Medical Device Quality and Regulation PM JB-4143

A leading company specializing in quality and regulation processes for medical devices is looking for a Project Manager.

We lead processes with international companies, serial entrepreneurs, and are at the forefront of professional and academic work in the field.

The role is part of the company's management chain and includes multidisciplinary responsibility for all aspects of regulation: quality assurance, standardization, certification, international registration, clinical studies, and usability engineering.

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

Requirements:

• Relevant engineering degree - an advantage
• At least 10 years of experience as a quality and/or regulatory manager in a manufacturing equipment company - required
• Certification as an ISO13485 auditor - required
• Experience in leading a quality and regulatory area/managing employees in the field - required
• Passion for the field and a desire to develop and excel
• High level of written and oral expression in Hebrew and English
• High service awareness, excellent communication and ability to work with many interfaces