דרושים » אבטחת איכות QA » NPI Quality Engineer

we are looking for a NPI Quality Engineer.
Key Responsibilities:
Coordinate Cross-Functional Teams: Collaborate with R&D, design, procurement, and production teams to ensure smooth product launches.
Process Development: Develop and optimize manufacturing processes for new products using quality tools.
Documentation: Review and maintain process documentation, work instructions, and operator training materials.
Prototype Builds: Support PT builds and production ramp-up activities, ensuring product quality, yield, and cycle times meet expectations.
Issue Resolution: Identify and resolve production issues during development and transfer phases.
Compliance: Ensure compliance with quality and regulatory standards.
Continuous Improvement: Implement continuous improvement practices to enhance production efficiency and product quality.

Review of Contract ,Customer SOW and SPEC requirements to ensure compliance of design and production.
Approve gates review at R&D
PLCM (Project Life Cycle Management) - process control, full partnership in project management during the development, testing, production, customer delivery and customer support phases throughout the product life
Identifying regulatory Gaps in new and carrent projects
Perform Internal and External Audits
QA presence in R&D process (capacity) and ability to prevent errors in design
Follow up after R&D corrective and preventive actions and Improvement Plans
Transfer products from development to NPI and serial production (QA activities)
Review and approval ECO / MCO / ATP/ATR, Waiver relate to R&D , ENG
Writing QA procedures
FRACAS Management
Quality Assurance Program Plan (QAPP) and the Quality Allocation Tasks for the program.
Customer complince - relate to NPI , Pre production , design errors
Perform Quarterly data analysis for QBR

Required Senior NPI to Mass Production Engineer
As an NPI to Mass production Engineer, you'll work in a fast-paced multi-disciplinary group, highly involved on products engineering design from early stages, develop and qualify solutions in a manufacturing environment, including review and support our global CEM production capabilities, quality, and readiness to Mass production. Ensure excellent standards of manufacturability, yield improvement, and advanced process controls. Collaborate with our greatest teams to maintain strong functional relationship to meet our team requirements and delivery schedules (SOL).
What you'll be doing:
Lead products transition from NPI to MP. Assure products are at highest quality, capacity and material availability readiness when moving to MP. Find opportunities for potential processes improvements and collaborate with multi-functional teams to implement.
You will be working concurrently with our phenomenal NPI and engineering teams on production processes, products design, and readiness to MP.
Working with our worldwide CEMs to ensure excellent standards of manufacturability. Assure CEM production capabilities and readiness on early product stages driven by company forecast requirements. Assure CM high performance execution for products under our team responsibility.
Be our excellent team key part of new products designs and processes. Represent mass production requirements and contract manufacture capabilities.

We are looking for an experienced Pre-Silicon Quality Manager to lead quality initiatives across our R&D organization, working closely with chip design, verification, and Application Engineering teams.
In this role you will be focused on engineering quality across the pre-silicon development lifecycle, ensuring robust development processes, strong verification practices, and continuous improvement. The ideal candidate combines technical experience in RTL / chip design environments with the ability to partner with engineering teams, influence stakeholders, and promote a strong quality culture across the organization.
Responsibilities:
Lead quality initiatives across the pre-silicon development lifecycle
Define and implement quality gates and release criteria for chip development milestones
Promote a shift-left approach to improve early defect detection during design and verification
Define, implement, and improve engineering quality processes and development frameworks
Lead escape analysis, root cause investigations, and lessons learned to prevent recurrence of issues
Define and track quality KPIs, engineering metrics, and dashboards to support data-driven decision making
Perform defect analytics and trend analysis to identify systemic issues and improvement opportunities
Manage corrective and preventive actions (CAPA) and monitor effectiveness of implemented actions
Improve development, verification, and release processes across engineering teams
Identify and manage engineering quality risks throughout the development lifecycle
Drive cross-organizational continuous improvement initiatives across engineering teams
Partner with RTL design, verification, and Application Engineering teams to strengthen product quality and reliability
Support and improve quality processes that enable smooth customer onboarding, efficient integration, and reliable use of the Pre-Silicon solution
Improve issue management processes and feedback loops between engineering, AE, and customer-facing teams
Promote quality culture and engineering best practices across the organization.

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

We are a Sisram Medical company, is a global leader in medical-aesthetic technologies, with over 25 years of experience in energy-based devices (EBD). Over the years, we have evolved into an integrated aesthetic and wellness ecosystem that combines medical devices, injectables, diagnostics, and personalized skincare. The company operates in a dynamic, innovation-driven environment, merging advanced technology with deep clinical understanding to create holistic solutions for aesthetic clinics.
 Our headquarters are in Caesarea, Israel, with business operations in more than 100 countries worldwide. Operations Quality Leadership
* Lead, mentor, and professionally develop the Operations Quality Team.
* Set quality standards, inspection controls, and defectprevention methodologies on the production floor. MRB, NC & CAPA Management
* Lead MRB decision-making and material disposition.
* Own NC/CAPA processes: investigation quality, rootcause analysis, corrective & preventive action closure. Quality Systems & Compliance
* Maintain and improve SOPs, work instructions, and quality procedures related to operations.
* Own risk assessments (pFMEA), risk surveys, and operational quality KPIs. Support for External Audits
* Act as a key operational quality representative during Notified Body, MDSAP, ISO 13485, FDA, and customer audits.
* Ensure operational readiness: documentation integrity, calibration status, inspection records, training, material traceability, and MRB completeness.
* Drive audit response actions, containment, and long-term corrective actions in coordination with RA/ QA. Supplier Quality & Supplier Audits
* Lead supplier quality oversight with Supply Chain.
* Conduct supplier qualification and performance audits (ISO 9001/13485-based).
* Manage supplier NCs, SCARs, incoming defects, and continuous improvement activities.
* Align incoming inspection plans with supplier capability and risk level. Complaint Investigation Support
* Partner with Global Service for field complaint investigations, ensuring fast and accurate operational rootcause analysis and corrective actions. Operational Excellence & Projects Lead quality improvement initiatives, yield enhancement, process stabilization, etc

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

Required Product Quality Manager
The Product Quality Manager is a critical role in the quality management in the space industry. In this position, youll work closely with all Engineering teams, and with Product, Program Management and Operations teams, contributing directly to our ongoing projects and initiatives.
Job Description:
Lead end-to-end quality activities across the program lifecycle, including:
Program audits
Involvement and support in internal and external project reviews and milestones
Preparation of relevant documentations and deliverables to the customer according to milestones, and customers requirements
Management of program nonconformities, alerts, and corrective actions
Support of the risk management, in coordination with the Project Management and Engineering\operations functions
Program KPIs monitoring
Support to the documentation and data control, quality records, and configuration management
Interface with customers and all stakeholders regarding program quality activities
Support operations and supply chain activities related to quality aspects, such as incoming inspection, nonconformities, and production support
Ensure program compliance with applicable space industry standards and our quality specifications.

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 an experienced Global Manufacturing Program Manager to join our team. This role involves managing complex programs from planning through full implementation, including knowledge transfer, production infrastructure setup, and compliance with regulatory and logistical requirements.
* Lead complex programs for establishing manufacturing and maintenance sites abroad, from planning to full execution.
* Drive knowledge transfer processes to international teams.
* Establish and implement production lines, processes, and operational procedures.
* Collaborate with cross-functional teams, including Engineering, Operations, Procurement, Logistics, and international stakeholders.
* Manage local and international suppliers and subcontractors.
* Ensure compliance with quality standards, regulatory requirements, and security protocols.
* Oversee project timelines, budgets, and risk management.