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

הרצליה

QHR

הרצליה
מלאה

Duties Essential job Functions:
a.Perform the following QA activities
i.Manage the incoming inspection process and the company control system
ii.Coordinate the following processes: approved suppliers, lot release, change control (ECO), nonconforming product (NCR), complaint handling, verification and validation (V V) testing activities including preparation of protocols and reports and TEST execution
iii.Maintain Design History File (DHF), Device Master Record (DMR) and QMS SOPs
b.Support the following QA activities: risk management, corrective and preventive action (CAPA), internal and external audits
C.Support the following Operations activities:
i.Purchasing, shipments, warehouse and office management

Requirements:
a.Practical engineering degree or equivalent technical certification, or
Bachelors degree in engineering or scientific discipline - an advantage
C.At least 3-5 years work experience in a medical device QA role working under an ISO 13485 certified QMS
d.Excellent communication, organizational and recordkeeping skills
e.Strong English technical writing skills, most of the work is in English
f.Must be fluent with MS Office in particular Excell
g.Must be able to work in a fast-paced environment with demonstrated ability to juggle multiple competing tasks and demands
h.Must be able to work in multi-disciplinary teams
i.Must be a team player
j.Experience with clean room manufacturing - an advantage
k.Experience with V V testing - an advantage

This position is open to all candidates.