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משרה בלעדית
לפני 16 שעות
דרושים בריקרוטיקס בע"מ
Job Type: Full Time
A medical device company is looking for a Quality Engineer to join our team.
Responsibilities Communication and collaboration with customers and suppliers, including: Documentation and handling of customer complaints.
Internal and supplier-related non-conformities (NCMRs).
CAPA - Conducting thorough investigations using standard tools such as 5 Whys, Fishbone diagram, and process flow mapping.
Preparation and management of Change Orders across departments through to release.
Requirements:
CQE-certified Quality Engineer and/or a degree in Industrial Engineering, Chemistry, or Life Sciences - preferred.
At least 5 years of experience in the field of quality.
This position is open to all candidates.
 
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8811645
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משרה בלעדית
1 ימים
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 talented Program Quality Engineer to join our team.

Key Responsibilities:

Lead Quality Assurance across the hardware development lifecycle for radar systems
Ensure quality from design through verification and pre-production
Develop and execute quality plans for hardware development projects
Lead SRR, PDR, CDR, TRR, and PRR
Define and track quality KPIs
Conduct FMEA for RF, power, thermal, structural, and integration elements
Support verification, reliability, and environmental testing
Approve TEST plans and reports
Manage change control and traceability
Support AS9100 and MIL- STD compliance
Lead root cause analysis and corrective actions
Collaborate with suppliers and cross-function
Requirements:
Requirements
Bachelors degree in Electrical, Mechanical, Aerospace Engineering, or a related field
5+ years of quality engineering experience in complex hardware environments
Experience in AS9100-regulated development
Familiarity with FMEA, Six Sigma, and APQP/PPAP
Ability to analyze schematics, drawings, TEST data, and failure reports
Experience in radar, aerospace, defense, or automotive is an advantage
Added Advantage
CQE certification
Knowledge of environmental and reliability testing
Familiarity with DFM/A, ICT, and AOI
This position is open to all candidates.
 
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8790083
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משרה בלעדית
1 ימים
דרושים בQHR
Job Type: Full Time
Provide on-the-floor QA oversight during sterile manufacturing activities, including aseptic processing, filling, filtration, cleaning, set-up, line clearance, and routine production
Ensure Real-Time compliance with approved batch records, SOPs, GMP requirements, aseptic practices, gowning, material/personnel flow, and contamination control expectations
Review and verify GMP ation during the shift, including batch records, logbooks, forms, line clearance records, equipment status, and critical process entries for accuracy, completeness, and data integrity
Identify, assess,, and escalate quality events, deviations, documentation errors, process anomalies, EM concerns, and potential contamination risks in real time
Support deviation initiation, impact assessment, containment actions, investigation inputs, CAPA follow-up, and batch-related quality decisions with Production and QA man
Requirements:
B.Sc. in Life Sciences, Biotechnology, Biology, Microbiology, Chemistry, Pharmacy, Chemical Engineering, or a related scientific discipline- Must
Additional GMP, aseptic processing, contamination control, or quality systems training - Must
5+ years of QA, production, or quality oversight experience in sterile pharmaceutical manufacturing
Practical GMP experience in cleanrooms, aseptic processing, batch documentation, line clearance, deviations, CAPA, and production-floor investigations
Good understanding of contamination control, EM, gowning practices, cleanroom behavior, aseptic interventions, and data integrity principles
Ability to work independently on the production floor, make risk-based decisions, and escalate issues appropriately
This position is open to all candidates.
 
