
CURIA is a CDMO partnering with customers to make treatments accessible through its biologics and small molecule expertise.
Curia is seeking a Senior Principal Validation Engineer to oversee Validation Contractors for the Albuquerque expansion. This role involves supervising validation activities, managing projects, and ensuring compliance with GMP regulations. The engineer will also contribute to new product introductions, equipment re-qualification, and system installation. The position requires expertise in pharmaceutical validation, project management, and strong communication skills.