Job Responsibilities:
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.Job Requirements:
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 OSOnly open to Singapore Citizens and Permanent Residents.Candidates must have relevant experience in GMP-regulated environments.Please send a copy of your resume to [email protected]
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Tenure: Contract Offered Salary: $5,000 – $5,500 Locat...