Manufacturing Automation Specialist
Core
Independently manages digital record lifecycle activities and provides front-line support for Manufacturing Execution System (MES) execution.
Role type
Manufacturing Automation Specialist (MES Digital Record Author)
Builds
MES digital records and system integrity
Domain
Pharmaceutical manufacturing / Process Automation
Deliverable
production ML models | product features | dashboards & analysis | client delivery | infrastructure | physical/clinical work
Required skills
MES digital records management, Deviation investigations, Root cause analysis, Corrective action management, Data integrity management, Cross-functional collaboration, Issue management, Preventive action, Process manufacturing knowledge
Preferred skills
cGMP regulations, Process Automation System Life Cycle methodologies, SAP Architecture, SAP Best Practices, SAP Business ByDesign, SAP Business Planning and Consolidation, SAP Business Warehouse, SAP Consulting, SAP CRM, SAP Development, SAP Implementations, SAP Knowledge, SAP Logistics, SAP Procurement, SAP Project Management, SAP Service Management, SAP Systems, Technical Quality Assurance, Troubleshooting, Automation Engineering, Lean Management, Quality Control Systems
Responsibilities
Author, update, and maintain MES digital records; Ensure compliance with MES standards and data integrity; Provide Level 1 troubleshooting support for MES-related issues; Participate in deviation investigations and root cause analysis; Collaborate with cross-functional teams to align records with manufacturing processes; Support onboarding and knowledge sharing with less experienced authors
Seniority
Mid-level, hands-on IC
