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 Manager to join our team!
Location: Tzur Yigal/ 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 support manufacturing and operation with establishment and overall responsibility of Change Control processes.
In this position you will be asked to:
• Review and approve qualification and validation plans, protocols, and reports for compliance with the requirements, and the applicable regulations.
• Maintain the QMS to fulfill quality and regulatory requirements:
o Authors new or revised site procedures as assigned.
o Assures compliance of local QMS procedure and updates as required.
o Maintains the effectiveness of the QMS in accordance with the company objectives and applicable requirements
• Executes QA activities in line with defined procedures and processes: CAPA non-conformities, training, document control
• Ensures that all suppliers used by the company are selected, evaluated and re-evaluated and that records of this assessment are maintained.
• Ensures quality records are established and maintained to provide evidence of the QMS effectiveness.
• Review, edit and approve change controls, work-instructions, and other documentation.
A successful candidate will have the following qualifications:
• 4-5 years’ related experience in a medical device company
• Experience and knowledge with standards and regulations (MDR 2017/745, ISO 13485, FDA QSR)
• Experience with validation documentation review
• Experience with statistical techniques, risk analysis
• Excellent English language skills (verbal and writing)
• Relevant degree (e.g., biomedical engineering or related science / technical discipline)
Bonus Points:
• Experience with Class III implantable medical devices
• Experience with working in controlled environment (clean room)
BioProtect is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, colour, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
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.
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