Quality & Regulatory Director, ISO 13485 - Hands-On Leader

A boutique medical device partner is seeking a Quality & Regulatory Affairs Director to oversee quality operations, ensuring compliance with ISO 13485 standards. The role involves managing a small quality team while implementing CAPA and continuous improvement initiatives, providing an opportunity to significantly influence quality processes in a collaborative environment. Candidates should have a strong background in quality leadership within the medical device field and be ready to engage hands-on with team members. This position offers high visibility and impactful work with executive leadership in Miami. #J-18808-Ljbffr