Senior Validation Engineer – GMP/GAMP (Pharma)

Allegis Group Singapore Pte Ltd; Singapore; On-site; SGD 90,000 - 140,000; 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 focuses on ensuring GMP and GAMP compliance, supporting quality, operational excellence, and regulatory readiness while collaborating across Quality Assurance, Engineering and Manufacturing teams.

Qualifications

• 4–8 years of validation experience in pharmaceutical 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.
• Excellent documentation and stakeholder management skills.

Responsibilities

• Lead validation activities for equipment, processes and computerised systems.
• Develop, execute and review validation protocols including IQ, OQ, PQ.
• Author validation reports and ensure compliant documentation.
• Coordinate validation activities with Quality Assurance, Engineering and Manufacturing.
• Support audits, inspections and regulatory assessments.

Education

Degree in Engineering, Life Sciences, Pharmaceutical Sciences, or a related discipline

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 focuses on ensuring GMP and GAMP compliance, supporting quality, operational excellence, and regulatory readiness while collaborating across Quality Assurance, Engineering and Manufacturing teams.