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8810164
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דרושים בU-MAN השמה
סוג משרה: משרה מלאה
לחברת הנדסה ותיקה ומובילה, מתמחה בפתרונות הנדסיים בתחומי אוטומציה, מכניקה ועוד. למגוון רחב של תעשיות.
דרוש/ה: מנהל /ת אבטחת איכות.
התפקיד כולל:
ניהול והובלת מערך האיכות בארגון ושיפור מתמיד של תהליכי האיכות
ניהול צוותי ביקורת קבלה וביקורת סופית והגדרת קריטריונים לבקרה
ביצוע בקרות איכות בתהליך והובלת פעולות לשיפור תהליכים
טיפול בתקלות איכות, ניתוח גורמי כשל והובלת פעולות מתקנות
כתיבה, עדכון והטמעה של נהלים ומפרטים בהתאם לתקני איכות
הובלת מבדקים פנימיים וחיצוניים ועמידה בתקני ISO
ביצוע מבדקי איכות לספקים, דירוג ספקים והובלת תהליכי שיפור
ביצוע בדיקות FAI
הובלת הדרכות מקצועיות והסמכות עובדים בנושאי איכות ותקנים
העבודה בפתח תקווה
דרישות:
תואר ראשון בהנדסת איכות / הנדסת תעשייה וניהול / הנדסה רלוונטית - חובה
ניסיון של לפחות 5 שנים בניהול איכות בתעשייה - חובה
ניסיון בעבודה עם תקני איכות ותקני ISO
ניסיון במערכת פריוריטי - יתרון משמעותי
אסרטיביות מקצועיות, יכולת קבלת החלטות
תקשורת בינאישית טובה ויכולת עבודה בשיתוף פעולה מול ממשקים רבים בארגון. המשרה מיועדת לנשים ולגברים כאחד.
 
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הגשת מועמדות
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8810863
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Location: Ra'anana
Job Type: Full Time
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.
Key Responsibilities
Manufacturing Quality Management:
Lead quality assurance activities across electronic and mechanical manufacturing and assembly lines.
Define quality gates, inspection checkpoints, and manufacturing quality control processes.
Drive implementation of quality standards throughout production.
Supplier & Contract Manufacturer Quality:
Lead, monitor, and audit electronic (EMS) and mechanical contract manufacturers.
Qualify suppliers and subcontractors and approve manufacturing processes.
Conduct supplier quality audits and drive continuous supplier performance improvement.
Failure Investigation & Root Cause Analysis:
Lead engineering investigations to identify root causes of manufacturing and product quality issues.
Analyze quality data and failure trends.
Define, implement, and monitor corrective and preventive actions (CAPA, 8D, 5-Why).
Continuous Improvement:
Initiate and lead process improvement projects.
Reduce scrap rates and improve First Time Yield (FTY).
Establish quality KPIs and monitor improvement initiatives.
Requirements:
Mandatory Qualifications:
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.
This position is open to all candidates.
 
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עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8765843
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לפני 7 שעות
חברה חסויה
Location: Kefar Sava
Job Type: Full Time
As a Quality Engineer based in Kfar Saba, you will play a key role in supporting day-to-day quality activities while helping harmonize quality and regulatory processes across the organization. This position focuses on design controls, CAPA, complaint handling, software development lifecycle activities, and regulatory compliance within a regulated medical device environment. You will collaborate with cross-functional teams to ensure quality system requirements are effectively implemented, maintained, and continuously improved, supporting the delivery of innovative technologies that advance patient care.

Responsibilities may include the following and other duties may be assigned:
Assist in aligning and implementing design control processes, including requirements management, design reviews, verification/validation, and traceability.
Support the mapping, migration, and harmonization of quality system processes, including document control, training, audits, and related quality activities; support internal and external audits as applicable.
Participate in the integration and standardization of CAPA and complaints handling processes, ensuring effective root cause analysis, corrective and preventive actions.
Support software development lifecycle processes, including requirements management, design reviews, validation, and testing.
Ensure all integrated processes meet applicable regulatory requirements (FDA, MDR, ISO 13485, 21 CFR Part 11, etc.), including electronic records and signatures, risk analysis, and audit readiness.
Assist in updating and maintaining quality documentation, provide training to stakeholders on new or revised processes, identify process gaps, and support continuous improvement initiatives.
Requirements:
Required Knowledge and Experience:
Bachelors degree in Engineering, Life Sciences, or a related field.
3+ years of experience in medical device quality engineering, including QMS, design controls, CAPA, complaints management, and software validation.
Working knowledge of FDA regulations, MDR, ISO 13485, and 21 CFR Part 11 requirements.
Experience with software development lifecycle processes in regulated environments is an advantage.
Strong analytical, communication, and teamwork skills, with the ability to work effectively in cross-functional environments.
Experience with QMS integration or harmonization projects and electronic QMS platforms would be considered an advantage.


Physical Job Requirements:
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this 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
8813116
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7 ימים
חברה חסויה
Location: Netanya
Job Type: Full Time
Join Orbit Communication Systems as a Student for the QC Team and gain practical experience in quality control, inspections, calibration activities, and quality processes within a multidisciplinary engineering environment.

