Senior Validation Engineer

EFOR; Singapore; On-site; SGD 90,000 - 120,000; Full time

Benefits offered by this job

Generous Leave Policy

Health & Wellness Coverage

Professional Development Opportunities

Inclusive Culture

Job summary

EFOR in Singapore is seeking a validation professional to support commissioning and qualification (C&Q) activities for ongoing capital projects, along with cleaning validation, maintenance, and equipment qualification. You will act as a technical resource, delivering validation expertise across systems throughout their lifecycle in a GMP-regulated environment.

This hands-on role requires collaboration with Engineering, Quality, and Operations, protocol development, and documentation review.

Qualifications

• Bachelor's degree in Engineering, Life Sciences, or related discipline.
• Minimum 5 years of validation/C&Q experience in GMP-regulated pharma/biopharma.
• Solid understanding of equipment qualification and cleaning validation.
• Familiarity with validation lifecycle documentation (protocols, test plans, reports).
• Strong communication skills to guide cross-functional teams.

Responsibilities

• Support C&Q activities for ongoing capital projects, including protocol development and documentation.
• Assist routine cleaning validation to ensure GMP compliance.
• Provide technical advice and validation support to project teams.
• Support equipment qualification and CTC qualification activities.
• Review validation documentation for GMP alignment.
• Collaborate with Engineering, Quality, and Operations to deliver validation deliverables.
• Undertake other validation-related activities as assigned.

Skills

Validation experience

Cross-functional collaboration

Communication skills

GMP knowledge

Education

Bachelor's degree in Engineering/Life Sciences

Job description

This role will support commissioning and qualification (C&Q) activities for ongoing capital projects, alongside routine cleaning validation, periodic maintenance, and equipment/CTC qualification activities. The successful candidate will act as a technical resource to the wider project team, providing validation expertise across systems and equipment throughout their lifecycle. This is a hands-on role suited to a validation professional who is comfortable working across both project-based and routine validation activities in a GMP-regulated environment.

Key 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

Required 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
• Generous Leave Policy.
• Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs.
• Professional Development Opportunities: Access continuous learning programs and resources for career growth within the company.
• Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated.
• Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career.