Payal Prajapati

About Payal Prajapati

I am a Quality and Microbiology professional with experience supporting cGMP-regulated pharmaceutical manufacturing, particularly in sterile injectable environments. Currently, I work as a Quality Assurance Chemist at Navinta Inc, where I support microbiological quality systems including environmental monitoring, endotoxin, MLT, and sterility testing oversight, contamination control, and laboratory data review to ensure compliance with FDA cGMP and USP standards.My role involves working closely with QC, manufacturing, validation, and engineering teams to maintain aseptic manufacturing controls. I participate in environmental monitoring trending, deviation and OOS investigations, CAPA implementation, and preparation of quality documentation such as SOPs and laboratory procedures while ensuring adherence to ALCOA+ data integrity principles.I also hold a Master’s degree in Regulatory Affairs from Northeastern University, where I developed knowledge in regulatory strategy, FDA submissions, and global compliance frameworks. With a foundation in quality systems, microbiology, and regulatory science, I am interested in opportunities that contribute to product quality, regulatory compliance, and patient safety.

Experience

1. Quality Assurance Chemist

   Navinta Iii Inc

   Oct 2024 — Present · Boca Raton, FL, US

Education

• Northeastern University

  Master's degree, Pharmacy Administration and Pharmacy Policy and Regulatory Affairs

• Uka Tarsadia University

  Bachelor's degree, Biotechnology

• Uka Tarsadia University

  Master's degree, Biotechnology