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.
We are looking for a QA Engineer to join our team! this is not a SW QA position
This is an ISRAELI BASED ON - SITE POSITION
Location: Netanya
BioProtect Ltd is a leading medical start up in radiation protection technology. We offer spacers protecting healthy tissue during radiation oncology treatments, based on proprietary biodegradable balloon technology. The balloons suit a wide range of clinical applications in the fields of oncology and general surgery. The company’s first product, the BioProtect Balloon Implant, protects healthy tissue in patients undergoing radiation therapy for prostate cancer.
The Opportunity
In this role, you will Oversee and assess the quality of manufacturing process
In This Position You Will Be Asked To
- Support in-house quality activities in production.
- Participate in non-conforming material processes, including investigations, MRB meetings, and implementation of corrective actions
- Support Change control process (ECO), including development and documentation of manufacturing work instructions, training, and change assessments.
- Data collection and analysis of trend (e.g., MRB, Yields).
- Review Device History Records for accuracy and completeness for product release.
- Support QC activities including in-coming, in-process and final inspection.
- Define quality requirements for production and process improvements.
- Relevant degree (e.g., biomedical, mechanical engineering or related science / technical discipline)
- 2 - 4 year of relevant experience in a similar role within a medical device company.
- CQE certification – an advantage
- Familiarity with medical device standards and regulations (MDR 2017/745, ISO 13485, FDA QSR, etc.).
- Knowledge of statistical techniques, risk analysis, root cause analysis, and process validation – an advantage.
- Ability to work under pressure to meet schedules and deadlines within quality and regulatory standards
- Strong analytical, problem-solving, and communication skills.
- Excellent English language skills (verbal and writing)
- Experience with Class III implantable medical devices
- Experience with working in controlled environment (clean room)
Requirements
Bonus Points:
- Experience with Class III implantable medical devices
- Experience with working in controlled environment (clean room)
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