The Director provides enterprise Quality and Regulatory governance for U.S. operations, ensuring compliance with 21 CFR Parts 210 and 211. They lead the Quality Management System, oversee inspection readiness, and manage cross-functional quality initiatives across manufacturing facilities.
The Program Manager will lead the development and implementation of AI, automation, and digital transformation roadmaps for Quality & Regulatory operations. They are responsible for designing and deploying technology solutions that improve compliance, data visibility, and operational efficiency across the organization.
The Project Manager will oversee the design, construction, and commissioning of radiopharmacy facilities and new business initiatives. They are responsible for managing project budgets, schedules, vendor relationships, and ensuring compliance with FDA, USP, and CFR regulations.
