Senior Validation Engineer — GMP-CQV Expert

no deviation; Singapore; On-site; SGD 110,000 - 150,000; Full time

Benefits offered by this job

Generous Leave Policy

Health & Dental Coverage

Professional Development

Inclusive Culture

Career Impact

Job summary

No Deviation is seeking a Validation/CQV professional in Singapore to support commissioning and qualification activities for capital projects, cleaning validation, and equipment/CTC qualification. This hands-on role spans project-based and routine validation in GMP-regulated settings.

The candidate should hold a Bachelor's in Engineering or Life Sciences and have at least 5 years of validation/C&Q experience with strong documentation and collaboration skills.

Qualifications

• Bachelor's Degree in Engineering, Life Sciences, or a related discipline.
• Minimum 5 years of relevant experience in validation/C&Q within a GMP-regulated pharmaceutical or biopharmaceutical environment.
• Solid understanding of equipment qualification, cleaning validation, and periodic review processes.
• Familiarity with validation lifecycle documentation (protocols, test plans, reports).
• Strong communication skills with the ability to provide technical guidance to cross-functional teams.
• Meticulous, organized, and able to manage multiple validation activities concurrently.

Responsibilities

• Support C&Q activities for ongoing capital projects, including protocol development, execution, and documentation review.
• Support routine cleaning validation activities, ensuring compliance with site and regulatory requirements.
• Provide technical advice and validation support to the wider project team.
• Support routine periodic maintenance, equipment qualification, and Clean-in-Place/Temperature Control (CTC) qualification activities.
• Review and assess validation documentation to ensure alignment with GMP and internal quality standards.
• Collaborate cross-functionally with Engineering, Quality, and Operations to support validation deliverables.
• Undertake any other validation-related activities as assigned.

Skills

GMP experience

Validation/C&Q

Documentation skills

Communication skills

Organized

Education

Bachelor's degree in Engineering, Life Sciences, or related

Job description

No Deviation is seeking a Validation/CQV professional in Singapore to support commissioning and qualification activities for capital projects, cleaning validation, and equipment/CTC qualification. This hands-on role spans project-based and routine validation in GMP-regulated settings.

The candidate should hold a Bachelor's in Engineering or Life Sciences and have at least 5 years of validation/C&Q experience with strong documentation and collaboration skills.