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