Senior CQV Project Lead - GMP Validation

A leading pharmaceutical firm in Puerto Rico seeks a Senior CQV Project Manager to oversee CQV activities across manufacturing facilities. The role involves leading project execution from planning to final approval while ensuring regulatory compliance with guidelines such as cGMP and FDA. Candidates should have over 10 years of experience in the industry, possess strong leadership skills, and have a background in CQV lifecycle management. Knowledge of both English and Spanish is preferred for this role in Puerto Rico.
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