James Lim is a seasoned professional in regulatory affairs and quality control with extensive experience in the biotechnology and pharmaceutical sectors. Currently serving as a Sr CMC Regulatory Affairs Specialist at Regeneron since November 2023, James previously held the position of Manager in QC Materials Technical Support CAR T at Bristol Myers Squibb from April 2019 to November 2023, where responsibilities included leading a team to develop critical documentation for the BMS Cell Therapy Network. James's earlier roles include significant contributions to Halo Pharmaceutical, Inc. as a Scientist/Technical Writer, and to MicroDose Therapeutx as an Associate Scientist II, focusing on analytical development and product evaluation. James initiated a career at Merck as an intern in medicinal chemistry and began analytical work at Chemtech Consulting. Academic credentials include a BS in Chemistry from Kean University and an ongoing Master's in Organic Chemistry from Rutgers University.
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