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Urgent! Validation Engineers – Temperature Mapping Job Opening In Tuas Mesa Stock Tank – Now Hiring TG Singapore

Validation Engineers – Temperature Mapping



Job description

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.


Required Skill Profession

Other General



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