Senior Validation Engineer - GMP/GAMP, IQ/OQ/PQ

ALLEGIS GROUP SINGAPORE PRIVATE LIMITED; Singapore; On-site; SGD 70,000 - 110,000; Full time

Job summary

Allegis Group Singapore Pte Ltd in Tuas, Singapore is seeking an experienced Validation Engineer to independently lead validation activities for equipment, processes, and computerised systems within a pharmaceutical manufacturing environment.

The role requires hands-on IQ/OQ/PQ, process and cleaning validation, and strong GMP/GAMP knowledge, with a focus on audit readiness, risk assessments, CAPA, and cross-functional collaboration.

Qualifications

• Degree in Engineering, Life Sciences, Pharmaceutical Sciences, or related discipline.
• 4–8 years of validation experience in pharma/regulated manufacturing.
• Hands-on IQ/OQ/PQ, process validation, cleaning validation and computerised system validation.
• Strong knowledge of GMP, GAMP, validation lifecycle management and regulatory requirements.
• Experience investigating deviations and supporting CAPA activities.
• Strong analytical, documentation and stakeholder management skills.

Responsibilities

• Develop, execute, and review validation protocols including IQ, OQ, and PQ.
• Perform process validation, cleaning validation, and computerized system validation activities.
• Author validation reports and ensure accurate documentation of validation outcomes.
• Lead validation risk assessments and implement mitigation strategies.
• Coordinate validation activities with QA, Engineering, Manufacturing, and other stakeholders.
• Maintain and update Validation Master Plans (VMP) and provide audit support.

Skills

IQ/OQ/PQ experience

Process validation

GMP knowledge

GAMP knowledge

Documentation

Stakeholder management

Education

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

Tools

Validation software systems

Job description

Allegis Group Singapore Pte Ltd in Tuas, Singapore is seeking an experienced Validation Engineer to independently lead validation activities for equipment, processes, and computerised systems within a pharmaceutical manufacturing environment.

The role requires hands-on IQ/OQ/PQ, process and cleaning validation, and strong GMP/GAMP knowledge, with a focus on audit readiness, risk assessments, CAPA, and cross-functional collaboration.