Director Regulatory Affairs

The Director Regulatory Affairs serves as a key member of the global regulatory team, acting as a strategic business partner to develop and implement robust US regulatory strategies for assigned projects. This role involves leading interactions with the FDA, overseeing the preparation of critical submission documents, and providing guidance across the entire product life cycle from pre-approval to post-approval activities. The position requires close collaboration with cross-functional teams to ensure successful product launches, commercialization, and compliance with regulatory requirements.