CSV Engineer: GMP DeltaV Validation Specialist
NO DEVIATION PTE. LTD.
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Benefits offered by this job
Job summary
NO DEVIATION PTE. LTD. seeks a CSV Engineer to validate Emerson DeltaV automation systems in a pharmaceutical environment.
You will draft and execute protocols, ensure GMP/GAMP5 compliance, and collaborate with Automation, Process Engineering, Manufacturing, and Quality Assurance teams. Prior DeltaV experience and Part 11 knowledge are advantageous. The role involves FAT/SAT/IQ/OQ support, discrepancy investigations, and maintaining requirements traceability to validation reports.
Qualifications
- Bachelor’s degree in Engineering or related discipline with CFA/CSV exposure.
- Experience drafting/ executing validation protocols for automation systems in pharmaceutical/biopharma.
- Familiarity with DeltaV DCS, batch recipes and control modules is preferred.
Responsibilities
- Develop and execute CSV protocols for Emerson DeltaV automation systems.
- Draft test scripts to validate batch recipes, sequences, and control logic.
- Review URS/FS/DS to produce validation test cases; verify DeltaV batch recipes and parameters.
- Support FAT, SAT, IQ, OQ activities and document results.
- Maintain traceability between specs, protocols, and test results.
Skills
Education
Tools
Job description
NO DEVIATION PTE. LTD. seeks a CSV Engineer to validate Emerson DeltaV automation systems in a pharmaceutical environment.
You will draft and execute protocols, ensure GMP/GAMP5 compliance, and collaborate with Automation, Process Engineering, Manufacturing, and Quality Assurance teams. Prior DeltaV experience and Part 11 knowledge are advantageous. The role involves FAT/SAT/IQ/OQ support, discrepancy investigations, and maintaining requirements traceability to validation reports.
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