Medical Device Regulation Manager JB-4143

A company specializing in medical device quality and regulatory processes requires a Quality and Regulatory Manager.

The company is a leader in its field and serves 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 that provides the best response to all aspects of regulation, including quality assurance, standardization, certification, international registration, clinical studies, and usability engineering.

The purpose of the position is to create value for the customer and manage a high-level project in the fields of quality and regulation while meeting professional and financial goals.

Requirements:

• Engineering degree - an advantage
• At least 10 years of experience as a quality and/or regulatory manager in a manufacturing equipment company - mandatory
• Certification as an ISO13485 auditor - mandatory
• Passion for the field and a desire to develop and excel
• Ability to express oneself in writing And fluent in Hebrew and English at a high level
• High service awareness, excellent communication and ability to work with many interfaces
• Willingness to work in the Sharon area and travel to client offices from time to time