Manager, MES

Role: Lead the MES (Manufacturing Execution System) team for pharmaceutical site operations, focusing on developing, validating, and troubleshooting POMS recipes to ensure compliance with global IT standards and seamless integration with systems like Maximo, SAP, and Automation. Responsibilities: manage recipe authoring, design POMS for site processes, oversee validation and re-validation strategies, lead FMEA activities, develop SOPs, and drive continuous improvement projects. Act as a liaison with stakeholders, support data integrity, and ensure EHS compliance. Qualifications: Bachelor's in Business, Engineering, or Computer Science; 8+ years in pharma manufacturing or quality, with 3+ years hands-on MES experience; strong validation skills, project management, and communication. Preferred: Master's degree, GMP knowledge, leadership skills, and experience with system integrations. HighValue: pharma manufacturing, MES systems, recipe development, validation, GMP compliance, cross-system integration (SAP, Maximo), and process optimization. WorkSetup: not specified; likely on-site or hybrid based on typical manufacturing site operations.