About me
Simge Baloglu, PhD, is an Analytical Development and Quality Control leader with over 20 years of experience in biologics, gene and cell therapy, and vaccines. She has led analytical and CMC strategies from discovery through commercialization, regulatory approval, and lifecycle management. As SVP at Bluerock Therapeutics, she oversees 80+ scientists in Analytical Sciences and QC, ensuring regulatory compliance and product continuity. An expert in ICH guidelines and cGMP requirements, she has authored regulatory submissions, led global collaborations, and managed analytical programs across multiple therapeutic areas.
