Incoming Inspection & MRB Coordinator at ZOLL Medical Corporation

Caesarea, Haifa District, Israel -

Full Time

Start Date

Immediate

Expiry Date

16 May, 26

Salary

0.0

Posted On

15 Feb, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Incoming Inspection, MRB Coordination, Workflow Coordination, Cross-Functional Liaison, Testing, Material Review Board (MRB), Supplier Communication, ERP Systems, KPI Accountability, Sampling Plans (AQL), Technical Drawings, Precision Measuring Tools, Quality Decisions, Team Leadership, ISO 13485, FDA 21 CFR Part 820

Industry

Medical Equipment Manufacturing

Description

Itamar At ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients suffering from serious cardiopulmonary and respiratory conditions. ZOLL Itamar is an innovative medical device technology company that focuses on the development and manufacturing of Home Sleep Apnea Tests to aid in the diagnosis of respiratory sleep disorders. Our core product is the WatchPAT®️ family, a revolutionary FDA-cleared portable home sleep apnea test device, that is based on proprietary signal and analysis. 80% of patients who have sleep apnea are undiagnosed. We are committed to reach those undiagnosed patients and provide testing to promote wellness and enhance overall quality of life. WatchPAT®️ is commercially available within major markets including the U.S., Japan, and Europe, and is the leading home sleep apnea test in the US. ZOLL Itamar's corporate headquarters, research and development and manufacturing are located in Israel with U.S. headquarters based in Atlanta, GA. Job Type On Site Job Summary The Incoming Inspection & MRB Coordinator at ZOLL Itamar plays a pivotal role in ensuring the seamless flow of high-quality components for the WatchPAT family. In this position, you will be the central point of contact for operational quality, synchronizing activities between the warehouse, engineering, and external suppliers to maintain our rigorous FDA and ISO standards. Essential Functions Workflow coordinator: Define and manage daily priorities for incoming inspection to ensure alignment with production schedules. Cross-Functional Bridge: Act as the primary liaison between Quality, Supply Chain, and Suppliers to resolve quality issues and streamline material approval. Testing: conduct Inspection of the incoming good shipment according to Drawings and Specification. MRB: Oversee the Material Review Board (MRB) process, ensuring timely disposition of non-conforming materials and driving closure of open items. Suppliers: Communicate with key suppliers, including visits at supplier when needed ERP Responsibility: Perform all inventory and quality transactions accurately within the company’s ERP system. KPI Accountability: Ensure the department meets established targets for inspection turnaround time and accuracy. Supplier visits Required/Preferred Education and Experience Practical Engineer, certified Technician or a related technical field. required Certified Quality Auditor (CQA) or Certified Quality Inspector (CQI) or other Quality Certifications preferred knowledge of ISO 13485 and FDA 21 CFR Part 820. (QMSR) preferred At least 2-3 years of experience in Quality Control or Quality Assurance within a regulated industry (Medical Device, Pharma, Aerospace etc.) Knowledge, Skills and Abilities understanding of sampling plans (e.g., AQL), technical drawings, and the use of precision measuring tools. Hands-on experience working with ERP systems (e.g., SAP, Oracle, or Priority), PLM (Product lifecycle management). Ability to work independently, make firm quality decisions, and lead a team under pressure. Preferred Languages Hebrew - Expert English - Intermediate Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Standing - Constantly Walking - Constantly Sitting - Occasionally Lifting - Constantly Carrying - Constantly Pushing - Constantly Pulling - Constantly Talking - Occasionally Hearing - Frequently Repetitive Motions - Constantly Eye/Hand/Foot Coordination - Constantly Working Conditions Extreme cold - Occasionally Extreme heat - Occasionally Humidity - Occasionally Wet - Occasionally Noise - Frequently ZOLL is a fast-growing company that operates in more than 140 countries around the world. Our employees are inspired by a commitment to make a difference in patients' lives, and our culture values innovation, self-motivation and an entrepreneurial spirit. Join us in our efforts to improve outcomes for underserved patients suffering from critical cardiopulmonary conditions and help save more lives. ZOLL Medical Corporation, an Asahi Kasei Group Company, develops and markets medical devices and software solutions that help advance emergency care and save lives, while increasing clinical and operational efficiencies. With products for defibrillation and monitoring, circulation and CPR feedback, data management, therapeutic temperature management, and ventilation, ZOLL provides a comprehensive set of technologies that help clinicians, EMS and fire professionals, and lay rescuers treat victims needing resuscitation and acute critical care. For more information, visit www.zoll.com. The Asahi Kasei Group is a diversified group of companies led by holding company Asahi Kasei Corp., with operations in the material, homes, and health care business sectors. Its health care operations include devices and systems for acute critical care, dialysis, therapeutic apheresis, transfusion, and manufacture of biotherapeutics, as well as pharmaceuticals and diagnostic reagents. With more than 30,000 employees around the world, the Asahi Kasei Group serves customers in more than 100 countries. For more information, visit www.asahi-kasei.co.jp/asahi/en/.

Responsibilities

This role coordinates the daily priorities for incoming inspection, acting as the central liaison between the warehouse, engineering, suppliers, and Quality to ensure high-quality component flow for the WatchPAT family devices. Key duties include conducting inspections, overseeing the Material Review Board (MRB) process for non-conforming materials, and managing all related ERP transactions.