Job Description

DeltaV Support Engineer

We're seeking a Junior DeltaV support engineer to support pharmaceutical manufacturing operations within a GMP-regulated environment. The engineer will be involved in day-to-day operational support activities for DeltaV systems, troubleshooting manufacturing issues, supporting change controls, and assisting ongoing improvement and project execution activities across the manufacturing environment. This is a long-term engagement with strong exposure to pharmaceutical manufacturing systems, operations, and automation support within a highly regulated life sciences environment.

Key Responsibilities

• Support day-to-day DeltaV operational activities within manufacturing environment
• Perform basic troubleshooting of DeltaV system issues related to manufacturing operations
• Support monitoring and maintenance activities for DeltaV-controlled systems
• Coordinate with Operations, QA, Engineering, and Automation teams for issue resolution
• Support alarm management, batch execution monitoring, and operational investigations
• Assist in system health checks and routine maintenance activities
• Support activities in compliance with cGMP and site quality procedures
• Participate in change control, deviation, and CAPA activities related to automation systems
• Assist in preparation and review of GMP documentation and SOPs
• Support audit readiness and documentation activities
• Support small enhancement and continuous improvement projects within DeltaV environment
• Assist senior engineers during commissioning, testing, and implementation activities
• Participate in FAT/SAT, IQ/OQ support activities where required
• Coordinate with vendors and internal stakeholders during project execution phases
• Support lifecycle management and system upgrade activities
• Manage change control processes related to QC equipment qualification
• Support and lead deviation investigations and resolution activities
  
  

Requirements & Qualifications

• Bachelor's Degree or Diploma in Engineering, Automation, Electrical, Instrumentation, Biotechnology, or related discipline
• 3–5 years of experience in DeltaV support within pharmaceutical, biotech, or life sciences manufacturing environment
• Exposure to Emerson DeltaV systems within GMP-regulated manufacturing operations
• Basic understanding of DeltaV architecture, modules, batch operations, and troubleshooting
• Good understanding of cGMP, GAMP5, and pharmaceutical manufacturing practices
• Exposure to manufacturing operations support and incident handling
• Experience supporting operational manufacturing environment is preferred
• Exposure to commissioning, qualification, or project support activities will be an added advantage