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Quality Engineer is responsible for identifying, analyzing, and correcting failures in products and processes. This role involves close collaboration with Development, Engineering, Production, and Customer service teams to ensure product and service quality.
Responsibilities:
FRACAS Management
Conduct failure analysis for products and processes.
Recommend and implement corrective actions to resolve identified failure modes.
Develop and implement quality control processes for continuous improvement.
Collaborate with cross-functional teams (e.g., design, manufacturing, quality) to understand the issues.
Prepare failure analysis reports and present findings to management.
Follow up on the effectiveness of corrective actions and make adjustments as necessary.
Participate in internal and external Quality audits.
Support the approval processes for new products.
Maintain detailed reports of failure investigations, findings, and corrective actions taken.
Identify opportunities for process or design improvements based on failure trends.
Analyzing Quality trends: Quality Yield , KPIs , CoPQ (Costs of Poor Quality), Customers Rating, RMA, ,Quarterly data analysis for QBR
Investigate and analyze product failures, identifying root causes using techniques such as root cause analysis (RCA), fault tree analysis (FTA), or failure mode and effect analysis (FMEA).

At SolarEdge (NASDAQ: SEDG), we're a global leader in smart energy technology, with over 3,000 employees, offices in 34 countries, and millions of installations worldwide. Our innovative solutions include solar inverters, battery storage, backup systems, EV charging, and AI-based energy management. We're committed to making clean, green energy the primary power source for homes, businesses, and beyond. With the growing demand for electricity, the need for smart, clean energy sources is constantly rising. SolarEdge offers amazing opportunities to develop your skills in a multidisciplinary environment, covering everything from research and development to production and customer supply. Work with talented colleagues, tackle exciting challenges, and help create a sustainable future in an industry that's always evolving and innovating. Join us and be part of a company that values creativity, agility, and impactful work. We invite you to join our manufacturing in north Israel. By being SolarEdge’s Quality Engineer you will have the opportunity to build a full proof quality system to establish the high quality and reliability products that assure the expected long-life warranty of the products. What will you be doing?
*  Define and Implement methods and reporting systems to monitor the quality in all factory related processes.
* Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
* Analyze data and lead over all cross-organization improvements plan
* Lead Failure Analysis investigations and implement cross organization Corrective and Preventive actions
* Represent production quality related issues

Country:
Israel

City:
Ziporit

We are recruiting a quality engineer
our team is growing, and we are looking for you to join us as a QA Engineer to lead and enhance our Quality Assurance processes and methodologies.
what will you do:
be the quality advocate in the company, guiding the team on Quality Assurance architecture and methodologies.
define and execute regression, new feature, and performance testing frameworks with relevant metrics.
develop and implement a strategy for continuous testing efforts in new and upgraded products.
analyze data and communicate TEST results effectively.
use strong analytical skills to solve complex problems while adapting to changing priorities.
interface with internal customers including software development, customer support, documentation, and product planning.
work closely with development, product management, and other teams to design and execute TEST plans for new features.
ensure the quality and reliability of the system through comprehensive testing.
troubleshoot and investigate issues in a complex system structure.

Implementation and leadership of quality processes within the E3D projects
Leading risk surveys, review, and approval of product development documents/design changes
Working with departments in the organization, customers, subcontractors, and suppliers handling customer complaints, quality agreements, procurement specifications, complaints to suppliers, and more
Responsibility for defining the quality assurance requirements in the project and product

A fast-growing global medical device company, developing and manufacturing innovative drug delivery and infusion solutions across the continuum of care- from the hospital to the home. We are looking for an excellent Product Quality Engineer to join the QA product team.
Job Description:
Serve as owner of the NCMR process: manage the end-to-end handling of non-conforming materials, products, and processes, including initiation, investigation and corrective/preventive actions in accordance with company procedures and regulatory requirements.
Support for non-conformity investigations and assign effective corrective actions for NCMRs and ensure timely closure and documentation.
Conduct quality assurance activities such as data analysis and statistical evaluations, SOP review and approvals, audit preparation,
Act as the Design QA representative in R&D project meetings, review and approve project deliverables and documents in accordance with internal SOPs and applicable regulatory standards.
Participate in risk management and evaluation processes related to product development and design changes.
Participate in change control processes for both R&D and commercial products, ensuring quality compliance.

As Supplier Quality engineer, you will have responsibility for leading our company's 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 our company's 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.
Leading and continuously improving companys Quality Management System and quality engineering activities, Monitor, and analyze quality performance and KPI.
Develop and maintain successful external auditing plans for Suppliers and their 2nd tier.
Takes an active role in leading, reviewing, and approving quality manufacturing product changes.
Validation of manufacturing process to meet targets, production output and quality standards.

