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Lead CSV activities for laboratory and analytical equipment, ensuring compliance with cGMP, 21 CFR Part 11, and data integrity requirements. Draft and execute validation deliverables (URS, Risk Assessments, Test Scripts, IQ/OQ/PQ, Traceability). Assess and implement audit trail review requirements and system access controls. Bachelor’s degree in Engineering, Computer Science, Life Sciences, or a related field. 5–10 years of hands-on CSV experience with analytical instruments. Strong knowledge of 21 CFR Part 11, audit trails, data integrity, and Windows OS Only open to Singapore Citizens and Permanent Residents. Candidates must have relevant experience in GMP-regulated environments. Tenure: Contract Offered Salary: $5,000 – $5,500 Locat...
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CQV Engineer – Laboratory Systems (CSV Focus)
APBA TG Human Resource Pte Ltd • Singapore, Singapore
About the Role
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