Regulatory/Clinical Affairs Specialist
By GSI At Sandy Springs, GA, United States
Maintain knowledge of current regulatory requirements and standards, and communicate changes to relevant stakeholders.
Knowledge of FDA regulations and international regulatory requirements
Offering a highly competitive salary, comprehensive benefits package, and opportunities for growth and advancement within the company.
4 + years of experience in regulatory affairs within the medical device industry.
Experience with registration and commercialization of medical devices
Strong analytical, problem-solving, and decision-making skills.