Jason Lu is an accomplished Validation Engineer Principal at Sanofi Genzyme, with extensive experience in cleaning validation and related activities for drug product formulation and medical device manufacturing. Prior roles include Senior Validation Engineer at Barry-Wehmiller Design Group, where Jason wrote and executed cGMP documentation, and a Consultancy position at AveXis, Inc., providing commissioning and qualification support for biotech equipment. Jason also contributed to compliance at Celgene as an Equipment Qualification Consultant and led cleaning validation studies at Amgen. With a strong educational background, including a Master’s in Pharmaceutical Engineering from New Jersey Institute of Technology and a Bachelor’s in Chemical Engineering from Rutgers University, Jason demonstrates a robust commitment to quality in the pharmaceutical and biotech industries.
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