About this role
As VP, RA you will oversee all facets of the company’s Regulatory Affairs, providing oversight for all US and international regulatory matters, including filings and interactions with regulatory authorities. The VP should be able to think strategically about the development pipeline for the company and assess which products are most likely to move through the regulatory process efficiently. The VP should be able to develop a tight timeline and coordinate the activities of all departments towards achieving a high-quality (defined as first time acceptance) and on-time submission. They should know regulatory road maps for medical devices and preferably combination drug-device products, which will speed up the clinical trial cycle, the regulatory process and garner more government resources.