Posted:
February 21, 2026
Location:
Tuas, Tuas, Singapore

Job Description

Job Description & Requirements

  • Lead QA oversight for computer system validation (CSV) activities ensuring compliance with cGMP, GAMP 5, 21 CFR Part 11, and Annex 11 standards
  • Review user requirement specifications (URS) and risk assessments to ensure thorough validation planning and risk mitigation
  • Oversee installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ) activities to verify system functionality and compliance
  • Ensure data integrity by applying ALCOA+ principles and managing change controls throughout validation and implementation processes
  • Act as the QA representative for system upgrades and new system implementations, collaborating closely with IT, Validation, and Engineering teams to drive project success
  • Apply strong CSV and QA project management skills to deliver compliant and efficient validation outcomes within a GMP environment, preferably in pharmaceutical or biologics...

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Job Overview

Job Type: Full-time
Location: Tuas, Singapore
Posted: February 21, 2026
Deadline: April 02, 2026