United States$170K - $210K per year10+ yrs expOthers
The Associate Director will oversee the entire drug product development lifecycle, including pre-formulation, manufacturing, and technology transfer. They will act as the primary point of contact for CDMOs and ensure all processes comply with regulatory standards and quality requirements.
United Kingdom, United States$235K - $270K per year10+ yrs expLegal
The Director/Senior Director, Regulatory CMC is responsible for developing and executing global regulatory strategies for CMC activities across the company's clinical product portfolio. This role involves leading interactions with regulatory agencies and providing guidance on CMC matters to cross-functional teams to ensure compliance and timely approvals.
