עדיין מחפשים עבודה במנועי חיפוש? הגיע הזמן להשתדרג!

במקום לעבור לבד על אלפי מודעות, Jobify מנתחת את קורות החיים שלך ומציגה לך רק משרות שבאמת מתאימות לך.

מעל 80,000 משרות • 4,000 חדשות ביום
חינם. בלי פרסומות. בלי אותיות קטנות.

QHR

מספר מקומות

QHR

מספר מקומות
מלאה

?Responsible for product integration, reliability, qualification, environmental and safety tests in external LAB and in-house. Perform FTA and detecting preferred system technical solutions.
?Lead and maintain products configuration following procedural development of medical products (Design Control): Design History Files (DHF), Device Master Record (DMR), (RTM) Requirements Traceability Matrix and their change approval.
?Creating / reviewing maintenance wide range of Engineering ation (Assy WI, IQ/OQ/PQ,V V protocols, Acceptance Criteria, Procedures, Templates and Forms) with QA Operations Departments deep cooperation.
?Lead system aspects in products portfolio: top-level architecture, modern technologies implementation, define performance goals and tests, serviceability, interfaces specs, design to assembly and cost, human factors design, with reference to medical device standards

Requirements:
?B.Sc. or M.Sc. degree in Medical/Mechanical/ system Engineering.
?Knowledge in Cryogenics Preferred.
?2-5 years of proven experience in Engineering environments of multidisciplinary products or medical devices.
?Interpersonal skills and excellent teamwork - the ability to meet technical as well as human challenges.
?Experience in medical device quality systems, specifically Risk management file and Design Inputs.
?Experience resolving complex system issues and being hands on when needed.
?Good ation skills.
?Experience in MS-Office, MS-Project, MS Planner Must.
? Experience in Solid works, LabView, ERP, PLM, PDM tools Advantage.
?Fluent in Hebrew and English.

This position is open to all candidates.