Senior Validation Engineer — GMP Biotech Systems

Biopharma Careers; Singapore; On-site; SGD 90,000 - 140,000; Full time

Job summary

Sanofi Tuas site seeks a Validation Engineer to implement and maintain qualification and validation strategies, plans, protocols and reports. You will ensure equipment, facilities, cleaning and disinfection are properly qualified and documented, coordinating with internal and external stakeholders.

The role reports to the Senior Manager, Validation and requires hands-on experience in GMP, biotech processes and validation lifecycle management, with a focus on continuous improvement and

Qualifications

• Bachelor’s degree in Engineering and 4+ years of related experience.
• Fluent in English (speaking and writing).
• Strong knowledge of GMP, validation concepts and biopharma processes.

Responsibilities

• Execute qualification and validation plans, protocols and reports with stakeholders.
• Ensure regulatory compliance and quality standards for validation.
• Validate equipment, cleaning, sterilization and disinfection processes and documentation.
• Lead investigations, assess root causes, and communicate mitigation actions.
• Drive continuous improvement in qualification lifecycle and use new technologies.

Skills

GMP knowledge

Validation

Analytical skills

Kneat

Team collaboration

Education

Bachelor's degree in Engineering

Tools

Kneat

Job description

Sanofi Tuas site seeks a Validation Engineer to implement and maintain qualification and validation strategies, plans, protocols and reports. You will ensure equipment, facilities, cleaning and disinfection are properly qualified and documented, coordinating with internal and external stakeholders.

The role reports to the Senior Manager, Validation and requires hands-on experience in GMP, biotech processes and validation lifecycle management, with a focus on continuous improvement and