Global Regulatory Affairs Specialist, Medical Devices

A leading medical device company is seeking a Regulatory Affairs Specialist in Kennesaw, Georgia. The specialist will be responsible for supporting manufacturing, maintaining regulatory compliance, and managing regulatory submissions for FDA Class II or III devices. Ideal candidates will possess a Bachelor's degree and at least 2 years of relevant regulatory experience. Strong analytical and communication skills are essential. This role offers a chance to engage in cross-functional teamwork and contribute to the ongoing success of the company's innovative medical solutions. #J-18808-Ljbffr