Senior Validation Engineer | GMP Compliance & IQ/OQ/PQ

TEKsystems; Singapore; On-site; SGD 90,000 - 130,000; Full time

Job summary

Allegis Group Singapore Pte Ltd seeks an experienced Validation Engineer to lead validation activities for equipment, processes, and computerised systems in a pharmaceutical manufacturing environment. You will ensure GMP and GAMP compliance while supporting quality, operational excellence, and regulatory readiness.

The role encompasses IQ/OQ/PQ, process and cleaning validation, and validation documentation.

Qualifications

• Must have GMP/GAMP knowledge and experience in pharmaceutical validation.
• Experience with IQ/OQ/PQ, process validation, cleaning validation, and computerised system validation.
• Strong documentation and audit-readiness mindset required.

Responsibilities

• Lead validation management for equipment, processes, and computerised systems.
• Perform risk assessment and ensure compliance with GMP, GAMP, and regulatory requirements.
• Investigate deviations, support CAPA, and drive continuous improvement.
• Coordinate validation activities with QA, Engineering, and Manufacturing; maintain Validation Master Plan.

Skills

GMP knowledge

GAMP knowledge

Stakeholder management

Documentation

Analytical skills

Education

Bachelor's degree in Engineering, Life Sciences, Pharmaceutical Sciences

Tools

Validation software systems

Job description

Allegis Group Singapore Pte Ltd seeks an experienced Validation Engineer to lead validation activities for equipment, processes, and computerised systems in a pharmaceutical manufacturing environment. You will ensure GMP and GAMP compliance while supporting quality, operational excellence, and regulatory readiness.

The role encompasses IQ/OQ/PQ, process and cleaning validation, and validation documentation.