Job Description

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 OS
  • Only 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
  • Location: Tuas

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