CSV Engineer: DeltaV GMP Validation Specialist

No deviation Pte Ltd.; Singapore; On-site; SGD 70,000 - 110,000; Full time

Benefits offered by this job

Generous Leave

Health & Wellness

Professional Development

Inclusive Culture

Shape the Future

Job summary

No deviation Pte Ltd. in Singapore seeks a CSV Engineer to validate Emerson DeltaV automation systems in pharma manufacturing.

You will draft and execute test scripts for batch recipes, interlocks, alarms, and sequences, review URS/FS/DS, and support FAT, SAT, IQ, and OQ activities. The role emphasizes GMP/GAMP 5 compliance, strong documentation, and collaboration with Automation, Process Eng, Manufacturing and QA teams.

Qualifications

• Bachelor's degree in related field with CSV experience in pharma.
• Experience drafting and executing validation protocols for automation systems.
• Familiarity with Emerson DeltaV DCS and batch recipes.

Responsibilities

• Develop and execute CSV protocols for Emerson DeltaV automation systems.
• Draft detailed test scripts to validate DeltaV batch recipes, sequences, logic and configurations.
• Review URS, FS and DS to develop validation test cases.
• Verify DeltaV batch recipes, unit procedures, operations, phases and recipe parameters.

Skills

CSV validation

DeltaV knowledge

Documentation

Analytical skills

Cross-functional teamwork

Education

Engineering degree

Chemical Engineering

Tools

DeltaV DCS

Job description

No deviation Pte Ltd. in Singapore seeks a CSV Engineer to validate Emerson DeltaV automation systems in pharma manufacturing.

You will draft and execute test scripts for batch recipes, interlocks, alarms, and sequences, review URS/FS/DS, and support FAT, SAT, IQ, and OQ activities. The role emphasizes GMP/GAMP 5 compliance, strong documentation, and collaboration with Automation, Process Eng, Manufacturing and QA teams.