
The Director of Engineering, Facilities, and Validation leads the strategic and operational management of a GMP commercial vaccine manufacturing site in Canton, MA. This role oversees engineering, facilities, utilities, maintenance, and validation functions to ensure reliable, compliant, and inspection-ready operations. Key responsibilities include managing capital expenditure planning and execution, leading qualification and validation programs, and directing site shutdowns and major maintenance windows. The position requires partnering with cross-functional teams to drive continuous improvement and maintain regulatory compliance with FDA and EMA standards. This opportunity appeals to leaders seeking to contribute to a mission-driven public health company dedicated to saving lives. The role offers the chance to build and develop a high-performing organization within a collaborative culture that values safety and quality.


















