IT Systems Administrator/Engineer supporting enterprise manufacturing and lab systems in a GMP-regulated (pharma) environment in Singapore. Day to day: system administration, user access management, Tier 2/3 support, vendor coordination, and leading digital rollouts plus the full Computer System Validation lifecycle. Core tech: Windows Server, Microsoft SQL Server, GAMP 5/21 CFR Part 11 compliance
Own end-to-end system administration, user access management, incident troubleshooting, and root cause analysis (RCA) for all supported systems.
Support and have the opportunity to lead digital project execution, including functional testing, user acceptance testing (UAT), and go-live hypercare for new system rollouts and upgrades.
Support and have the opportunity to lead the full Computer System Validation (CSV) lifecycle, including the development and review of URS, FS, RA, IQ/OQ/PQ, test management, and validation summary reports, alongside GMP compliance activities, internal and external audit support, CAPA management, and change control execution.
Coordinate with third-party vendors on system maintenance, issue resolution, and upgrade planning, while providing Tier 2/3 end-user support for all supported tools.
Requirements
Bachelor's degree in Information Technology, Computer Science, Engineering, or a related field.
Minimum 3 years of experience supporting enterprise-grade manufacturing, laboratory, or related operational systems.
Proficient in Windows Server administration, enterprise application management, and user access provisioning/revocation workflows.
Hands-on experience with Microsoft SQL Server, including the ability to write and troubleshoot basic to intermediate SQL queries for data retrieval and issue diagnosis.
Working knowledge of GAMP 5, GMP data integrity requirements, ALCOA+ principles, 21 CFR Part 11, and Annex 11.
Basic understanding of API functionality, system integration patterns, and core networking concepts, including TCP/IP, DNS, and VPN.
Prior experience in GMP, CDMO, or the pharmaceutical industry is strongly preferred.
Direct, hands-on experience in Computer System Validation (CSV) is strongly preferred.
Fluent professional English, both written and verbal.
To apply, please visit and search for Job Reference: 8X5W9RWV
To learn more about this opportunity, please contact Yingying at [email protected]
We regret that only shortlisted candidates will be notified.
GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Lai Yingying | Registration No: R1110239