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05/10/2026
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מיקום המשרה:מרכז
סוג משרה: משרה מלאה
משרות דומות שיכולות לעניין אותך
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1 ימים
Location: Ness Ziona
Job Type: Full Time
The Quality Engineer will be responsible for supporting and maintaining quality processes across production, development, suppliers, and customer-related activities.

Main Responsibilities

Define, write, and oversee quality inspection and testing activities, including IQC, IPQC, and OQC, in both production and development environments.
Manage nonconformance processes, including MRB activities, CAPA follow-up, and customer complaints.
Write, update, and implement quality procedures, work instructions, and quality-related documentation.
Prepare the organization for ISO 9001 audits and lead internal and external audit activities.
Support supplier quality management, including supplier performance monitoring, quality issues, and corrective actions.
Monitor final product and process performance, analyze quality data, and report abnormal trends or recurring issues.
Work closely with Engineering, Production, Supply Chain, and R&D teams to ensure effective implementation of quality requirements.
Drive continuous improvement activities to improve product quality, process stability, and compliance.
Requirements:
up to 2 years of experience as a Quality Engineer in a manufacturing, multidisciplinary, medical device, electro-optical, electronics, defense, or similar technology environment.
Hands-on experience with production quality processes, including IQC, IPQC, OQC, inspection plans, and product release activities.
Experience with nonconformance handling, MRB activities, CAPA, customer complaints, and supplier quality issues.
Ability to analyze quality and production data, identify trends, and report abnormal findings clearly.
B.Sc. in Engineering, Science, or another relevant technical field - required.
Relevant quality certifications, ISO 9001 auditor training, or formal quality assurance training - advantage.
High attention to detail, accuracy, and ability to work according to defined procedures and deadlines.
Ability to work independently, manage priorities, and drive execution across multiple interfaces.
Strong written and verbal English & Hebrew skills.
This position is open to all candidates.
 
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הגשת מועמדות
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8852244
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חברה חסויה
Job Type: Full Time
s we continue to grow, we are seeking an experienced Quality Director to build, lead, and continuously improve our company-wide Quality Management System (QMS) while fostering a culture where quality is embedded into every stage of product development and manufacturing.

As the key member of the Operations leadership team, The Quality Director will be responsible for defining, implementing, and driving quality systems, processes, and culture across the entire organization from product definition and R&D through engineering, operations, manufacturing, supplier management, and customer support.
Responsibilities
Quality Management System
Own and continuously improve the companys Quality Management System (QMS).
Ensure compliance with ISO 9001 and other applicable industry standards.
Develop, implement and maintain company-wide quality policies, procedures and work instructions.
Lead internal and external quality audits and ensure timely closure of findings.
Drive management reviews and quality performance reporting.

Product Development Quality
Integrate quality methodologies into the product development lifecycle.
Partner with R&D and engineering teams to establish Design for Quality (DfQ) practices.
Participate in design reviews, risk assessments, FMEA activities and product qualification.
Ensure appropriate validation and verification processes are implemented.

Manufacturing & Operations Quality
Establish quality controls throughout manufacturing and production.
Define inspection plans, acceptance criteria, and process controls.
Monitor manufacturing yield, reliability, and field performance.
Lead root cause investigations using structured problem-solving methodologies (8D, 5-Why, Fishbone, etc.).
Drive corrective and preventive actions (CAPA).
Own product quality throughout the entire product lifecycle, from product development through manufacturing and customer deployment.

Supplier Quality
Develop supplier qualification and monitoring processes.
Conduct supplier audits and performance reviews.
Work closely with contract manufacturers and component suppliers to ensure consistent quality.
Drive supplier corrective actions and continuous improvement initiatives.
Requirements:
B.Sc. in Engineering or related technical discipline.
8+ years of quality management experience in high-tech hardware manufacturing companies.
Experience implementing and managing ISO 9001 Quality Management Systems.
Experience supporting product development from concept through production.
Strong knowledge of quality tools including: CAPA, FMEA, SPC, 8D, Root Cause Analysis, Control Plans.
Experience working with silicon suppliers, contract manufacturers.
Excellent communication and leadership skills and Strong analytical and problem-solving capabilities.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8827075
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חברה חסויה
Location: Shlomi
Job Type: Full Time
We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.

