CQV Project Engineer - Life Sciences, GMP, Automation

ANTAES ASIA PTE. LTD.; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A leading Life Sciences consultancy in Singapore is seeking a professional with CQV experience to contribute to Life Science projects. The candidate will be responsible for developing and executing C&Q documentation, supporting the qualification of process and utility systems, and resolving technical issues. A Bachelor's degree in a relevant engineering field and 3-7 years of industry experience are required. The role emphasizes collaboration with multiple teams and adherence to strict GMP standards.

Qualifications

• 3–7 years of CQV experience in the pharmaceutical industry.
• Strong understanding of GMP, GEP, and FDA/EMA validation expectations.
• Experience in process equipment qualification and clean utilities.

Responsibilities

• Develop and execute C&Q documentation including commissioning protocols.
• Support end-to-end C&Q lifecycle for process and utility systems.
• Troubleshoot and resolve technical issues during C&Q execution.

Skills

GMP understanding

Documentation management

Strong communication

Risk-based CQV approach

Education

Bachelor’s Degree in Chemical, Mechanical, Biomedical Engineering

Tools

Veeva

Job description

A leading Life Sciences consultancy in Singapore is seeking a professional with CQV experience to contribute to Life Science projects. The candidate will be responsible for developing and executing C&Q documentation, supporting the qualification of process and utility systems, and resolving technical issues. A Bachelor's degree in a relevant engineering field and 3-7 years of industry experience are required. The role emphasizes collaboration with multiple teams and adherence to strict GMP standards.