The Principal Specialist, QA Compliance ensures adherence to Moderna's Quality Management System in a pharmaceutical setting. Responsibilities include maintaining compliance, overseeing records management, supporting audits and inspections, and driving continuous improvement initiatives. The role requires strong collaboration across teams to foster a culture of quality and operational excellence.

As the Manager of Site Planning, you will enhance planning processes in Moderna's Supply Chain Planning team, ensuring efficient delivery of innovative mRNA products. Focused on production planning and collaboration across teams, you'll track performance metrics and contribute to continuous improvement initiatives.

The role involves leading digital innovation in a GMP manufacturing environment at Moderna's Clayton site by managing IT operations, digital strategy execution, and team development, ensuring compliance with manufacturing regulations, and promoting technological advancements.

The Sr. Specialist in Supply Chain Compliance is responsible for managing compliance documentation, reviewing and optimizing SOPs, training local teams, ensuring regulatory adherence, and collaborating with cross-functional teams. This role focuses on maintaining GMP standards and improving supply chain processes within a highly regulated environment.

The Principal Specialist in QA Technical Operations at Moderna will oversee compliance and quality management for materials within a GMP-regulated environment, ensuring efficient operations, troubleshooting, and system optimization, and leading quality oversight in manufacturing and warehouse processes.