Vice President of Regulatory Affairs

The organization seeks a Vice President of Regulatory Affairs to lead its global regulatory strategy for Class III medical devices. This executive role involves overseeing regulatory activities to ensure compliance and facilitate timely product development and market access. Key responsibilities include developing regulatory strategies, managing FDA submissions, and collaborating with cross-functional teams to integrate regulatory considerations throughout the product lifecycle. The ideal candidate will possess extensive experience in regulatory pathways for medical devices, strong leadership skills, and the ability to navigate complex regulatory environments. A background in clinical evidence requirements and global market regulations is…