Lisa Rose has over 30 years of manufacturing and quality experience in the pharmaceutical industry, demonstrating strong attention to detail and a commitment to mentoring team members. They served as a QA Supervisor at NBTY and Par Specialty Pharmaceuticals from 2014 to 2019, where they supervised staff and ensured compliance with industry standards. Currently, Lisa is the Quality Investigation Manager at BioStem Technologies and has held roles as a Senior External Quality Specialist at Moderna and Lead Deviation Investigator at Resilience. Throughout their career, they have focused on leading by example and helping teams achieve their full potential.
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