Client Name: Oxford Global Resources
End Client Name: Pharmaceutical/Biotech manufacturing domain
Job Title: Sr. Automation Engineer
Location: Ohio New Jersey RTP NC Upstate NY Boston MA
Work Type: Onsite (Hybrid is an option but more onsite is better)
Job Type: Contract
Rate: $80/hr on W2 (depending on tenure)
LinkedIn needed sample resume added above
Notes:
- Candidates must be local; no relocation assistance.
- US Citizens / Green Card only.
- Start Date: ASAP
- Must have pharmaceutical/biotech manufacturing experience
- Good experience with DeltaV Allen-Bradley PLCs and SCADA/HMI systems
- LOA (Length of Assignment) is expected to be long-term
Job Description:
Seeking an experienced Automation Engineer to support troubleshoot and optimize automated processes in a regulated GMP environment.
Roles and Responsibilities:
- Design configure and maintain DeltaV Batch systems (Control Modules Equipment Modules Unit Procedures Phases) following ISA-88 standards.
- Develop and modify Allen-Bradley ControlLogix PLC logic to optimize equipment sequencing and performance.
- Program configure and troubleshoot SCADA/HMI systems (FactoryTalk View SE/ME).
- Support commissioning and start-up of automated equipment including I/O checks logic verification and FAT/SAT testing.
- Troubleshoot automation issues in sensors actuators VFDs control networks and industrial hardware.
- Ensure system compliance with GMP GAMP5 and 21 CFR Part 11 regulations.
- Integrate DeltaV and PLC systems with data historians (OSI PI FactoryTalk Historian) for monitoring and reporting.
- Collaborate with cross-functional teams (Manufacturing QA IT Validation Maintenance) to resolve production-impacting automation issues.
- Author and execute technical documentation including URS FRS DDS IQ/OQ/PQ protocols change controls and CAPA support.
- Provide day-to-day support for production lines and utilities (HVAC WFI Clean Steam EMS/BMS).
Required Skills:
- 6 years in automation engineering within pharmaceutical/biotech manufacturing
- Good expertise with DeltaV Batch configuration and recipe management
- Strong background in Allen-Bradley ControlLogix PLC programming and troubleshooting
- Experience with FactoryTalk View SE/ME OSI PI FactoryTalk Historian
- Knowledge of GMP FDA compliance and regulated manufacturing environments
- Ability to read and update I/O lists wiring diagrams loop diagrams and control narratives
- Experience supporting commissioning validation and audit readiness
- Experience with Siemens BAS/EMS systems
- Knowledge of serialization systems AVI systems and packaging automation
- Exposure to network troubleshooting (Ethernet/IP ControlNet)
- Bachelors degree in Electrical Electronics Automation or related Engineering field
For recruiters-
Automation Engineer Pharma Automation DeltaV Emerson DeltaV Batch Allen-Bradley ControlLogix PLC Programmer HMI SCADA FactoryTalk View GMP GAMP5 OSI PI Historian Validation Pharma Manufacturing
Client Name: Oxford Global Resources End Client Name: Pharmaceutical/Biotech manufacturing domain Job Title: Sr. Automation Engineer Location: Ohio New Jersey RTP NC Upstate NY Boston MA Work Type: Onsite (Hybrid is an option but more onsite is better) Job Type: Contract Rate: $80/hr on W2 (dependi...
Client Name: Oxford Global Resources
End Client Name: Pharmaceutical/Biotech manufacturing domain
Job Title: Sr. Automation Engineer
Location: Ohio New Jersey RTP NC Upstate NY Boston MA
Work Type: Onsite (Hybrid is an option but more onsite is better)
Job Type: Contract
Rate: $80/hr on W2 (depending on tenure)
LinkedIn needed sample resume added above
Notes:
- Candidates must be local; no relocation assistance.
- US Citizens / Green Card only.
- Start Date: ASAP
- Must have pharmaceutical/biotech manufacturing experience
- Good experience with DeltaV Allen-Bradley PLCs and SCADA/HMI systems
- LOA (Length of Assignment) is expected to be long-term
Job Description:
Seeking an experienced Automation Engineer to support troubleshoot and optimize automated processes in a regulated GMP environment.
Roles and Responsibilities:
- Design configure and maintain DeltaV Batch systems (Control Modules Equipment Modules Unit Procedures Phases) following ISA-88 standards.
- Develop and modify Allen-Bradley ControlLogix PLC logic to optimize equipment sequencing and performance.
- Program configure and troubleshoot SCADA/HMI systems (FactoryTalk View SE/ME).
- Support commissioning and start-up of automated equipment including I/O checks logic verification and FAT/SAT testing.
- Troubleshoot automation issues in sensors actuators VFDs control networks and industrial hardware.
- Ensure system compliance with GMP GAMP5 and 21 CFR Part 11 regulations.
- Integrate DeltaV and PLC systems with data historians (OSI PI FactoryTalk Historian) for monitoring and reporting.
- Collaborate with cross-functional teams (Manufacturing QA IT Validation Maintenance) to resolve production-impacting automation issues.
- Author and execute technical documentation including URS FRS DDS IQ/OQ/PQ protocols change controls and CAPA support.
- Provide day-to-day support for production lines and utilities (HVAC WFI Clean Steam EMS/BMS).
Required Skills:
- 6 years in automation engineering within pharmaceutical/biotech manufacturing
- Good expertise with DeltaV Batch configuration and recipe management
- Strong background in Allen-Bradley ControlLogix PLC programming and troubleshooting
- Experience with FactoryTalk View SE/ME OSI PI FactoryTalk Historian
- Knowledge of GMP FDA compliance and regulated manufacturing environments
- Ability to read and update I/O lists wiring diagrams loop diagrams and control narratives
- Experience supporting commissioning validation and audit readiness
- Experience with Siemens BAS/EMS systems
- Knowledge of serialization systems AVI systems and packaging automation
- Exposure to network troubleshooting (Ethernet/IP ControlNet)
- Bachelors degree in Electrical Electronics Automation or related Engineering field
For recruiters-
Automation Engineer Pharma Automation DeltaV Emerson DeltaV Batch Allen-Bradley ControlLogix PLC Programmer HMI SCADA FactoryTalk View GMP GAMP5 OSI PI Historian Validation Pharma Manufacturing
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