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Automation Engineer (DeltaV, CSV)

External
QUESS SELECTION & SERVICES PTE. LTD. logoQuess Selection & · Singapore
S$66K–S$102K/yrContractUnknownToday
CompliancePerformance Optimization
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Responsibilities

  • Develop and modify Control Modules (CM), Equipment Modules (EM), and Phase-level logic, including CMI/EMI modules.
  • Perform module coding, parameter configuration, and support batch architecture aligned with S88 standards.
  • Support system integration, testing (FAT/SAT), commissioning, and startup activities.
  • Independently author, review, and execute CSV lifecycle documents including URS, FDS, DDS, and IQ/OQ/PQ protocols.
  • Own end-to-end IQ/OQ protocol execution, including deviation handling, discrepancy management, and summary report generation.
  • Ensure compliance with GAMP5, 21 CFR Part 11, and data integrity requirements.
  • Provide troubleshooting support for module logic, batch execution issues, and system performance optimization.
  • Collaborate with cross-functional teams including Manufacturing, QA, CQV, and IT.
  • Required Qualifications & Experience
  • Bachelor's degree in Engineering (Electrical, Instrumentation, Chemical, or related discipline).
  • 4-6+years of experience in DeltaV automation within pharmaceutical/biotech environments.
  • Strong hands-on exposure to CM/EM configuration, phase logic development, and system architecture.
  • Practical experience in coding, parameter handling, and module-level troubleshooting.
  • Proven hands-on experience in CSV protocol drafting and execution (IQ/OQ/PQ), not limited to review or support roles.
  • Good understanding of batch processes and ISA-88 concepts.
  • Rajkumar Renganathan
  • Quess Selection & Services, Singapore
  • EA License Number: 23C2060 Registration ID is R1983662
  • This is in partnership with the Employment and Employability Institute Pte Ltd ("e2i").

Additional Information

Job Description & Requirements Role Overview: DeltaV Engineer with CSV exposure We are seeking a hands-on DeltaV Engineer with CSV exposure to support GMP-regulated pharmaceutical manufacturing projects. The ideal candidate must have deep technical experience at the lower module level(CM/EM/Phase logic) along with involvement in validation lifecycle activities.


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