Global Regulatory Lead, Medical Devices

A medical consulting firm in Texas is seeking a Regulatory Affairs Level III (Senior Specialist) to oversee global product registrations and compliance for medical devices. The ideal candidate will have 5-7 years of experience in regulatory affairs within the medical device industry, particularly with respiratory devices, and will be responsible for ensuring adherence to regulatory standards and providing input throughout the product lifecycle. Strong analytical and communication skills are essential. This role offers a dynamic environment with opportunities for professional growth. #J-18808-Ljbffr