Teams at PDDN INC.

Serve as a techno-functional POMS MES SME for pharmaceutical manufacturing. Configure, support, and implement MES solutions while bridging business, quality, validation, and IT teams. Ensure compliant electronic batch records, workflows, GMP/GxP operations, troubleshooting, documentation, and CSV validation. Support regulatory compliance with FDA 21 CFR Part 11 and GAMP 5. Experience with large-scale MES rollouts and ERP, LIMS, or SCADA integrations is advantageous.