Our client is looking for a Regulatory Consultant for a 3 month project. This individual will be responsible for change orders and international registrations. The client is working on ventilation devices and has many things currently going on including but not limited to bringing a new product to market, software changes, international registrations, sustaining work, etc. These are all class 2 devices with software as a component. This resource will need to have hands on experience with software that is on medical devices. If this resource has experience with the software updates/changes that are required for EU MDR that would be a huge plus.
Remote: Regulatory Consultant (229831)