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.

מעוף ביוטק

נתניה

מעוף ביוטק

נתניה
מלאה

הזדמנות להשתלב בחברת ביוטק מצליחה!!
In this position you will be asked to:
Maintain the QMS to fulfill quality and regulatory requirements:
Authors new or revised site procedures as assigned.
Assures compliance of local QMS procedure and updates as required.
Maintains the effectiveness of the QMS in accordance with the company objectives and applicable requirements
Executes QA activities in line with defined procedures and processes: CAPA non-conformities, training, document control
Ensures that all suppliers used by the company are selected, evaluated and re-evaluated and that records of this assessment are maintained.
Ensures quality records are established and maintained to provide evidence of the QMS effectiveness.
Review, edit and approve change controls, work-instructions, reports and other documentation.

Requirements:
A successful candidate will have the following qualifications:
4-5 years related experience in a medical device company
Experience and knowledge with standards and regulations (MDR 2017/745, ISO 13485, FDA QSR)
Experience with statistical techniques, risk analysis
Excellent English language skills (verbal and writing)
Relevant degree (e.g., biomedical engineering or related science / technical discipline)

Bonus Points:

CQE and process validation knowledge
Experience with Class III implantable medical devices
Experience with working in controlled environment (clean room)

This position is open to all candidates.