LSI
Tessa Seka is a biomedical engineer specializing in medical devices, holding a degree from ISIFC. Currently serving as an Ingénieure consultante en Affaires Réglementaires, Qualité, R&D et Affaires Clinique at LSI since October 2022, Tessa focuses on updating design dossiers and technical documentation for ophthalmology devices, as well as clinical evaluation reports for dental implants. Previous experience includes roles as a regulatory affairs intern at Cerba Research, where Tessa contributed to clinical performance validation and study setup, and as an engineer in regulatory affairs at Stratégie Industrielle ISIFC, ensuring compliance with EU regulations. Tessa has also worked on developing clinical investigation plans and has experience in strategic industrial consulting within the biomedical sector.
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