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
For a fast-growing medical device company focused on developing, manufacturing,
and selling innovative devices for endovascular interventional procedures
We are seeking a skilled and detail-oriented QA Engineer to join our team
Quality Engineer Scope & Responsibilities:
Manage ECOs including risk assessment, DMR updates and validation activities (IQ/OQ/PQ)
Handle DCOs in PLM system and update QA procedures
Lead NCR/CAPA processes to ensure effective resolution
Support production with quality oversight and deviation management
Address quality issues in a timely manner
Participate in regulatory audits (FDA, ISO 13485, EU MDR, MDSAP)
LOCATION: Yokneam
and selling innovative devices for endovascular interventional procedures
We are seeking a skilled and detail-oriented QA Engineer to join our team
Quality Engineer Scope & Responsibilities:
Manage ECOs including risk assessment, DMR updates and validation activities (IQ/OQ/PQ)
Handle DCOs in PLM system and update QA procedures
Lead NCR/CAPA processes to ensure effective resolution
Support production with quality oversight and deviation management
Address quality issues in a timely manner
Participate in regulatory audits (FDA, ISO 13485, EU MDR, MDSAP)
LOCATION: Yokneam
Requirements:
Bachelor of Science degree or Engineering.
2-5 years of experience in medical device QA (ISO 13485, FDA QSR 820).
Internal auditor certification- an advantage
Ability to work in dynamic and multi-interfaced surroundings, micro and macro vision.
Strong attention to details and Self-learning ability.
Ability to manage time and priorities and work under pressure.
English - high level (both written and spoken).
Excellent leadership and people management skills.
Service oriented.
Knowledge and practical experience in Priority An advantage.
Bachelor of Science degree or Engineering.
2-5 years of experience in medical device QA (ISO 13485, FDA QSR 820).
Internal auditor certification- an advantage
Ability to work in dynamic and multi-interfaced surroundings, micro and macro vision.
Strong attention to details and Self-learning ability.
Ability to manage time and priorities and work under pressure.
English - high level (both written and spoken).
Excellent leadership and people management skills.
Service oriented.
Knowledge and practical experience in Priority 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.
הרצליה
ערב
3 חודשים
הרצליה
