Were 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
Bachelors Degree or Diploma in Engineering Automation Electrical Instrumentation Biotechnology or related discipline
35 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
DeltaV Support Engineer Overview Were 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 sup...
DeltaV Support Engineer
Overview
Were 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
Bachelors Degree or Diploma in Engineering Automation Electrical Instrumentation Biotechnology or related discipline
35 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