The Automation Engineer 2 will provide support to the Drug Substance Manufacturing (DSM) facility. This includes implementation of changes to the Automation systems, updating design documents, executing testing, troubleshooting events, and being a part of Automation on-call support. During the project phase, the main responsibility as a Computer System Validation (CSV) Automation Engineer 2 will be to prepare validation documentation and contribute to the qualification of Drug Substance Manufacturing (DSM) GxP Automation Computerized Systems. This role will partner with other departments locally and other sites to align strategies and procedures. Once operational, this role will be responsible for ensuring that all DSM GxP Automation Computerized Systems are maintained in a validated state throughout their lifecycle with a focus on consistent policy administration. Additionally, there will be involvement in facilitating improvement initiatives and supporting regulatory agency and third-party inspections.