The QA Engineer is responsible for developing and maintaining the companys Quality Management System in accordance with various medical device requirements.

We are located in Yokneam.

Main responsibilities:

Work closely with the engineering, operations and supply chain teams, both in Israel and the USA, providing ongoing (sustain) product support and supporting NPI activities (e.g., parts and materials specifications, equipment qualification, facility and infrastructure qualification and process controls.
Good mechanical and electrical knowledge to enable conducting process nonconformities investigations and implementation of corrective actions.
Leading and supporting CAPA activities.
Supplier Quality: Approval of new suppliers, analyse suppliers performance, Supplier auditing and SCAR management.
Proactively initiate and support process improvements, through improved process controls, statistical techniques and use of various production related SW tools.
Supporting Computer Software Validation activities both in R&D and production, Understanding 21CFR part11 requirements.
Auditing: Perform internal auditing in accordance with ISO19011 and support all activities related to external audits.

A world-leading material science company, focused on the research, development, manufacturing, and marketing of vision and light control technologies that support safe, sustainable, comfortable, and agile user experiences across various industries.
We are seeking an experienced Quality Assurance Manager to lead our quality initiatives and ensure compliance with global standards. This role is integral to maintaining our high manufacturing standards, driving continuous improvement, and collaborating with cross-functional teams to enhance product quality and performance.
Joining means becoming part of a cutting-edge, fast-growing company that values innovation, excellence, and teamwork in shaping the future of smart materials.

Please send a copy of your CV in English.
Responsibilities
Drive quality performance and continuous improvement across the organization.
Develop and implement product quality assurance strategies across all development phases.
Define QA compliance objectives and ensure adherence to international standards (ISO 9001, VDA 6.3, IATF 16949).
Establish quality control methods, documentation, and risk management practices (FMEA, APQP, PPAP, SPC, MSA).
Investigate root causes of deviations with R&D and production teams, ensuring corrective actions.
Oversee supplier evaluations, internal audits, and customer compliance audits.
Train and supervise technical staff in quality processes, testing, and reporting.
Serve as the product safety representative and liaise with global quality teams.
Prepare for and manage internal, customer, and certification audits.
Willingness to travel internationally when required.

We are looking for a Quality Engineering, Team Leader.
Essential Duties and Responsibilities
Contribute to the development and implementation of quality management programs focusing on continual improvement across various processes.
Create processes to better evaluate, track and trend audit outputs and identify risks/issues and evaluate impact on global quality systems and initiate actions, as needed.
Coordinate communication between internal teams.
Regularly analyze data trends, drive improvements and meet customer expectations through efficient reporting and communication.
Reviews, revises, and creates operating procedures to ensure compliance with all related external requirements, internal procedures or instructions, and the Manual.
Ability to lead meetings with relevant teams, employees and contractors as necessary to manage changes.
Establishes monthly KPIs and metrics to Quality Leadership.
Drive continuous quality improvement projects across the enterprise for increased compliance and to create efficient use of company resources.
Leading personnel responsible for calibration activities monitoring, calibration reports approvals. Responsible for calibration specifications approval and for reviewing and approving calibration deviations.
Lead the sites device sterilization methods establishment, validation, maintenance and routine controls as the site sterilization SME by verifying that the sterilization methods validation is done according to the applicable standards and regulations. Verify the sterilization methods and risk-based approach are routinely maintained. Address sterilization issues and provide solutions to sterilization challenges.

We are looking for Quality Manager with a 5 years experience.
This position will be responsible for overseeing the quality within the company, focusing on the development, implementation, and monitoring of quality methodologies and processes.
The role will be hands-on, including internal quality control, supplier audits, development of quality documentation, and management of multidisciplinary processes within the company.
The Quality Manager will work closely with our development & engineers, production, and regulatory teams to ensure compliance with rigorous quality standards.
Key Responsibilities:
Developing Quality Methodology: Develop and implement comprehensive quality methodologies, focusing on multi-disciplinary products (including hardware, electronics, mmechanics and software).
Hands-on Role: Perform independent quality control, design, and manage continuous quality improvement processes.
USO Certification and Quality Control: Ensure compliance with international quality certifications and standards, such as ISO, and specific defense standards (e.g., MIL-STD).
Supplier Audits: Conduct quality audits for suppliers in the hardware and electronics domains, analyze results, and provide recommendations for improvement.
Organizing Proposals and Processes: Define processes for organizing proposals and ensure quality requirements are met during supplier engagement.
Quality Documentation: Create and update technical documents, quality reports, specifications, and standard operating procedures.
Collaboration with Development and Production Teams: Coordinate with development, engineering, production, and regulatory teams to ensure compliance with quality standards.
Failure investigations, PFMEA management, MRB committees, and more.

we are 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 Global Supplier Quality Engineer to join our team!
As a Global 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.