DeltaV Support Engineer (Automation)

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.

Key Responsibilities

. Support day-to-day DeltaV operational activities within the 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 the preparation and review of GMP documentation and SOPs
. Support audit readiness and documentation activities
. Support small enhancement and continuous improvement projects within the 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 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 a 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, pharmaceutical manufacturing practices
. Exposure to manufacturing operations support and incident handling
. Experience supporting an operational manufacturing environment is preferred
. Exposure to commissioning, qualification, and project support activities will be an added advantage.