Process Validation Engineer - Pharma (12-Month Contract)

Manpower Singapore; Singapore; On-site; SGD 91,000 - 109,000; Full time

Job summary

A Fortune 500 global biopharmaceutical company is seeking a Validation Engineer to support process and cleaning validations on a 12-month contract located in Tuas, Singapore. The role focuses on IQ/OQ/PQ, process validation and report writing.

You will lead risk assessments, ensure GMP/GAMP compliance, investigate deviations and support CAPA, coordinating with QA, Engineering and Manufacturing. Requirements include a degree in Engineering or Life Sciences and 4–8 years of validation experience

Qualifications

• 4–8 years of validation experience in pharmaceutical/biotech manufacturing.
• Experience with IQ/OQ/PQ, cleaning validation, and process validation.

Responsibilities

• Develop and execute validation protocols (IQ/OQ/PQ, process validation, cleaning validation) and author final reports.
• Lead validation risk assessments and ensure GMP/GAMP compliance.
• Investigate validation-related deviations and support CAPA implementation.
• Coordinate validation activities with QA, Engineering, and Manufacturing.
• Maintain and update validation master plans.

Skills

GMP knowledge

Validation mindset

Cross-functional collaboration

Education

Degree in Engineering or Life Sciences

Job description

A Fortune 500 global biopharmaceutical company is seeking a Validation Engineer to support process and cleaning validations on a 12-month contract located in Tuas, Singapore. The role focuses on IQ/OQ/PQ, process validation and report writing.

You will lead risk assessments, ensure GMP/GAMP compliance, investigate deviations and support CAPA, coordinating with QA, Engineering and Manufacturing. Requirements include a degree in Engineering or Life Sciences and 4–8 years of validation experience