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We are looking for a hands-on NPI & Quality Engineer to own and lead New Product Introduction activities while ensuring product quality across production and deployment.
This role serves as a key bridge between R&D, Operations, QA, and Production, supporting smooth product launches and high operational standards, and requires on-site presence at the production facility.
Key Responsibilities
Lead NPI processes from development to production readiness
Own QA activities related to new and existing products
Be present at the production site to oversee and control quality operations and manufacturing activities
Act as the main interface between R&D and Operations
Manage and control NPI documentation and processes, including TN (Technical Notes), waivers, deviations, and ECO/ECRs
Support production, QA, and manufacturing ramp-up activities
Define, implement, and improve quality processes, inspections, and acceptance criteria
Identify risks, gaps, and process improvements during product introduction
Ensure full documentation, procedures, and handover are production-ready.

We are seeking a highly motivated and experienced Sr. Production and Quality Engineer to drive exceptional product quality, patient safety, and field reliability across the Installed Base (IB). This is a key technical role supporting production stability, RMA/DOA investigations, Automated Test Equipment (ATE) performance, and cross-functional quality engineering initiatives in a regulated medical device environment
Key Responsibilities
In this role, you will
Support RMA/DOA processes and continuous reduction of field failures.
Support qualifications and control of ATE testers in production lines.
Support ECO/ECR processes, NPI projects, product updates, and cross-functional engineering changes.
Work closely with R&D, engineering, manufacturing, and operations teams to enhance product quality and resolve technical issues.
Drive continuous improvement initiatives using tools such as Six Sigma, Lean, and Root Cause Analysis (RCA).
Participate in supplier selection and conduct suppliers audits.
Ensure compliance with ISO 13485, FDA 21 CFR 820, MDR, and other applicable medical device regulations.
Maintain and support quality documentation, including CAPA, Non-Conformance Reports (NCRs), and risk management documentation.

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 Production 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.
Monitor NCMR process including quality KPIs
Support for non-conformity investigations and assign effective corrective actions for NCMRs and ensure timely closure and documentation.
Perform / review Root Cause Analysis as part of NCMR process and assign relevant corrective actions.
Act as QA representative for Manufacturing Quality process
Conduct quality assurance activities such as data analysis and statistical evaluations, SOP review and approvals, audit preparation
Direct Manager: Manufacturing Quality Manager

We are looking for a hands-on Production Quality Control professional to take ownership of quality inspection activities across suppliers and production lines within our quality team.

This role combines supplier quality, incoming inspection, in-process and final inspections, and requires broad quality expertise. The position involves close collaboration with internal and external stakeholders, including periodic travel to suppliers in Israel and abroad.

What you will do:
Perform quality inspections across the full production lifecycle, including incoming, source (at supplier sites), in-process, and final inspections through shipment release.
Conduct supplier quality audits and assessments.
Work with manufacturing and suppliers in aerospace and defense production environments.
Apply quality standards, procedures, and sampling plans to determine product acceptance or rejection.
Review quantities, determine sample sizes, and make quality decisions using established inspection methodologies.
Prepare clear, professional-quality reports and inspection documentation.
Work closely with multiple stakeholders: suppliers, production, engineering, and quality.
Travel to suppliers in Israel and abroad as needed.

we are 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 Production 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.
* Monitor NCMR process including quality KPIs
* Support for non-conformity investigations and assign effective corrective actions for NCMRs and ensure timely closure and documentation.
* Perform / review Root Cause Analysis as part of NCMR process and assign relevant corrective actions.
* Act as QA representative for Manufacturing Quality process
* Conduct Quality Assurance activities such as data analysis and statistical evaluations, SOP review and approvals, audit preparation Direct Manager: Manufacturing Quality Manager

Were looking for an experienced R&D Quality Engineer who doesnt just audit processes, but actively partners with engineering teams to build better products.
In this role, youll play a key part in strengthening our Automotive SPICE maturity while ensuring that quality is embedded into how we design, develop, and deliver cutting-edge automotive systems.
If you enjoy working hands-on with development teams, influencing engineering practices, and turning process frameworks into real-world impact, this role is for you.
What will your job look like:
Partner with system and software engineering teams to implement and improve ASPICE-compliant processes.
Drive continuous improvement of product quality, not just process adherence
Support and guide teams through ASPICE assessments (internal & external)
Translate ASPICE requirements into practical, scalable engineering workflows
Identify gaps, risks, and improvement opportunities across the development lifecycle
Coach teams on best practices in systems & software engineering
Contribute to building a quality-driven engineering culture.

We are seeking a Quality Engineer to ensure product and process quality across manufacturing, suppliers, and new product introduction activities. The role supports and maintains the Quality Management System, ensures compliance with applicable standards, and implements effective quality controls throughout the product lifecycle. The Quality Engineer leads root cause analysis and corrective actions, works closely with cross-functional teams, and drives continuous improvement to enhance quality performance and customer satisfaction.
Key Responsibilities:
Support and maintain the Quality Management System (QMS) in compliance with ISO 9001 and applicable standards
Lead investigations of nonconformances, deviations, and customer issues, including root cause analysis and CAPA
Define and support inspection plans, acceptance criteria, and quality controls across manufacturing
Participate in New Product Introduction (NPI) activities, including design reviews, FMEA, pilot builds, and FAI
Support supplier quality activities, including issue resolution, corrective actions, and performance monitoring
Conduct and support internal and supplier audits and ensure timely closure of findings
Analyze quality data and KPIs to identify trends and drive continuous improvement initiatives
Collaborate with Engineering, Operations, Supply Chain, and other stakeholders to ensure quality objectives are met