collaborating closely with the relevant project functions to ensure professional, robust execution of every development phase in compliance with engineering standards and quality requirements.
Lead proactive quality activities across the development cycle, including inquiries, Root Cause Analysis (RCA), and the implementation of effective Corrective and Preventive Actions (CAPA).
Drive risk identification and management across the development stages-identifying, prioritizing, tracking, and mitigating risks to prevent schedule or quality impact.
Manage product changes and maintain full configuration control throughout the product development lifecycle.
Promote early detection and rapid issue resolution by driving early reviews, continuous monitoring, effective containment, and correction mechanisms.
Ensure adherence to quality control plans and development processes, continuously enhancing design, verification, and validation practices to safeguard product quality across the full lifecycle of adapters and system products.
Partner with Continuous Improvement to lead and support quality-focused improvement initiatives aimed at reducing customer complaints and internal scrap, while coordinating department-level project planning.
Requirements:
B.Sc. in Electrical / Mechanical/ Material/ Industrial management Engineering, or similar or equivalent experience.
8+ years of experience in the Hardware design development or testing arena or as Process Engineer.
Preferably 5+ years in the field of quality assurance.
Experience in manufacturing process or test engineering, board design/assembly or semiconductors knowledge and previous experience.
Background with hardware qualification, reliability processes, quality procedures and tools.
Familiarity with quality methods Risk assessment failure analysis and FMEA.
This position is open to all candidates.
 
Show more...
הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8465589
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 :)
לפני 20 שעות
חברה חסויה
Location:
Job Type: Full Time and English Speakers
Design Quality Engineer is responsible for driving exceptional product quality for the patient safety, customer value beyond expectations, regulatory assurance, and optimized Cost of Quality for the Company. This is a key technical position, affecting part quality for both installed base and NPI products.
In this role, you will
Daily duties include supporting the project team (R&D, SQA, Product, System and so on) during the development of a project. Our engineers review each design input and output deliverable throughout the development process and resolve compliance impediments as they arise. As a senior engineer the candidate will be responsible for defining two major evolving components in our work:
Implementing AI in our processes - What are the regulatory requirements for implementing AI in a medical device and how to implement it in our development lifecycle.
Cybersecurity work instructions in compliance with the new FDA guidance, train the various teams on the guidance and its implications to our process, and establish best practices for supporting post market vigilance.
Requirements:
Bachelor's Degree in an engineering or equivalent
At least 4-6 years of experience in quality engineering in the medical device industry- Must
Fundamental knowledge of ISO13485:2016 and FDA requirements (e.g. CFR Part 820) EU Medical Device Directive & new MDR, ISO 14971, IEC 62366 and ISO 62304 standards for the medical devices industry
DHF compilation, including Design Controls process and other applicable regulatory, QA and GMP aspects.
Skilled in product risk assessment, requirements management and tracing, defect tracking, configuration management and how they are applied in the product development lifecycle.
Good ability to comprehend multi-disciplinary systems and processes
Effective problem solving, root-cause analytical skills to lead and influence others to drive change (cross-functionally and globally).
Ability to work independently with minimal supervision
Computer skills (Microsoft Word, Excel, PowerPoint)
Working knowledge in Statistical Tools, e.g. miniTab (Measurement Systems Analysis, Process Capability and Statistical Process Control)
Knowledge of various quality system methodologies Lean, 5 Whys, DFMEA, PFEMA, PPAP, etc. preferred
Strong written and verbal communication skills
Strong organizational skills
Excellent written and spoken English
This position is open to all candidates.
 
Show more...
הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8505893
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 :)
לפני 10 שעות
חברה חסויה
Job Type: Full Time
DustPhotonics is developing a cutting-edge technology in Silicon Photonics which is revolutionizing connectivity and communication in data centers. Silicon photonics is becoming a standard technology used for high performance systems, solving challenges of performance, integration, power and cost. This technology is growing rapidly also in other markets such as Healthcare, LIDARs and other sensors. At DustPhotonics, we are looking to solve the difficult problems, in a smart and simple way, by thinking out of the box, leveraging the knowledge and know-how of the team members, and work as team to create Magic. Our Company culture is characterized by accountability for our ethics, for being fair to every employee, customer, supplier and partner. We believe we must work hard and have fun on the way to success. We welcome you to join our team - Apply for your next career opportunity with us! We are looking for a Silicon Engineering Manager Job description As the Silicon Engineering Manager you will be responsible for improving silicon-photonics yield and performance through data-driven analysis, cross-functional collaboration and proactive issue resolution. You will serve as the key interface between R&D, Process and Production teams, ensuring efficient data flow, rapid issue identification and continuous process improvement across wafer fabrication, device testing, and packaging stages.

Responsibilities:

* Perform silicon process and chip-level data analysis, establishing correlation between chip and wafer performance.
* Lead process debug and yield loss analysis at chip/wafer level, driving root cause investigations and corrective actions.
* Manage engineering approval forum to release production material.
* Collaborate closely with vendors to implement new product tests and resolve technical/process issues.
* Act as a key interface between design, testing, and production teams, ensuring alignment across the product lifecycle
* Oversee and coordinate the transfer of data related to silicon design, testing, fabrication, and characterization between Production and R&D departments.
* Develop and implement data management strategies to ensure data accuracy, security, and accessibility.
* Maintain proper documentation of data transfer protocols, version control, and data integrity checks.
* Support data analysis efforts to improve silicon performance, yield, and quality.
* Ensure compliance with company policies and industry standards related to data security and confidentiality.

Hiring Manager:
Arie Faitelson
Requirements:
* B.Sc. or higher in Electrical Engineering, Physics, Materials Science or a related discipline.
* 5+ years of experience in semiconductor or silicon-photonics process, test or yield engineering.
* Proven experience performing silicon process and chip-level data analysis, establishing correlations between chip and wafer performance.
* Hands-on experience in process debug and yield loss analysis, including root cause investigations and implementation of corrective actions.
* Strong technical understanding of silicon device fabrication, testing and characterization processes.
* Experience coordinating data flow and communication between R&D and Production teams.
* Proficiency in data analysis and management tools (e.g., Python, MATLAB, SQL, JMP).
* Excellent problem-solving, analytical and communication skills with attention to detail.
* Ability to work effectively in a cross-functional environment and manage multiple priorities.
This position is open to all candidates.
 
Show more...
הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8374436
סגור
שירות זה פתוח ללקוחות VIP בלבד