In this role, you will support the implementation and maintenance of our Quality Management System (QMS), ensuring compliance with regulatory standards such as ISO 13485 and 21 CFR Part 820. You will work closely with cross-functional teams to help maintain quality processes, conduct inspections and contribute to continuous improvement initiatives.
This is an excellent opportunity to gain hands-on experience in a fast-paced, innovative startup environment while working on medical devices that make a real difference in patients' lives.
• Bachelor’s degree in engineering, biotechnology, chemistry, or a related field (or equivalent relevant experience).
• 1-3 years of experience in a medical device QA role.
• Basic knowledge of ISO 13485, 21 CFR Part 820, or quality systems in regulated
industries.
• Strong attention to detail, problem-solving skills, and a willingness to learn.
• Excellent written and verbal communication skills in English.
• Ability to work collaboratively in a team environment.
* משרה זו פונה לנשים וגברים כאחד.