3-7 years cqv experience in pharmaceutical industry
Bachelor's degree in engineering field
Proficiency with gmp, gep, and ispe baseline guides
Antaes Asia PTE. LTD. is seeking a Project Engineer to contribute to Life Science projects by managing commissioning and qualification (C&Q) activities, ensuring compliance with GMP standards, and collaborating with cross-functional teams. The ideal candidate should have a Bachelor’s degree in engineering and 3–7 years of relevant experience in the pharmaceutical industry
Job Summary
The role involves contributing to Life Science projects by developing and executing comprehensive Commissioning and Qualification documentation.
Candidates will manage the end-to-end C&Q lifecycle for critical systems such as bioreactors, WFI, HVAC, and automation platforms while ensuring GMP compliance.
The position requires close collaboration with Engineering, QA Validation, Manufacturing, and Automation teams to support system handover and training.
Matching Summary
Match Score: 85
Antaes Asia PTE. LTD. is seeking a Project Engineer to contribute to Life Science projects by managing commissioning and qualification (C&Q) activities, ensuring compliance with GMP standards, and collaborating with cross-functional teams. The ideal candidate should have a Bachelor’s degree in engineering and 3–7 years of relevant experience in the pharmaceutical industry.
Skills & Requirements
Must-have
3-7 years CQV experience in pharmaceutical industry
Bachelor's Degree in Engineering field
Proficiency with GMP, GEP, and ISPE Baseline Guides
Experience with bioreactors, chromatography, and clean utilities
Knowledge of DeltaV, PLC, and SCADA automation qualification
Nice-to-have
Highly motivated and able to work independently
Strong organizational and communication skills
Familiarity with risk-based CQV approach
Experience coordinating with cross-functional teams
Ability to promote Antaes services to clients
Key Requirements
Bachelor's Degree in Chemical, Mechanical, Biomedical, or related Engineering
3-7 years of CQV experience in pharmaceutical industry
Proficiency with documentation management systems like Veeva