Job Summary
In this fully onsite role, the Manufacturing Quality Engineer will own all qualiy activities at one of the manufacturing sub-contractors, support the validation process to the contract manufacturing and provide quality oversight to the engineering department, while working within a multi-functional team environment for medical devices. The Manufacturing Quality Engineer will lead projects and tasks, from product validation through transfer to the production and play an active role to ensure products meet quality standards consistent with internal procedures and acceptance criteria. Additionally, this role will identify and implement improvements to the production processes. The Manufacturing Quality Engineer will be the products and production focal point for our sub-contractors and will be responsible for projects related to the production and machines, including training, audits, stop and renew the production.

Essential Duties and Responsibilities
Exhibit a strong quality first mentality and ensure that product and quality are held to the highest standard.
Work cross-functionally with individuals or extended teams to provide guidance and ensure success of projects.
Responsible to write, review and approve pilot documents (including reports).
Write and approve various department and production procedures and forms.
Lead investigation processes for deviations and nonconformities in production and create analysis reports.
Responsible to train the sub-contractors according to QA procedures and VoE.
Support special processes such as sorting or rework in production.
Own all production activities at one of the subcontractors to ensure manufacturing is held according to West procedures and GMP/GDP standards
Responsible for stopping and renewing production with accordance to West requirements and with MQ manager approval.
Manage production related projects and act as MQ focal point in various internal and external projects- such as Data Integrity, CoPQ, production improvement plans, etc.
Provide Quality oversight of validation activities and processes.
Lead pilot processes that include change and approval of quality aspects in pilot protocols and reports and assure that pilot processes are conducted according to West guidance and protocols.
Attend production pilot meetings as the MQ focal point.
דרישות:
Education
Bachelor's Degree in Engineering or science related- required.
Relevant work history and/or experience may be considered in lieu of degree.
Work Experience
Minimum 3 years of experience in a quality engineering role in a regulated industry, pharmaceutical, or medical device manufacturer- required.
Preferred Knowledge, Skills and Abilities
Experience with production processes and process controls.
Experience with sub contractors interface and meeting customer expectations.
Experience with Medical Device, Validation Activities, Risk Management, Product Transfer to production.
Working knowledge of quality systems such as ISO 13485, 21 CFR 820, ISO 14971, MDSAP.
Must have effective problem solving and interpersonal skills.
Ability to work independently, multi-task and thrive in fast-paced environment.
Problem solving including root cause failure analysis methods.
Additional Requirements
Minimum 3 years of experience in Medical Device Quality & Production lifecycle.
Experience with production processes and process controls.
Experience with sub contractors interface and meeting customer expectations.
Experience with Medical Device, Validation Activities, Risk Management, Product Transfer to production.
Working knowledge of quality systems such as ISO 13485, 21 CFR 820, ISO 14971, MDSAP.
Must have effective problem solving and interpersonal skills.
Ability to work independentl המשרה מיועדת לנשים ולגברים כאחד.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8827725
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Location: Ra'anana and Shlomi
Job Type: Full Time and Hybrid work
This role will be required to travel to our sister site in Shlomi 3x per week and at Ra'anana site 1x per week and 1 day working remote.

In this role, The Sr Manager, Quality Engineering is responsible for leading the sites Quality Engineering, Manufacturing Quality, and Quality Compliance functions. This role oversees engineering quality processes, design transfer, process validation, production quality oversight, customer complaints handling.

The Sr. Manager, Quality Engineering position leads Quality Engineers for both design and operations and Quality compliance engineers and ensures that products, processes meet all applicable regulatory, customer, and corporate requirements. The Manager serves as a strong advocate for product and process quality across the full lifecycle - from design transfer and process validation through post-market surveillance.