Responsibilities:
Lead and manage in‑process and final QC inspection activities, including supervision and professional development of QC staff.
Support and maintain the Quality Management System (QMS) in accordance with company and regulatory requirements.
Responsible for calibration management of ORBIT equipment.
Manage employee certification processes (internal and external) and develop annual training plans.
Lead and support continuous improvement initiatives in collaboration with Operations teams.
Review and approve ECO / MCO / ATP / ATR / production documentation, and waivers related to R&D and Engineering.
Lead customer complaint investigations using structured methodologies (8D, RCCA, etc.).
Plan and perform internal quality audits.
Support and participate in external quality audits and certifications (customers, FAA, CAAI, SII, etc.).
Perform and approve First Article Inspections (FAI) in accordance with AS9102.
Monitor failures and ensure effective follow‑up of corrective and preventive actions (CAPA).
Analyze quality trends and performance indicators (Quality Yield, KPIs).
Manage RMA processes and perform quarterly quality data analysis for QBRs.
Prepare Quality Plans (QP) and Quality Improvement Plans (QIP).
Requirements:
Bachelor's degree in Engineering, Quality Management, or related field.
At least 8 years of experience in quality assurance or operations management.
Proven experience with quality control methodologies and tools.
Strong analytical skills with the ability to interpret complex data.
Excellent communication and leadership skills.
Experience in the communications or technology industry is preferred.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8804083
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28/07/2026
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
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8691131
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תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
19/08/2026
חברה חסויה
Location: Netanya
Job Type: Full Time
we are 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 our companys 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
8789152
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מודים לך שלקחת חלק בשיפור התוכן שלנו :)
30/07/2026
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
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תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
חברה חסויה
Location: Ra'anana
Job Type: Full Time
We are looking for a senior Quality Engineer to serve as our main technical expert for hardware quality and environmental compliance from New Product Introduction (NPI) to mass production. In this high-level role, you will be responsible for building our very first quality plan, setting up our quality system from scratch, and writing all standard procedures.
You will lead the company through its initial certifications for both ISO 9001 and ISO 14001 and take full responsibility for keeping them updated. You will also look ahead to prepare our systems for ISO 45001 (Occupational Health and Safety) as we grow. someone with an open-minded and creative approach to finding ways to use AI tools to automate manual quality tasks. Working closely with both software and high density networking hardware teams, you will make sure our products, local and international factories, and global vendors meet top industry standards for reliability and sustainability. This role requires managing quality systems for production lines located both locally and abroad, with a willingness to travel and visit our global lines as needed.
Requirements:
Education: Engineer or Practical Engineer degree, preferably in Electronics, with a formal quality qualification (such as CQE, CMQ/OE, or equivalent certification).
Experience: 10+ years of solid experience in the high-tech industry. Prior experience in networking or telecommunications sectors is a strong advantage.
Global Manufacturing Flexibility: Proven capability managing quality systems across both local and international production lines; must be completely willing to travel and visit our global lines as needed to maintain standards.
System Building Track Record: Proven success building a quality system (QMS) or environmental system (EMS) from scratch, including writing company policies, creating quality plans, and leading initial certification audits.
Manufacturing Standards: Deep understanding of electronic manufacturing standards, with strong practical knowledge of IPC rules (such as IPC-A-610) to define and audit board-level workmanship criteria across local and international production lines.
AI & Automation Mindset: An open-minded and creative approach to using basic scripting (like Python), automation tools, or AI utilities to replace manual data entry and speed up office tasks.
Consultant & Vendor Management: Experience finding, onboarding, and directing external compliance consultants, engineering contractors, and third-party test labs.
Technical Hardware Knowledge: Strong understanding of factory processes, electronic board manufacturing (PCBA), and IPC workmanship rules.
Standards Knowledge: Ability to build and maintain ISO 9001 and ISO 14001 systems from a zero compliance baseline. Good familiarity with managing RoHS/REACH paperwork and basic Greenhouse Gas (GHG) reporting.
Hardware Compliance Knowledge: Basic knowledge of safety and regulatory compliance requirements for hardware appliances (such as CE, FCC, UL, or matching certifications).
This position is open to all candidates.
 
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עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
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