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.
מלאה
לחברה בהוד השרון
We are looking for a motivated and experienced QA Coordinator to join our team!
As a QA Coordinator, you will assist in maintenance of QA system and document control
according to internal and external regulatory requirements
Key Responsibilities:
Provide Quality Support within the organization under quality system
requirements of ISO 13485, FDA regulation and MDR 2017-745.
Manage document control system and training records.
Review DMR documents and provide inputs related to QA and update SOPs, as
needed.
Provide trainings within the organization.
Manage the approval, evaluation and monitoring of suppliers system.
Review engineering change orders, validation protocols and reports.
Review incoming inspection records and manufacturing records (DHR) as part of
the batch release approval process.
Handling and writing of non-conforming and CAPAs.
Assist in preparation for audits.
Review calibration records.
Support additional quality and regulatory activities as assigned by Director of QA &RA.
We are looking for a motivated and experienced QA Coordinator to join our team!
As a QA Coordinator, you will assist in maintenance of QA system and document control
according to internal and external regulatory requirements
Key Responsibilities:
Provide Quality Support within the organization under quality system
requirements of ISO 13485, FDA regulation and MDR 2017-745.
Manage document control system and training records.
Review DMR documents and provide inputs related to QA and update SOPs, as
needed.
Provide trainings within the organization.
Manage the approval, evaluation and monitoring of suppliers system.
Review engineering change orders, validation protocols and reports.
Review incoming inspection records and manufacturing records (DHR) as part of
the batch release approval process.
Handling and writing of non-conforming and CAPAs.
Assist in preparation for audits.
Review calibration records.
Support additional quality and regulatory activities as assigned by Director of QA &RA.
Requirements:
Qualification and required experience:
Bachelors degree in Engineering, science, technical discipline or equivalent field.
At least 2-3 years in QA role within the medical device industry.
Familiarity with medical device regulations, including ISO 13485, MDR and FDA
regulations.
Excellent written skills in English.
Excellent communication skills.
Strong organizational and time management skills with the ability to prioritize
tasks.
Ability to work independently and as part of a team.
Qualification and required experience:
Bachelors degree in Engineering, science, technical discipline or equivalent field.
At least 2-3 years in QA role within the medical device industry.
Familiarity with medical device regulations, including ISO 13485, MDR and FDA
regulations.
Excellent written skills in English.
Excellent communication skills.
Strong organizational and time management skills with the ability to prioritize
tasks.
Ability to work independently and as part of a team.
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.
בני ברק
אונליין
אונליין
תעודה ממשלתית
2 חודשים
סבסוד
