CQV Engineer - Pharma Quality & Compliance

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

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