Senior Validation Engineer

NO DEVIATION PTE. LTD.; Singapore; On-site; SGD 90,000 - 120,000; Full time

Benefits offered by this job

Leave policy

Health & dental

Professional development

Inclusive culture

Impactful work

Job summary

No Deviation Pte. Ltd. in Singapore seeks a validation professional to support C&Q activities for ongoing capital projects, routine cleaning validation, and equipment qualification. The role requires hands-on expertise across project-based and routine validation within a GMP-regulated environment.

The successful candidate will collaborate with Engineering, Quality, and Operations, ensuring documentation review and adherence to GMP standards while supporting maintenance and CTC qualifications.

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

Validation/CQV expertise

GMP knowledge

Cross-functional communication

Documentation writing

Education

Bachelor's Degree in Engineering or Life Sciences

Job description

About No deviation

At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful projects and drive innovation.

We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That's why we foster a culture of collaboration, inclusion, and continuous development - empowering our team members to grow personally and professionally.

Position Overview

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

Why join us?

• 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.