
The Associate Director, Quality role at Kiniksa Pharmaceuticals provides leadership for GMP technical transfer activities within the commercial manufacturing division. Key responsibilities include overseeing process transfers from development to commercial sites, approving validation strategies, and ensuring compliance with global regulatory standards for both drug substance and product. The position requires managing external partners, leading quality risk assessments, and serving as the primary point of contact for regulatory inspections. This opportunity appeals to professionals seeking to drive innovation in cardiovascular therapies within a collaborative, patient-first culture. The role is based onsite in Lexington, Massachusetts, with occasional travel required.













