CQ Engineer

No deviation; Singapore; On-site; SGD 90,000 - 150,000; Full time

Benefits offered by this job

Generous Leave

Health & Wellness Coverage

Professional Development

Inclusive Culture

Impactful Work

Job summary

No Deviation is seeking a CQ Engineer to execute CQV activities ensuring cGMP compliance and data integrity, collaborating with cross‑functional teams from engineering to operations. You will develop and review plans, protocols, and reports, support risk assessments, and help ensure systems are validated before handover to operations.

The ideal candidate has a bachelor’s degree in engineering or science, 5+ years in pharmaceutical CQV, and strong communication skills to thrive in a dynamic

Qualifications

• Bachelor's degree in Engineering or Science.
• Minimum 5 years of Pharmaceutical/CVQ experience.
• Hands-on experience in manufacturing, laboratory, or utilities environments.
• Strong understanding of CSV, CSA, and 21 CFR Part 11 requirements.
• Experience with execution platforms (e.g., Kneat) is an advantage.
• Basic project management skills and ability to work independently.
• Strong communication and right-first-time mindset.
• Demonstrates accountability, adaptability, and willingness to grow into senior roles.

Responsibilities

• Prepare and support development of CQV documentation including plans, protocols, traceability matrices, and reports.
• Review vendor FAT/SAT documentation and support document lifecycle activities such as drafting and reviewing SOPs, specifications, and risk/integrity assessments.
• Participate in Change Evaluation (CE) and Change Control (CC) by identifying impacted systems, documents, and validated states.
• Support execution planning, including coordination with vendors and stakeholders.
• Perform system walkdowns and support commissioning activities (FAT and SAT).
• Execute qualification and validation activities in accordance with approved protocols and procedures.
• Ensure compliance with GxP, safety standards, and data integrity requirements.

Education

Bachelor's degree in Engineering or Science

Tools

Kneat

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

The CQ Engineer is responsible for executing commissioning, qualification, and validation (CQV) activities to ensure compliance with cGMP, regulatory, and company quality requirements. The role supports project delivery through risk-based CQV execution, development of high-quality documentation, and ensuring that systems are fit for their intended use prior to handover to operations. The position requires strong collaboration with cross‑functional stakeholders and adherence to safety, quality, and data integrity standards.

Key Responsibilities

• Prepare and support development of CQV documentation including plans, protocols, traceability matrices, and reports
• Review vendor FAT/SAT documentation and support document lifecycle activities such as drafting and reviewing SOPs, specifications, and risk/integrity assessments
• Participate in Change Evaluation (CE) and Change Control (CC) by identifying impacted systems, documents, and validated states
• Support execution planning, including coordination with vendors and stakeholders
• Perform system walkdowns and support commissioning activities (FAT and SAT)
• Execute qualification and validation activities in accordance with approved protocols and procedures
• Ensure compliance with GxP, safety standards, and data integrity requirements

Required Qualifications

• Bachelor's degree in Engineering or Science
• Minimum 5 years of experience in Pharmaceutical / Biopharmaceutical CQV
• Hands‑on experience in manufacturing, laboratory, or utilities environments
• Strong understanding of CSV, CSA, and/or 21 CFR Part 11 requirements
• Experience with execution platforms (e.g., Kneat) is an advantage
• Basic project management skills and ability to work independently
• Strong communication skills and a right-first-time mindset
• Demonstrates accountability, adaptability, and willingness to grow into senior roles

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.