Global Regulatory Affairs Associate II: Device Submissions

A global medical device company is seeking a Regulatory Affairs Specialist to provide regulatory support and guidance for device product registrations. The role involves planning registration packages, evaluating changes for regulatory impact, and ensuring compliance with regulations. Ideal candidates will have a bachelor's degree in a relevant field and a minimum of two years of experience in regulatory affairs. Excellent project management, analytical skills, and interpersonal skills are essential for success in this position. #J-18808-Ljbffr