Global Regulatory Specialist

The Regulatory Affairs group is responsible for the global regulatory strategy, including global product registrations, maintenance and continued product compliance to enable bringing innovative products and solutions to market. This role will provide regulatory subject matter expertise and support for the global medical device/diagnostic portfolio within Women's Health business unit. The Global Regulatory Specialist will be responsible for the execution of regulatory strategies and activities to support the development, registration, launch and maintenance of Women's Health products. This will include providing regulatory intelligence, strategy, and support for global product registrations and compliance, as well as supporting product development and lifecycle management activities. The ideal candidate will have demonstrated experience in regulatory affairs within a medical device/diagnostic organization, strong regulatory affairs technical knowledge, and the ability to work effectively across global teams.

GE HealthCare is a leading global medical technology, pharmaceutical diagnostics, and digital solutions innovator. GE HealthCare helps clinicians deliver better healthcare to their patients by enabling earlier diagnosis, more targeted therapy, and improved monitoring. GE HealthCare is dedicated to advancing medical care and improving patient outcomes. We are a trusted partner in providing comprehensive, integrated solutions that enable clinicians to make faster, more informed decisions. GE HealthCare's broad expertise in medical imaging and information technologies, medical diagnostics, patient monitoring systems, drug discovery, and biopharmaceutical manufacturing technologies is helping clinicians around the world deliver the best care and make a real difference in patient lives.