Senior Molecule Quality Lead - GMP & Early-Phase

A biotechnology firm is seeking a Senior Principal Associate to oversee GMP operations, ensuring compliance during startup and steady-state operations. The ideal candidate will have a BA/BS degree in Engineering, Science, or related field, with a minimum of 5 years of experience in the biotech or pharmaceutical industry. Strong skills in quality management and cross-functional collaboration are essential. This position is based in Lebanon, IN, with potential travel of 5% - 15%. On-call support may be required outside of normal working hours. #J-18808-Ljbffr