Pharma CSV Engineer (DeltaV) – Validation & Automation

EFOR (formerly Process Engineering Specialists); Singapore; On-site; SGD 90,000 - 130,000; Full time

Job summary

PES International is seeking a CSV Engineer – Pharma to join our life sciences projects in Singapore. You will leverage 5+ years in computer systems validation within the pharmaceutical industry to help ensure CSVQA compliance across multiple validation stages.

Responsibilities include evaluating test documents, witnessing FATs and interface tests, and contributing to IQ/OQ/PQ qualification activities, with hands-on DeltaV experience across vendor sites.

Qualifications

• 5+ years in computer systems validation in the pharma industry.
• Experience evaluating test documents and protocols for CSV/QA standards.
• Familiarity with IQ/OQ/PQ qualification activities.

Responsibilities

• Evaluate test documents and protocols (FAT, SAT, Interface Test) to meet CSV/QA standards.
• Participate in design meetings at vendor sites.
• Witness FATs and interface tests at vendor locations.
• Generate and execute qualification tests, including IQ, OQ, and PQ.
• Provide support for FAT, SAT, IQ, OQ, and PQ processes.
• Experience working on Delta V is required.

Skills

CSV in Pharma

Regulatory compliance

Tools

DeltaV

Job description

PES International is seeking a CSV Engineer – Pharma to join our life sciences projects in Singapore. You will leverage 5+ years in computer systems validation within the pharmaceutical industry to help ensure CSVQA compliance across multiple validation stages.

Responsibilities include evaluating test documents, witnessing FATs and interface tests, and contributing to IQ/OQ/PQ qualification activities, with hands-on DeltaV experience across vendor sites.