Validation Engineer - Process/ Pharma/ 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

Validation Engineer - Process/ Pharma/ Contract

12 Months Contract

Location : Tuas

Industry: BioPharmaceutical

Salary Up to $9,000 depending on experience

Our client is a Fortune 500 global biopharmaceutical company committed to improving lives through innovation. With a diverse pipeline across immunology, oncology, neuroscience, eye care, and aesthetics, our client offers diverse career opportunities.

Key Responsibilities

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

Requirements

• Minimum 4 - 8 years' experience with Degree in Engineering, Life Sciences, or related field.
• 4-8 years of validation experience in pharmaceutical/biotech manufacturing.