Judith Simonot

Regulatory Affairs and Biological Safety Process Validation Project Manager at In2Bones

Judith Simonot has a diverse work experience in the medical industry. Judith has worked as a Regulatory Affairs and Biological Safety Process Validation Project Manager at In2Bones since 2019. Prior to that, they worked at LDR M\u00e9dical (Zimmer Biomet) from 2013 to 2019, where they held various roles including R&D Project Manager and Design Control Engineer R&D. At LDR M\u00e9dical, they were responsible for tasks such as analyzing field returns, managing line extensions, analyzing customer complaints, conducting post-market surveillance, and managing design and process changes. Judith also worked as a Stagiaire - Charg\u00e9e de suivi des dossiers de conception at LDR Medical in 2013, where they performed clinical evaluations and updated Device History Files. Additionally, they completed a internship at Centre d'Investigations Cliniques et d'Innovations Technologiques (CIC-IT) in 2012 and worked as an R&D Engineer at Biotika in the same year. Judith also had a brief internship at CHU Jean Minjoz in 2012.

Judith Simonot completed their education with a Bachelor's degree in the field of study in "Scientifique" from Lycée Louis Aragon in 2008. Following that, they attended Prépa BCPST Lycée Jean Rostand Strasbourg from 2008 to 2010, however, no degree was mentioned for this period. Finally, Judith obtained a Diplôme d'ingénieur in Biomedical/Medical Engineering from ISIFC in 2013.

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