Medical quality assurance

Responsibilities:

• Support and maintain Quality Management System (QMS) processes in accordance with applicable regulations and standards.
• Contribute to quality activities across the product lifecycle, including development and manufacturing-related processes.
• Participate in the preparation, review, and maintenance of quality documentation such as procedures and work instructions.
• Collaborate with cross-functional teams to support quality objectives and continuous improvement.
• Support compliance with regulatory and quality standards, including ISO 13485.
• Participate in internal and external audits as needed.

Requirements

• 5+ years of experience in Quality Assurance within the medical device industry.
• BSc in a relevant scientific or engineering discipline.
• Familiarity with medical device quality processes (e.g., risk management, design controls, manufacturing-related quality activities).
• Strong written and verbal communication skills in English; Hebrew is an advantage.
• High attention to detail and strong organizational skills.
• Ability to work both independently and as part of a team in a dynamic environment.