Ritika Grover

Ritika Grover is a Senior Manager in Quality and Regulatory Affairs with over 15 years of expertise in quality assurance and compliance management. They have demonstrated significant leadership by spearheading expedited FDA approval processes for Pfizer’s COVID-19 vaccine and coordinating approvals for Paxlovid. Ritika has managed teams to achieve strategic objectives while overseeing compliance initiatives and serving as a quality assurance representative in audit responses. They hold a Bachelor of Science in Biochemistry and Molecular Biology from Michigan State University.