Global Regulatory Affairs Associate II: Device Submissions

A leading medical device company in San Diego seeks a Regulatory Affairs Specialist to ensure compliance with global submission requirements. Responsibilities include analyzing regulatory requirements, preparing registration packages, and representing global regulatory affairs in team meetings. Candidates should possess a Bachelor's Degree and ideally have two to four years of experience in regulatory affairs. The role offers a competitive salary and a comprehensive benefits package, suited for proactive candidates with strong communication skills. #J-18808-Ljbffr