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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.

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.
Collaborate with Engineering, Manufacturing, Procurement, and R&D teams to resolve supplier quality issues.
Travel to supplier sites as required.

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 company's 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. Customer Quality
* Lead customer quality responses and investigations.
* Manage customer complaints and field quality issues.
* Support customer audits and quality assessments.
* Develop quality metrics that improve customer satisfaction and product reliability. Quality Culture & Continuous Improvement
* Promote a company-wide culture where quality is everyone's responsibility.
* Train employees on quality systems, best practices, and continuous improvement methodologies.
* Define, monitor and continuously improve Quality KPIs that drive operational excellence. Leadership
* Build and mentor the Quality organization as the company grows.
* Collaborate across R&D, Engineering, Operations, Supply Chain and Executive Leadership.
* Serve as the company's quality advocate internally and externally.

We are looking for a Process Validation Engineer to join our Operations Engineering team and play a key role in ensuring the quality, compliance, and reliability of our manufacturing processes and equipment within a global medical device environment.

In this role, you will lead and support validation and risk management activities across internal and external operations, helping ensure compliance with FDA and ISO requirements while driving continuous improvement initiatives.
You will be responsible for managing validation programs, maintaining risk management documentation, supporting audits, and collaborating closely with cross-functional teams to ensure high standards across systems, products, and processes.

This position requires a strong combination of technical expertise, analytical thinking, organizational skills, and the ability to manage multiple priorities in a fast-paced and highly regulated environment.

Success in this role means becoming a trusted subject matter expert for validation and risk-related activities, driving projects forward with a high level of ownership, maintaining strong collaboration with internal and external stakeholders, and ensuring compliance and operational excellence across validation processes.

What you will do:
Lead the creation of high-level test plans, validation assessments, and validation plans, while overseeing execution progress and completion.
Review and approve test methods, validation test plans, and validation results.
Manage validation samples and support validation execution activities across internal and external operations.
Serve as a point of contact for subcontractor test laboratories and support coordination of validation-related activities.
Maintain and regularly update pFMEA documentation and related risk management records.
Identify risks, support mitigation planning, and implement actions to maintain compliance and process reliability.
Support and conduct internal audits according to the annual audit program and report audit findings.
Manage relevant Issues, NCMRs, and CAPAs related to validation and quality activities.
Serve as a Subject Matter Expert (SME) for validation activities during internal and external audits.
Support continuous improvement initiatives related to systems, products, services, and validation processes.
Participate in and support calibration and preventive maintenance programs for measuring devices and test equipment, as needed.

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.

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

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 multi-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:
Lead multi-functional teams to guarantee seamless completion of all development stages, adhering closely to technical guidelines and quality criteria.
Ensure the professional and robust execution of all development phases, strictly adhering to engineering standards and defined quality requirements.
Drive proactive quality activities such as Inquiry, Root Cause Analysis (RCA), and implement effective Corrective and Preventive Actions (CAPA).
Identify, prioritize, track, and mitigate potential risks to prevent impact on schedule and quality.
Manage product changes and maintain configuration control throughout the development lifecycle.
Promote and enforce early detection mechanisms by driving the implementation of early checks, continuous monitoring, and rapid resolution of identified issues.
Ensure the organization is maintaining adherence to quality control plans and processes; maintain and enhance product design development, verification, and validation processes, to allow high quality of products throughout the entire product life cycle.
Partner with Continuous Improvement to drive Quality process improvement initiatives to reduce customer complaints and internal scrap, including developing and coordinating department project planning.

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.

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.