The Sr. Process Validation Engineer is responsible for leading the development, implementation, and validation of complex manufacturing processes supporting the Company’s cell therapy programs.
This role operates with a high degree of autonomy and technical judgment, serving as a subject matter expert for fill/finish, container closure systems, and process validation activities across late-stage development and commercial readiness. The position partners cross-functionally with MSAT, Manufacturing, Facilities, Device, R&D, Regulatory, and Bioinformatics to enable robust, compliant, and scalable GMP manufacturing processes and to support regulatory submissions.