CSV Validation Engineer (Contract)

No deviation; Singapore; On-site; SGD 70,000 - 110,000; Full time

Benefits offered by this job

Leave Policy

Health & Wellness Coverage

Professional Development

Inclusive Culture

Career Growth

Job summary

No Deviation is seeking a Validation Engineer (CSV) to support DeltaV systems, develop and review validation protocols (IQ/OQ/PQ), and ensure regulatory compliance across the validation lifecycle.

You will collaborate with engineering and QA teams, perform risk assessments, maintain audit-ready documentation, and contribute to GMP-regulated projects with a focus on quality, integrity, and patient safety. This role offers growth in a dynamic, inclusive pharma consultancy.

Qualifications

• Experience with DeltaV validation, coding/configuration preferred.
• Familiarity with CSV lifecycle and GAMP 5 guidelines.
• Strong documentation and review skills; capable of audit-ready records.

Responsibilities

• Develop and review CSV protocols (IQ/OQ/PQ) for DeltaV systems.
• Support configuration and validation of DeltaV automation systems.
• Ensure compliance with GAMP 5 and regulatory guidelines.
• Perform risk assessments and system impact assessments.
• Review system design specifications and functional documents.
• Coordinate testing activities and resolve validation issues.
• Maintain proper documentation for audit readiness.

Skills

DeltaV

CSV lifecycle

GAMP 5

GMP

Documentation

Stakeholder management

Education

Degree in Engineering, IT, or related discipline

Job description

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

The Validation Engineer (CSV) supports computer system validation activities, with a focus on DeltaV systems. The role involves protocol development, review, and ensuring systems are compliant with regulatory requirements throughout the validation lifecycle.

Key Responsibilities

• Develop and review CSV protocols (IQ/OQ/PQ) for DeltaV systems.
• Support configuration and validation of DeltaV automation systems.
• Ensure compliance with GAMP 5 and regulatory guidelines.
• Perform risk assessments and system impact assessments.
• Review system design specifications and functional documents.
• Coordinate testing activities and resolve validation issues.
• Maintain proper documentation for audit readiness.

Required Qualifications

• Degree in Engineering, IT, or related discipline.
• Experience with DeltaV systems (coding/configuration preferred).
• Knowledge of CSV lifecycle and GAMP 5 guidelines.
• Familiarity with GMP‑regulated environments.
• Strong documentation and review skills.
• Good communication and stakeholder management skills.

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.

How To Apply

Are you ready to play a key role in shaping the future of pharmaceutical solutions? If you’re passionate about making an impact, we want you on our team! Please submit your resume, outlining your qualifications and experience relevant to the role, here.