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.
ג'ובאינפו בע"מ
- חיפה
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ג'ובאינפו בע"מ
- חיפה
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מלאה
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As the QA Doc Control Specialist, you will be responsible for all aspects of document control according to established procedures. In addition, you will assist the QA Manager in controlling and managing the quality management system via internal auditing, CAPA and complaints handling, preparation of periodical data analysis, management reviews, control of non-conformance, and control of changes.
Support and active involvement in improving the company's QMS and internal quality process.
Open and handle CAPA, including identifying the cause, root cause, correction, and corrective actions.
Responsible for the company's employee Training on QA aspects.
Cooperating in the setting of quality objectives in the company processes.
Ensure the company's quality system procedures and products comply with regulatory guidelines and external standards.
Performing data Analysis.
Support and active involvement in improving the company's QMS and internal quality process.
Open and handle CAPA, including identifying the cause, root cause, correction, and corrective actions.
Responsible for the company's employee Training on QA aspects.
Cooperating in the setting of quality objectives in the company processes.
Ensure the company's quality system procedures and products comply with regulatory guidelines and external standards.
Performing data Analysis.
Requirements:
2+ years of hands-on experience in a Quality Assurance department in the Medical Device industry.
Familiarization with ISO 13485:2016 requirements and interpretation of the Standard to practical and regulatory-complying processes and procedures.
Knowledge in Design Control deliverables, change control process, and risk management methods - An advantage.
Experience with quality management systems interactions and external NB audits - An advantage.
A Bachelors degree in a technical or scientific discipline is an advantage.
2+ years of hands-on experience in a Quality Assurance department in the Medical Device industry.
Familiarization with ISO 13485:2016 requirements and interpretation of the Standard to practical and regulatory-complying processes and procedures.
Knowledge in Design Control deliverables, change control process, and risk management methods - An advantage.
Experience with quality management systems interactions and external NB audits - An advantage.
A Bachelors degree in a technical or scientific discipline is an advantage.
This position is open to all candidates.
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.
פתח תקווה
אונליין
אונליין
תעודה ממשלתית
2 חודשים
סבסוד
