Global CMC Regulatory Director - Gene Therapy

A global life sciences company in North Carolina is seeking a Regulatory Affairs professional to lead CMC regulatory strategy and activities. The role involves collaboration with various stakeholders to ensure compliance with global regulatory requirements for drug submissions. Candidates should have at least 10 years of industry experience, including 6 years in regulatory affairs, and a BS in Chemistry or related field. This position offers a competitive salary, hybrid working solutions, and opportunities for professional growth. #J-18808-Ljbffr