CSV Engineer- Automation-Delta V

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 is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors.

With offices across Europe, Asia and US, our core focus is on consistently delivering high-quality outcomes for our multinational clients.

This focus, and our people's experience in delivering consistent quality results for our clients over the past 20 years has been key to our success to date.

We are currently looking for a CSV Engineer – Pharma to join us on a permanent role to help us deliver various projects in the Life Sciences Industry.

Key Attributes/Responsibilities

• At least 5 years experience in computer systems validation in the pharma industry
• Evaluate test documents and protocols (such as FAT, SAT, and Interface Test) to ensure they meet CSV and QA standards.
• Participate in design meetings at various vendor sites.
• Witness FATs and interface tests at vendor locations.
• Work on the generation and execution of qualification tests, including IQ, OQ, and PQ.
• Provide support for FAT, SAT, IQ, OQ, and PQ processes
• Experience working on Delta V is required

PES International operates as an equal opportunity employer. No terminology in this advert is intended to discriminate on the grounds of age, race, religion, sexual orientation or any other factors with no bearing to employment skills and we confirm that we are happy to accept applications from persons of any background for this role