This role works cross-functionally with Operations, Engineering, RA, Supply Chain, and external stakeholders, ensuring compliance with standards such as ISO 13485, MDR 2017/745, MDSAP, ISO 14971, 21 CFR 820, and applicable GMP requirements.

Essential Duties and Responsibilities
Quality Engineering & Manufacturing Oversight: Lead review and approval of technical and engineering documentation including: DMR, DHF elements, IQ/OQ/PQ, Process validations and qualifications, Product specifications. Risk management files (dFMEA/pFMEA), Test methods, protocols, reports, Design transfer documentation.
Provide quality oversight for: New production line establishment Process validation activities Engineering changes (ECO/DCO), Software validations.
Oversee production quality controls including: Raw material approval, Calibration approval (including deviations), DHR and batch record review, Labeling release, Nonconformance management (NCMR).
Drive Right First Time and Cost of Poor Quality (CoPQ) initiatives.
Provide escalation support and structured problem-solving guidance.
Customer Complaints & Post-Market Surveillance: Lead the sites customer complaints handling process:
Investigation and root cause analysis, Risk-based evaluation, Corrections and corrective actions, RMA/RGA management, Oversee complaints trending and reporting.
Support RA in identification of Adverse Events and Hazardous Situations.
Ensure feedback loop into risk management files and process improvements.
Interface directly with customers regarding QA-related nonconformities and investigations.
Leadership & People Management; Set priorities and objectives for Quality Engineering and Compliance teams. Supervise day-to-day performance, training, and development.
Provide coaching on: Root cause analysis, Risk-based decision making, Regulatory interpretation, Technical problem solving, Ensure effective communication across functional and leadership levels.
Promote a strong Quality First culture throughout the organization.
Requirements:
Education
B.Sc. in Engineering, Science, Chemistry, Biology or related discipline (Relevant experience may be considered in lieu of degree).

Work Experience
8-10+ years of experience in Quality roles within Medical Device industry.
Proven experience in:
Design controls

