EMEA Regulatory Affairs Specialist (Medical Devices)

Intuitive seeks a Regulatory Affairs Specialist to provide advanced regulatory support for NPD, market expansion, and sustaining operations across EMEA. Must master EU MDR, ISO 13485, and RoHS, and lead regulatory submissions with cross-functional teams. The role requires collaboration with Product Lifecycle Management, Supply Chain, Marketing, and Commercial groups to align regulatory requirements with business goals. Strong project management and global regulatory knowledge are essential. J-1…