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Support, maintain, and improve GMP-critical manufacturing IT systems (MES, LIMS, historians, EBRs), ensure IT/OT integration and compliance with GxP/data-integrity, troubleshoot and perform root-cause analysis, participate in validation (IQ/OQ/PQ), manage networking and cybersecurity controls, and collaborate with cross-functional teams to implement analytics and ensure alignment with corporate IT and disaster recovery requirements.

The role involves executing engineering activities, performing validation tasks, technical writing, and ensuring compliance with GMP regulations.

Lead engineering activities for facilities and equipment in a GMP-compliant environment. Oversee projects, manage qualifications, and ensure regulatory compliance.

Lead and manage multiple validation and qualification projects in a GMP-compliant environment, ensuring compliance with regulatory standards and operational efficiency.