Job requirements and application form

• Overall responsibility for the Quality Management System, including ownership and leadership of QMS processes such as CAPA, Complaints, Document Control, Training, Internal and External Audits, and Supplier Quality • Lead, maintain, and continuously improve the QMS to ensure compliance with applicable regulatory and quality standards • Manage and develop QMS processes and procedures, ensuring effective implementation across the organization • Monitor and assess QMS performance, identify gaps and improvement opportunities, and drive corrective and preventive actions • Prepare and present QMS-related data and metrics for Management Review and quality forums • Lead internal audits and support external and regulatory audits • Provide professional guidance, training, and support to stakeholders on QMS-related topics

• Bachelor’s degree in Engineering, Life Sciences, or a related field • 5-10 years of experience in Quality Assurance within the medical device industry • Proven experience in leading and managing a Quality Management System in a regulated environment • Strong knowledge of QMS processes, including document control, audits, CAPA, and training • Experience working with cross-functional teams and leading quality activities at an organizational level • Highly organized, detail-oriented, and able to manage multiple priorities • Strong verbal and written communication skills in English • Strong interpersonal skills and ability to influence, collaborate, and lead professionally Location: Sharon region