Natasha Madhow has worked in the Quality Assurance and Quality Control fields for nearly a decade. Natasha began their career in 2011 as a PQC Analyst for Sanofi, followed by a role as a Product Complaint Investigator and Quality Assurance Compliant Investigator at Otsuka Pharmaceutical Companies (U.S.) from 2013 to 2017. In 2017, they joined Clinical Genomics as a Quality Manager and Quality Assurance Engineering, serving as the Management Representative for Global Quality System (ISO 13485 and 21 CFR Part 820). Natasha reviewed and approved NCR, CAPA, and Deviations. Most recently, they returned to Sanofi-aventis as a PQC Analyst.
Natasha Madhow has attended Rutgers University - Newark.
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