The Quality and Regulatory Affairs Specialist is responsible of the product
registration in different markets in accordance with the local legal
requirements. He is also the main contact between the organization and
authorities to ensure reliable forward of information.
Special expertise
* Microsoft Excel
* SAP
* Knowledge of ISO 9001, ISO 13485 and Medical Device Directive is a plus
* Knowledge of national medical device regulations
Languages
* Fluency in English and Arabic, both spoken & written.
* French is a plus
* Personal skills requirements
* Solid problem solving skills
* Ability to work independently and under pressure
* Organizational, follow up and time management skills
Education
* Bachelor's Degree in Engineering, Business or Political Science.
Professional experience
* 3 to 5 years of experience in registration activities and/or quality assurance with preference to international medical device regulations.
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