Marilou has been an MSAT Process Engineer for almost 3 years at Oxford Biomedica, using her expertise to enable the introduction of new processes and technologies to Fill and Finish GMP manufacturing, driving robustness and continuous improvement throughout the product cycle of gene and cell therapy products. Before joining the UK, she worked as a consultant in Brussels as QA validation (GSK) and in several places in France as QA operational and Process Engineer (start-up and MSD). Visiting companies of different size, with different cultures and in charge of different roles has given her the opportunity to enlarge her knowledge about the pharmaceutical industry.
Check out the incredible speaker line-up to see who will be joining Marilou.
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