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The Compliance Coordinator is responsible for overseeing validation deviations, CAPAs, change controls, and supporting validation activities in a pharmaceutical environment. This role involves coordinating audits, managing equipment maintenance, and ensuring compliance with inspection standards.

The role involves supporting clients by providing technical expertise in automation systems, troubleshooting, implementing change control procedures, managing event reports, and leading continuous improvement initiatives in the life sciences sector.

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.