Purpose of the Role:
The DeltaV Platform Engineer for this project will work closely with the automation team to support the DeltaV Systems (Production, Test & Development Systems).
You will need:
2 years working in GMP environment Pharma or Biotech engineering, operations, or manufacturing
Preferable, 4 years supporting DeltaV platforms/applications including virtual infrastructure, patching, hardware (including PK Controllers, Charms etc.) etc.
Experience in troubleshooting during instrument commissioning for both charm and profibus I/O
Demonstrated teamwork abilities
Knowledge of GMP's, regulatory requirements and computer system validation
Good written and verbal communication skills for both technical and non-technical audiences.
Primary point of contact for DeltaV platform administration.
Front line support and troubleshooting of the DeltaV Platform.
Manage user access to the DeltaV systems following project processes.
Plan and co-ordinate scheduled system maintenance activities for the DeltaV systems e.g. reviewing KBA's, implementing software updates and patches, PM activities etc. following project processes.
Accountable for data management for the DeltaV systems e.g. Backup and Recovery etc
Support the creation of site SOPs for DeltaV platform administration, in addition to supporting generation of BCPs and DRPs.
Support data integrity assessments on the DeltaV platform.
Support setup of the DeltaV OPC UA servers (to communicate with synTQ) and the DeltaV OPC DA servers (to communicate with Syncade).
Support setup of DeltaV applications to communicate with Syncade (event monitor, campaign manager etc.)
Respond to out of hours issues for system administration support if required.
Support troubleshooting of DeltaV hardware during project instrument loop checks for Charm and profibus I/O
Change out charm/terminal blocks in charm panels if required as per modifications to I/O index.
Staffing and RecruitingPharmaceuticalsElectrical/Electronic Manufacturing