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Jo helps clients by performing gap analysis of their drug manufacturing processes, and troubleshoots potential issues present in the quality management system of a drug manufacturer.
Prior to joining Parexel, Jo was a CMC reviewer and inspection investigator at the FDA, as Acting Branch Chief and Acting Quality Assessment Lead in CDER/OPQ. She has significant R&D experience in complex drug delivery, drug-device combination product, cell/tissue therapy, BioMEMS manufacturing.
Jo holds a PhD in Biomedical Engineering from the Johns Hopkins School of Medicine (USA) and a BS in Chemical Engineering and Biomedical Engineering from MIT (USA).
We are always available for a conversation.