Validation Engineers – Temperature Mapping

Validation Engineers – Temperature Mapping & Laboratory Systems (CSV)

Location: Tuas, Singapore

Type: Contract

We are looking for
Validation Engineers
to join a leading project in Tuas, with opportunities in two specialized areas:

Validation Engineer – Temperature Mapping

What you'll do

• Plan and execute
  temperature mapping studies
  for chambers (refrigerators, freezers, incubators, warehouses, etc.).
  
  
• Prepare and execute
  validation protocols, reports, and data integrity assessments
  .
  
  
• Perform
  IQ/OQ/PQ qualification
  in line with GDP and ALCOA principles.
  
  
• Support audits and inspections by providing validation evidence.
  
  
• Review SOPs, deviations, and CAPAs related to temperature mapping.
  
  

What you'll bring

• Bachelor's degree in Engineering, Life Sciences, or related field.
  
  
• 2–5 years' experience
  in temperature mapping within GMP/GDP environments.
  
  
• Strong knowledge of
  GDP & ALCOA principles
  .
  
  
• Experience with
  Kneat
  for protocols and reports (preferred).
  
  
• Confident in
  audit documentation
  and compliance requirements.
  
  

Validation Engineer – Laboratory Systems (CSV Focus)

What you'll do

• Lead
  Computer System Validation (CSV)
  activities for laboratory and analytical equipment.
  
  
• Draft and execute validation deliverables: URS, Risk Assessments, Test Scripts, IQ/OQ/PQ, Traceability.
  
  
• Ensure compliance with
  cGMP, 21 CFR Part 11, audit trails, and data integrity
  standards.
  
  
• Support integration of instruments with PCs, networks, and enterprise systems.
  
  
• Prepare/review SOPs, validation documentation, and lifecycle deliverables.
  
  

What you'll bring

• Bachelor's degree in Engineering, Computer Science, Life Sciences, or related field.
  
  
• 5–10 years' CSV experience
  with laboratory/analytical instruments.
  
  
• Strong knowledge of
  21 CFR Part 11, audit trails, data integrity, Windows OS
  .
  
  
• Exposure to
  microbiology analytical equipment
  (advantageous).
  
  
• Experience with
  Kneat validation management system
  (preferred).
  
  

Why Join

• Exciting roles within
  GMP-regulated environments
  .
  
  
• Work with cross-functional teams (QA, QC, IT, Engineering).
  
  
• Gain exposure to
  audit-ready projects
  with high regulatory standards.
  
  

Apply now if you have the right validation background and want to be part of cutting-edge CQV projects in Singapore.