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CQV Project Engineer - Life Sciences, GMP, Automation
Résumé du poste
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.
Responsabilités
- 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.
Connaissances
Formation
Outils
* Le salaire de référence se base sur les salaires cibles des leaders du marché dans leurs secteurs correspondants. Il vise à servir de guide pour aider les membres Premium à évaluer les postes vacants et contribuer aux négociations salariales. Le salaire de référence n’est pas fourni directement par l’entreprise et peut pourrait être beaucoup plus élevé ou plus bas.