DeltaV Automation Engineer: Validation, CQV & SAT Lead

CUTE SOLUTIONS & SERVICES PTE. LTD.; Singapore; On-site; SGD 100,000 - 140,000; Full time

Job summary

CUTE SOLUTIONS & SERVICES PTE. LTD. seeks an experienced automation engineer to lead DeltaV DCS projects and validation efforts in regulated environments.

You will configure DeltaV components, author IQ/OQ/IOQ protocols, and ensure clean, compliant system administration across development, test and production settings. You will coordinate CQV activities with cross-functional teams, support upgrades, and deliver robust validation documentation in line with GMP, FDA, EU Annex 11, and other

Qualifications

• 5+ years in automation engineering with DeltaV DCS.
• Experience with validation/compliance in GMP/FDA/EU Annex 11.
• Experience with IQ, OQ, PQ, IOQ protocols.
• Knowledge of MES, OPC DA/UA, Fieldbus, and HMI systems.
• Strong SDLC and change control documentation.
• Excellent analytical, troubleshooting, and documentation skills.
• Ability to lead cross-functional teams and train junior engineers.

Responsibilities

• Configure DeltaV Batch: recipes, phases, EM, CM.
• Lead DeltaV system validation: IQ/OQ/IOQ.
• Maintain configuration integrity across dev/test/prod environments.
• Troubleshoot and support DeltaV DCS integration.
• Lead automation commissioning and SAT for upgrades.
• Coordinate CQV activities with cross-functional teams.
• Prepare validation docs for DeltaV and Rockwell BAS per regulations.
• Liaise with vendors, IT, and stakeholders for upgrades.
• Provide routine ops support during maintenance and shutdowns.
• Perform incident resolution and root-cause analysis.

Skills

Project management

Stakeholder communication

Analytical skills

Troubleshooting

Documentation

Tools

DeltaV DCS

Rockwell BAS

SCADA

Allen-Bradley PLC

Yokogawa PLC

Invensys PLC

Job description

CUTE SOLUTIONS & SERVICES PTE. LTD. seeks an experienced automation engineer to lead DeltaV DCS projects and validation efforts in regulated environments.

You will configure DeltaV components, author IQ/OQ/IOQ protocols, and ensure clean, compliant system administration across development, test and production settings. You will coordinate CQV activities with cross-functional teams, support upgrades, and deliver robust validation documentation in line with GMP, FDA, EU Annex 11, and other