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The MBR Author will be responsible for PAS-X MES design, development, and documentation within biopharmaceutical environments. Duties include gathering user requirements, configuring electronic batch records, developing qualification documentation, and supporting the implementation of system updates. The role requires experience in the SDLC of automated computer systems especially in the context of life sciences.

The MES Engineer will design and maintain MES solutions using Siemens OpsCenter in life sciences manufacturing. This role requires collaboration with teams to fulfill project specifications, troubleshooting MES systems, executing validation protocols, and documenting compliance activities. The engineer will also train other team members on MES best practices.

The Quality Engineer will develop and implement quality control and assurance strategies for cell and gene therapy products, perform risk assessments, review technical documents, conduct audits, and ensure compliance with regulatory requirements. They will also troubleshoot quality issues and collaborate with cross-functional teams on quality improvement initiatives.