Gmp Technologies (S) Pte Ltd · MyCareersFuture · 2w
Quality Validation Officer (Computer System Validation-CSV)- 6 Months Contract
Singapore, Central- Posted
- 2026-09-21 (2w)
- Place
- Singapore, Central
- Commitment
- Contract
- Salary
- SGD 4,500 – 6,000 / month
- Experience
- 3+ YOE
- Education
- Diploma
- Department
- Manufacturing
- Source
- MyCareersFuture (the employer’s own listing)
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Skills in this posting
Pharmaceutical IndustryCSV filesExecute validation protocolsSystem ValidationSOLID PrinciplesRisk Assessment
About the role
To provide end-to-end CSV lifecycle support (URS, RA, IQ, OQ, PQ, RTM, VSR) and support implementation and changes for GMP systems including MES, ERP, Lab systems, and automation platforms.
Key responsibilities
• Review and execution of validation protocols and test scripts
• Support implementation and changes for GMP systems including MES, ERP, Lab systems, and automation platforms
• Ensure compliance with GAMP5, 21 CFR Part 11, and Annex 11
• Support change control, deviation, CAPA, and risk assessment activities related to the smart manufacturing project
• Provide documentation support aligned with data integrity (ALCOA+) principles
• Collaborate with QA, IT, Automation, and business stakeholders to ensure project goal is achieved
• Support audit readiness and regulatory inspections specific to topics related to Smart Manufacturing
About you
• Diploma/Degree in Engineering, Life Sciences, IT, Computer Science, Quality, or related discipline with basic understanding of Computer System Validation (CSV) and IT system/software validation
• Familiarity with CSV lifecycle activities including URS, Risk Assessment, IQ, OQ, PQ, RTM, and Validation Summary Reports (VSR)
• Experience supporting validation activities such as protocol execution, test script review, and validation documentation
• Basic knowledge of GMP computerized systems such as MES, ERP, laboratory systems, and automation platforms
• Understanding of GMP regulatory requirements including GAMP5, 21 CFR Part 11, Annex 11, and data integrity principles (ALCOA+)
• Experience supporting quality processes such as change control, deviation, CAPA, and risk assessment activities within a regulated environment
• Good communication and documentation skills with the ability to collaborate with QA, IT, Automation, and business stakeholders in supporting smart manufacturing projects
GMP Technologies (S) Pte Ltd | EA License: 11C3793 | EA Personnel: Dianna| Registration No: R1327268
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Gmp Technologies (S) Pte Ltd
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