Careers that Change Lives
Mazor Robotics Ltd, a Medtronic company since December 2018, is a global pioneer in the field of spine robotics. We have a multi-disciplinary team developed on products that combine innovative 3D surgical planning and analytics with cutting edge robotic solutions/products. Join us in working at a local and friendly site with global impact and reach.

A Day in the Life
Support the different regulatory activities:
· Regulatory assessments and registrations worldwide
· Review promotional material and labeling for regulatory compliance.
· Write, update and maintain technical files for Class I and Class IIa.
· Support global regulatory requirements and submissions.
· Regulatory assessment of changes.

Note: The following are meant to be representative but not necessarily all inclusive of the duties and responsibilities for this position title.

Must Have
· A degree in a related scientific or engineering discipline
· Minimum of 2 years of related experience in regulatory affairs (Medical device or pharmaceutical industry)
· Fluent in Hebrew and English (verbal and written communication skills)


Nice to Have
Experience in the medical device industry- Significient Advantage
Advanced degree in a related scientific or engineering discipline
Knowledge of medical device regulations and standards, especially US (FDA) and EU (MDD/MDR) related