GMP IT Systems Engineer – Digital Innovation & CSV

GMP Technologies; Singapore; Sur place; SGD 70 000 - 110 000; Plein temps

Résumé du poste

GMP Technologies is seeking an IT Systems Administrator / Engineer (Digital Innovation) in Singapore to own end-to-end system administration, user access management, incident troubleshooting, and RCA for all supported systems. The role includes leading digital projects, functional testing, UAT, and go-live hypercare for new rollouts and upgrades.

You will also drive the CSV lifecycle, develop and review URS/FS/RA/IQ/OQ/PQ, ensure GMP data integrity, support audits, CAPA, and change control while

Qualifications

• Bachelor's degree in IT, CS, engineering or related field.
• Minimum 3 years in enterprise-grade manufacturing or lab systems.
• Fluent professional English; strong GMP/CSV experience preferred.

Responsabilités

• Own end-to-end system administration, user access management, incident troubleshooting, and RCA for all supported systems.
• Support and have the opportunity to lead digital project execution, including functional testing, UAT, and go-live hypercare.
• Lead the full Computer System Validation (CSV) lifecycle, including URS, FS, RA, IQ/OQ/PQ, test management, and validation reports, with GMP audit support and CAPA management.

Connaissances

System administration

Incident troubleshooting

Root cause analysis

UAT oversight

CSV management

GMP compliance

Vendor coordination

End-user support

SQL queries

Windows Server

Formation

Bachelor's degree in IT/CS/Engineering

Outils

SQL Server

Windows Server

Description du poste

GMP Technologies is seeking an IT Systems Administrator / Engineer (Digital Innovation) in Singapore to own end-to-end system administration, user access management, incident troubleshooting, and RCA for all supported systems. The role includes leading digital projects, functional testing, UAT, and go-live hypercare for new rollouts and upgrades.

You will also drive the CSV lifecycle, develop and review URS/FS/RA/IQ/OQ/PQ, ensure GMP data integrity, support audits, CAPA, and change control while