Location
D01 Cecil, Marina, People’s Park, Raffles Place
Job Type
Full-time
Experience
Mid
Category
General
Salary
$4,000 - $8,000
Posted
2 days ago
Expires
Feb 11, 2026
Views
1

Job Details

Vacancies

1 position

Experience Required

No experience required

Job Description

Job Description

  • Contribute to Life Science projects for Antaes Asia clients
  • Develop and execute CQV documentation including commissioning protocols, FAT/SAT reports, IQ/OQ/PQ protocols, summary reports, and traceability matrices.
  • Support end-to-end CQV lifecycle for process, utility, and support systems — e.g. bioreactors, chromatography skids, filtration units, CIP/SIP, WFI, HVAC, autoclaves, and clean utilities.
  • Participate in design reviews (URS, FDS, P&ID walkdowns) to ensure CQV considerations are integrated during project design and construction.
  • Manage execution of commissioning and qualification activities in alignment with project schedules, safety standards, and GMP compliance.
  • Support automation qualification (DeltaV, PLC, SCADA) and ensure integration with process control systems.
  • Review vendor documentation and coordinate FAT and SAT with suppliers and engineering teams.
  • Troubleshoot and resolve technical issues encountered during CQV execution.
  • Ensure all CQV deliverables meet internal Quality and Validation standards and align with site Validation Master Plan (VMP).
  • Support handover of qualified systems to Manufacturing and Maintenance teams, including training and documentation.
  • Collaborate closely with cross-functional teams including Engineering, QA Validation, Manufacturing, and Automation.
  • Contribute to the promotion of Antaes services on top of assistance provided to clients

Job Requirements

  • Bachelor’s Degree in Chemical, Mechanical, Biomedical, or related Engineering field.
  • 3–7 years of CQV experience in the pharmaceutical industry
  • Strong understanding of GMP, GEP, ISPE Baseline Guides, ASTM E2500, and FDA/EMA validation expectations.
  • Experience in process equipment qualification (bioreactors, chromatography, UF/DF, CIP/SIP), clean utilities, and automation integration.
  • Familiar with risk-based CQV approach and change control processes.
  • Proficiency with documentation management systems (e.g., Veeva)
  • Candidate must be highly motivated, be able to work independently as well as in a team and have good organizational and oral and written communication skills
  • Excellent communication skills, both written and verbal, in English - to communicate and work with English speaking counterparts

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ANTAES ASIA PTE. LTD.

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