3-7 years cqv experience in pharmaceutical industry
Bachelor's degree in engineering field
Strong understanding of gmp and gep standards
Antaes Asia PTE. LTD. is seeking a CQV Engineer to contribute to Life Science projects by managing the commissioning and qualification lifecycle for various systems and processes. The ideal candidate will possess 3–7 years of relevant experience and a strong understanding of GMP standards
Job Summary
The role involves developing and executing comprehensive CQV documentation including IQ/OQ/PQ protocols and traceability matrices for life science projects.
Candidates will support the end-to-end qualification lifecycle for process equipment, clean utilities, and automation systems like DeltaV and SCADA.
The position requires ensuring all deliverables meet internal Quality standards and align with the site Validation Master Plan while coordinating with vendors.
Matching Summary
Match Score: 85
Antaes Asia PTE. LTD. is seeking a CQV Engineer to contribute to Life Science projects by managing the commissioning and qualification lifecycle for various systems and processes. The ideal candidate will possess 3–7 years of relevant experience and a strong understanding of GMP standards.
Skills & Requirements
Must-have
3-7 years CQV experience in pharmaceutical industry
Bachelor's Degree in Engineering field
Strong understanding of GMP and GEP standards
Experience with bioreactors and chromatography skids
Proficiency with Veeva documentation management systems
Nice-to-have
Highly motivated to work independently
Excellent oral and written communication skills
Ability to collaborate with cross-functional teams
Familiarity with risk-based CQV approach
Key Requirements
Bachelor's Degree in Chemical, Mechanical, or Biomedical Engineering
3–7 years of CQV experience in pharmaceutical industry
Proficiency with Veeva documentation management systems