Validation Engineer

Novexx Pte Ltd; Singapore; On-site; SGD 80,000 - 100,000; Full time

Job summary

A leading validation consultancy is looking for an expert to contribute to validation planning and manage DQ documentation in Singapore. The successful candidate will prepare and evaluate validation protocols while serving as the main validation representative for various project teams. This role requires strong problem-solving skills and effective coordination with internal stakeholders and external partners.

Qualifications

• Expertise in writing and managing DQ documentation such as URS, FMEA, PVP.
• Experience in validation planning and execution.
• Ability to engage with internal and external stakeholders.

Responsibilities

• Contribute to validation planning and assist with medium-to-large scale projects.
• Prepare, execute, and evaluate validation protocols and documentation.
• Serve as the main validation representative for project teams.

Skills

Validation expertise in pharmaceutical plant

Risk assessments

Troubleshooting

Cross-organizational coordination

Job description

Contributes to validation planning and assists with carrying out medium‑to large‑scale projects that require customized, risk‑based execution strategies, problem investigations, and troubleshooting while meeting project timelines.

Utilizes expertise and input from Subject Matter Experts to perform effective risk assessments and develop experimental designs for project tasks.

Prepares, executes, and evaluates validation protocols and associated documentation in alignment with company policies and procedures, including (but not limited to) FMEA, URS, PVP.

Serves as the main validation representative for the project team, acting as the primary point of contact for validation‑related aspects of contracts and projects.

Engages with internal stakeholders and external partners on significant validation issues that may require cross‑organizational coordination.

Collaborates with technical support teams to perform qualification tests and engineering studies.

Adheres to all applicable regulations and standards related to Quality, Environmental, Health, Safety, and Energy (EHS&E) Global Policies, Engineering Standards, and other relevant governance requirements.

Requirements:

Validation expertise in pharmaceutical plant and managing DQ documentation URS/FMEA/PVP