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Michelle has 8 years of experience in the medical device and biotechnology industries. While at Ximedica, she is responsible for ensuring medical device development meets design control requirements for design verification and process validation activities. She has worked for clients such as Smiths Medical, Kimberly-Clark and Davol. Previous to joining Ximedica, Michelle was a development and process engineer in the biotechnology industry. She was involved in process transfer and FDA approval efforts associated with the launch of protein therapeutic medicines produced by mammalian cells.

Michelle graduated with a BSE in Chemical Engineering from the University of Michigan and a Masters in Chemical Engineering from the Massachusetts Institute of Technology.

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