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
A global medical device company located in Caesarea, specializing in the manufacturing of dental implants, is seeking a:
QA /RA Engineer (Design)
**This is a temporary position for 9 months with a real possibility for continuation.
Note: The company welcomes applications from recent graduates with a relevant bachelor's degree
Job Responsibilities:
- Lead quality control and Quality Assurance processes throughout the medical device product lifecycle
- Develop and execute comprehensive TEST plans to ensure compliance with regulatory and functional product requirements
- Plan and perform validations and development tests for products and processes, including writing/reviewing protocols and reports
- Write, update, and approve development files, technical documents, and work procedures in accordance with regulatory requirement
QA /RA Engineer (Design)
**This is a temporary position for 9 months with a real possibility for continuation.
Note: The company welcomes applications from recent graduates with a relevant bachelor's degree
Job Responsibilities:
- Lead quality control and Quality Assurance processes throughout the medical device product lifecycle
- Develop and execute comprehensive TEST plans to ensure compliance with regulatory and functional product requirements
- Plan and perform validations and development tests for products and processes, including writing/reviewing protocols and reports
- Write, update, and approve development files, technical documents, and work procedures in accordance with regulatory requirement
Requirements:
- Bachelor's degree in Life Sciences, Biomedical Engineering, Mechanical Engineering, Biotechnology, Chemistry, Materials Engineering, or similar field - mandatory
- Preferably about one year of experience in the medical device industry, with emphasis on QA and regulatory processes - advantage
- Knowledge of FDA CFR 820 requirements, ISO 13485 standards, and CE requirements for medical product development - advantage
- Experience in performing validations and quality tests for medical products - advantage
- High level of English proficiency (reading and writing technical and engineering documents)
- Ability to work with interfaces and excellent communication with various departments in the organization
- Bachelor's degree in Life Sciences, Biomedical Engineering, Mechanical Engineering, Biotechnology, Chemistry, Materials Engineering, or similar field - mandatory
- Preferably about one year of experience in the medical device industry, with emphasis on QA and regulatory processes - advantage
- Knowledge of FDA CFR 820 requirements, ISO 13485 standards, and CE requirements for medical product development - advantage
- Experience in performing validations and quality tests for medical products - advantage
- High level of English proficiency (reading and writing technical and engineering documents)
- Ability to work with interfaces and excellent communication with various departments in the organization
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.
ערב
36 חודשים
תעודה ממשלתית
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