Quality and Regulation Project Manager JB-4143

A company specializing in quality processes and regulatory affairs for medical devices is seeking a Project Manager. The company is a leader in its field, serving international companies, serial entrepreneurs, and is at the forefront of professional and academic work in the field. The position is part of a multidisciplinary team providing optimal solutions for all aspects of regulation including quality assurance, standards compliance, documentation, international registration, clinical studies, and usability engineering. The goal of the position is to create value for the client and manage a project at a high level in the fields of quality and regulatory affairs while meeting professional and financial objectives. Requirements: • Engineering degree - an advantage. • Certification as an ISO13485 auditor - mandatory • At least 10 years of experience as a Quality and/or Regulatory Manager in a medical device manufacturing company - mandatory. • Passion for the field and desire to develop and excel. • High level of written and verbal expression in Hebrew and English. • High service awareness, excellent communication skills, and ability to work with multiple interfaces.