- Islandwide (Singapore) Singapore

工作地点
职位描述
岗位职责
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
· 10 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.
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