Project Manager in Quality and Regulation JB-4143

For a leading company specializing in quality and regulatory processes of medical devices, a Project Manager is required.

We lead processes with international companies, serial entrepreneurs, and are at the forefront of professional and academic activity 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 to manage projects and consultants at a high level in the fields of quality and regulation, while meeting professional and financial targets.

Relevant engineering degree – an advantage

At least 10 years of experience as a Quality and/or Regulatory Manager in a manufacturing medical device company – mandatory

Certification as an ISO 13485 auditor – mandatory

Experience in leading quality and regulatory functions / managing employees in the field – mandatory

Passion for the field and desire to develop and excel

High-level written and verbal expression in Hebrew and English

High service orientation, excellent communication, and ability to work with multiple interfaces