Process validation

Risk management

Customer complaints handling

Strong knowledge of: ISO 13485, MDR 2017/745, MDSAP, ISO 14971, 21 CFR 820.
5+ years of people management experience, preferred experience of managing team leaders..
Preferred Experience with: MasterControl, SAP, SharePoint, Statistical tools, Proficient in Microsoft Office Suite.
Preferred Knowledge, Skills and Abilities
Certified Quality Auditor preferred.
Strong knowledge and understanding of FDAs 21 CFR Part 820, ISO13485, ISO9001, and other international regulations.
Familiarity with document management databases, particularly MasterControls and SAP.
Proven ability to manage multiple priorities, drive projects to completion and meet internal customer expectations.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8827732
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חברה חסויה
Location: Rehovot
Job Type: Full Time
Required Quality & Reliability Lead
What we are looking for:
The Quality & Reliability Engineer is responsible for driving product quality, manufacturing excellence, and reliability performance across our products and operations.
Working closely with Engineering, Manufacturing, Supply Chain, Service, and R&D teams, this role leads quality and reliability initiatives that improve process capability, manufacturing yields, product robustness, and customer satisfaction through data-driven decision making, structured problem solving, and continuous improvement methodologies.
The role is also expected to leverage AI and advanced analytics tools to accelerate insights, improve decision making, and enhance operational effectiveness.
Responsibilities
What will you be doing:
Responsibilities - Quality:
Lead quality improvement initiatives focused on yield enhancement, defect reduction, process stability, and continuous improvement across DMD operations.
Establish and maintain Statistical Process Control (SPC) and drive process capability analysis using statistical methods and data-driven quality metrics.
Lead root cause investigations utilizing methodologies such as 8D, 5 Why, Fishbone Analysis, Pareto Analysis, DOE, and FMEA.
Drive NCR, CAPA, and corrective action processes, identify trends, prioritize actions using evidence-based analysis, and verify effectiveness of implemented solutions.
Partner with Manufacturing, Engineering, Service, and Customer Support teams to resolve product quality issues, customer complaints, field incidents, and escalations.
Collaborate with suppliers to improve quality performance, drive supplier corrective actions, and reduce supplier-related quality risks.
Conduct supplier audits and assessments, including evaluation of manufacturing controls, process capability, inspection methods, and process discipline.
Review supplier quality documentation including CoC, CoT, ATR, inspection records, and quality reports to identify risks, trends, and improvement opportunities.
Lead internal and external audits, ensuring compliance and effective corrective actions.
Responsibilities - Reliability:
Partner with Engineering and R&D teams to define reliability qualification plans, test strategies, acceptance criteria, and reliability requirements for new and existing products.
Ensure reliability testing programs are properly executed and that test results are systematically reviewed, analyzed, and translated into actionable improvements.
Partner with Service and analyze reliability, field performance, MTBF, and MTTR data to identify trends, emerging risks, and improvement opportunities.
Lead investigations of reliability failures and support identification of physical, mechanical, electrical, optical, material, and process-related failure mechanisms.
Requirements:
B.Sc. in Mechanical, Electrical, Materials, Industrial Engineering, or a related technical discipline.
5+ years of experience in Quality Engineering, Reliability Engineering, Manufacturing Quality, or Product Quality within a high-tech manufacturing environment.
Strong hands-on experience with SPC, Process Capability Analysis, DOE, statistical analysis, root cause investigation, and corrective action methodologies.
Experience with reliability testing, qualification programs, reliability data analysis, and failure analysis.
Experience in semiconductor equipment, semiconductor manufacturing, or multidiscipline platforms in advanced technology industries. - An advantage
Working knowledge of ISO 9001, SEMI standards, and semiconductor reliability qualification practices. - An advantage
Experience leveraging AI, automation tools, and advanced analytics to improve engineering, quality, reliability, or operational processes is a strong advantage. - 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
8866883
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01/10/2026
חברה חסויה
Location: Netanya
Job Type: Full Time
Required QA Specialist
Description
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 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:
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
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8838891
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תודה על שיתוף הפעולה
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Location: Ra'anana
Job Type: Full Time and English Speakers
We are looking for an experienced Quality Assurance Engineer to lead and coordinate the company's quality activities across subcontractors and suppliers in Israel and internationally. The role is responsible for supplier qualification, continuous product and process improvement, and ensuring end-to-end product quality.
This position includes close collaboration with local and global subcontractors, electronic and mechanical assembly lines, and ownership of implementing a strong quality culture throughout manufacturing and shipping operations.
Responsibilities include ensuring workforce qualification at subcontractor sites (including work instructions, training, preventive and corrective actions, and audits), reviewing and approving production deviations, defining quality improvement KPIs and monitoring their implementation, supporting New Product Introduction (NPI) activities, monitoring engineering change implementation, ensuring the latest product revisions are used in manufacturing, participating in reliability and regulatory compliance activities, and generating quality performance reports for both operations and subcontractors.
