Computer System Validation Engineer (PLC/ SCADA/ Pharma)

Location Singapore
Discipline Engineering
Job Reference BBBH137950_1714632594
Salary S$4000 - S$5000 per month
Consultant Email
EA License No. 02C3423

Computer System Validation (PLC/ SCADA/ Pharma)

Duration: 12 months (Renewable)
Location: Tuas
Salary : Up to $5000 depending on experience
Industry : Pharmaceutical


  • Understand development of Computer System Validation (CSV) and equipment specifications and executing Computer System Validation, System Development Life Cycle (SDLC), and other pharmaceutical equipment/system commissioning/validation such as installation qualification (IQ), operational qualification (OQ), performance qualification (PQ) protocols in accordance with Good Engineering Practices, GAMP, local SOPs, industry best practices and other industry related guidance documents.
  • Assess the impact of changes to cGMP equipment/systems and methods and establish the applicable Validation Plan to ensure the validated status following changes.
  • Experience in technical writing and report generation of testing methodologies of automated systems.
  • Expertise in evaluating validation protocols and summary reports.
  • Adept understanding of Testing and Software Development Lifecycle and QA methodologies.
  • Responsible for being a quality contact and primary Subject Matter Expert (SME) for complex deviations for systems, processes, and equipment related to engineering, facilities, automation, manufacturing, and validation.
  • Support and review complex deviation investigations related to manufacturing process equipment, utilities, automation, validation, and engineering.
  • Work closely with Operations, Facilities, Manufacturing, Automation, Validation, and Engineering to resolve open issues resulting from equipment failures, issues, and deviation record reviews.
  • Lead the QA review and assessments of deviations; includes performing risk assessments, leading root cause analysis investigations, tracking, follow-up, close out, and reporting/trending.


  • At least 2 years of demonstrated experience in cGMP automation/computerized systems, quality, and compliance areas in the pharmaceutical industry.
  • Thorough understanding of industry standards and best practices for computer system validation.
  • Extensive experience with validation of equipment controlled by PLCs, BAS/BMS systems, and other typical automated system platforms

Lim Pey Chyi (Apple) -
Recruitment Consultant (R2090579)
Manpower Staffing Services (S) Pte Ltd
EA Licence: 02C3423

Apple, Pey Chyi Lim EA License No.: 02C3423 Personnel Registration No.: R2090579

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