
The Quality Assurance Specialist I role at Curia supports a global contract development and manufacturing organization dedicated to advancing life-saving pharmaceutical therapies. Based in Springfield, MO, the position requires a Bachelor's degree in a life science field and focuses on maintaining product quality and patient safety within cGMP production environments. Key responsibilities include monitoring manufacturing activities for regulatory compliance, reviewing batch records and documentation for accuracy, and managing deviation investigations alongside cross-functional teams. The role appeals to candidates seeking a mission-driven career where quality and integrity are central to daily operations. It offers immediate access to comprehensive benefits, paid training, and significant opportunities for professional growth and education reimbursement within a collaborative culture.



















