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Quality Assurance Specialist II @ Catalent

San Diego, California, United States of America, 92121OnsiteFull-timePosted 21 days ago

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About this role

Embrace the opportunity to become a Quality Assurance Specialist II and play a key role in ensuring compliance with cGMP and SOPs for clinical trial projects. Leverage your expertise in quality assurance, batch record review, and regulatory documentation to support innovative drug development in a dynamic, collaborative environment. Grow your career with a global pharmaceutical leader.. Category: Other

Skills

gmp compliancequality assurance processesdocument managementsop compliancedeviation writingchange controlmaterial managementerp systemsms officeclinical trial supportpharmaceutical qualityclient communicationpivot tablesvlookupexcel formulas

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Quality Assurance Specialist II at Catalent | ResuMinder Jobs