ÂÜÀòÂÒÂ×

Mehwish Khan has held various positions in the biotechnology field since 2006. Mehwish began their career at Tengion Inc. /Tragacept Inc. as a GMP Research Associate, where they were responsible for performing GMP manufacturing of Human Neo-bladder for phase II clinical trials. In 2010, they joined RMCC, Wake Forest Institute for Regenerative Medicine as a GMP Lead Manufacturing Associate, providing training to work in ISO 8 and ISO 7 classified areas. In 2018, they joined Precise Bio as Quality Manager and Site Lead, where they established and managed the QA department, QC lab, and the GLP manufacturing lab, as well as submitting pre-INDs and INDs.

Mehwish Khan obtained their Regulatory Affairs Certification (RAC) from the Regulatory Affairs Professional Society (RAPS) in 2020. Mehwish earned a Bachelor of Science (BS) in Biotechnology with a minor in Chemistry from Winston-Salem State University in 2016-2017. Prior to that, they obtained an Associate of Science (AS) in Biotechnology from Forsyth Technical Community College in 2005-2007.