We are seeking an experienced Automation Engineer to support the implementation and integration of DeltaV MES for drug substance manufacturing. This position involves configuring systems for paperless manufacturing with ERP/MES/DCS integration, troubleshooting, and collaborating with cross-functional teams to ensure smooth project execution.

Key Responsibilities:

• Support the design and implementation of an Emerson Syncade (DeltaV MES) Manufacturing Execution System.
• Participate in project status meetings and provide input on system requirements and lifecycle documentation.
• Configure MES functions, including: 
  • Order Management
  • Material Management
  • Workflow Execution
  • Electronic Batch Record (EBR)
  • Quality Review Manager (QRM)
  • Weigh & Dispense
• Coordinate with Automation, CSV, CQV, Utilities, Process Engineering, QA, and other project teams.
• Perform simulation of DeltaV MES logic and resolve issues.
• Assist with configuration migration between sites and internal systems.
• Develop and maintain Configuration Management processes to ensure data integrity.
• Complete safety and project-specific training as required.

Experience & Skills:

• 5+ years of experience designing, configuring, and implementing Manufacturing Execution Systems.
• 3+ years of experience with Emerson Syncade (DeltaV MES).
• Proficiency in debugging MES configuration.
• Familiarity with cGMP standards, FDA regulations, S88 batch models, ISA 95, GAMP5, and 21 CFR Part 11.
• Knowledge of VB Script, XML/XPATH/XSLT, and SQL/TSQL is a plus.
• Experience with Emerson DeltaV, OSIsoft PI, and InfoBatch is advantageous.
• Strong written and verbal communication skills.

Additional Details:

• Expected to work 40 hours per week.
• Onsite requirement: 4 days per week; 1 day remote.
• Initial project duration: 6 months with potential extensions for future projects.