JOB SUMMARY: The Mid-Level FDA Regulatory Associate will be part of the Legal team, and will support the VP, Lead Regulatory Counsel, who is broadly responsible for providing the business with strategic advice and counsel on regulatory issues. The Associate will also support the Global Regulatory Affairs function with US FDA regulatory expertise in support of obtaining and maintaining clinical and commercial regulatory approvals in alignment with business objectives.  The Associate will work closely with the Global Regulatory Affairs function, providing guidance and expertise in support of US regulatory product submissions.  In addition, the Associate will play an important role in developing regulatory infrastructure and documentation templates