The role involves extensive cross-functional collaboration throughout the organization.
If you have a systems-oriented mindset, deep understanding of manufacturing and assembly processes, and proven experience in high-tech or defense companies, we'd love to hear from you.
Requirements:
At least 7 years of experience as a Quality Assurance Engineer in a hardware manufacturing environment.
Extensive hands-on experience working with subcontractors and suppliers.
Strong knowledge of quality management standards such as AS9100 and ISO 9001.
Deep understanding of electronic manufacturing processes, including PCB, PCBA, SMT, and IPC standards.
Strong understanding of mechanical manufacturing processes, including machining, sheet metal, enclosures, painting/coating, complex mechanical assemblies, tolerancing, and fits.
Proven experience leading Root Cause Analysis and implementing corrective and preventive actions using methodologies such as CAPA, 8D, and 5-Why.
Preferred Qualifications & Skills
Bachelor's degree in Industrial Engineering, Mechanical Engineering, Electrical/Electronics Engineering, Quality Engineering, or a related field.
Strong leadership skills with the ability to drive cross-functional initiatives independently.
Experience working with multiple stakeholders, including R&D, Engineering, Procurement, Manufacturing, and suppliers.
Experience with ERP and PLM systems.
Advanced proficiency in Microsoft Office, particularly Excel.
Strong understanding of operational and logistics processes.
Ability to work effectively under pressure in a fast-paced environment.
Self-motivated, proactive, and highly organized.
Excellent interpersonal, communication, and customer-oriented skills.
Professional assertiveness and strong problem-solving abilities.
Fluent English, both written and spoken (mandatory).
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8832890
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תודה על שיתוף הפעולה
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28/09/2026
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 a 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 NPI 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
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8730161
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מודים לך שלקחת חלק בשיפור התוכן שלנו :)
לפני 6 שעות
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 experienced Production Quality Engineer with a proven track record in leading failure investigation processes for its manufacturing site in Beit Shean. Responsibilities:
* Lead quality investigations for failure events and non-conformities, including root cause analysis and driving corrective and preventive actions.
* Conduct internal audits, including familiarity with aerospace standards, and track and monitor identified gaps.
* Analyze data and present trends and statistics on an ongoing basis.
* Develop improvement plans and monitor their implementation and effectiveness.
* Work cross-functionally (R&D, Engineering, Procurement, Manufacturing) with products in the NPI phase.
* Prepare presentations and lead meetings with multidisciplinary teams.
* Take overall responsibility for quality processes in military product manufacturing, including FMEA and MRB handling.
* Read and interpret engineering specifications and technical drawings at a high level.
* Utilize computer applications effectively, including presentations, with clear and concise communication in English.
Requirements:
* Degree in Quality Engineering, Industrial Engineering & Management, or Practical Electronics Engineering (technological background – advantage).
* At least 2 years of experience in quality roles (Quality Engineer or Quality Team Lead).
* Background in electronic and mechanical assembly environments.
* Familiarity with aerospace standard AS9100 – advantage.
* Experience leading failure investigations with multidisciplinary teams.
* High level of English – mandatory
* Strong proficiency in Microsoft Office, including Excel and presentation tools; ability to prepare and deliver professional training materials in Hebrew and English.
* Strong analytical skills, attention to detail, ability to work independently and close tasks effectively.
* Ability to read and understand test documents, technical specifications, and drawings – mandatory.
* Ability to write clear and concise procedures and work instructions.
* Familiarity with IPC standards for electronics and mechanics – advantage.
* Excellent interpersonal skills, teamwork, and ability to work across multiple interfaces.
* Ability to work in a dynamic and high-pressure environment, with willingness to work overtime.
* Full-time, on-site position.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8813893
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14/09/2026
חברה חסויה
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 a motivated and experienced Supplier Quality Engineer to join our team! As a Supplier Quality Engineer, you will be responsible for managing supplier programs for manufacturing and ensuring that quality programs follow regulatory requirements. Supplier Quality Engineer duties and responsibilities
* Driving supplier quality performance, including new product development and product quality improvement
* Providing leadership and management for the supplier quality department
* Ensuring the supplier meets all regulatory and company requirements.
* Performing quality system audits
* Establishing quality control objectives & Maintaining supplier quality records
* Promoting initiatives to improve quality.
Requirements:
Requirements:
* Minimum of a bachelor’s degree in a related field (electronics / Quality).
* Relevant education in quality CQE/CQM- advantage.
* Familiarity with mechanics production standards and special processes, paint and coating.
* Strong problem-solving skills.
* Minimum of 3 years of experience in a similar role.
* Strong technical skills.
* Knowledge and experience reading drawings.
* Excellent verbal and written communication skills.
* Excellent analytical skills.
* Ability to work well in a team 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
8761350
סגור
שירות זה פתוח ללקוחות VIP בלבד