CQV Engineer — GMP Equipment Validation & Handover Lead

A pharmaceutical consultancy firm in Singapore seeks a Project CQV Engineer to handle commissioning and qualification activities for GMP equipment. The ideal candidate will have a degree in Engineering and 2–8 years of relevant experience. Key responsibilities include executing validation activities, coordinating with vendors, and ensuring compliance with regulatory requirements. Join us to make a difference in the pharmaceutical industry while advancing your career in a collaborative environment.
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