DeltaV Support Engineer

Advanced Manufacturing Tech Solutions (AMTSOL); Singapore; On-site; SGD 42,000 - 68,000; Full time

Job summary

Advanced Manufacturing Tech Solutions (AMTSOL) seeks a Junior DeltaV support engineer to assist pharmaceutical manufacturing operations within a GMP-regulated environment. The role focuses on day-to-day DeltaV operational support, troubleshooting, and assisting with change controls and ongoing improvement across the manufacturing environment.

You will collaborate with Operations, QA, Engineering, and Automation teams to resolve issues, perform system health checks, support alarm management and

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.

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.

Skills

DeltaV troubleshooting

Manufacturing operations support

GMP compliance

Education

Bachelor's degree or Diploma in Engineering/Automation

Tools

Emerson DeltaV

Job description

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