With over 14 years of experience in the pharmaceutical industry, I have defined and implemented cleaning validation strategies across various pharmaceutical environments. My career began in France with a leading pharmaceutical company, specializing in cleaning validation and compliance within biologics drug substance manufacturing. Later, as a consultant in Switzerland, I supported multiple organizations with diverse technologies in developing robust cleaning validation strategies.
For the past year and a half, I have led cleaning and cleaning validation activities for internal and external projects, focusing on innovation and regulatory compliance to meet customer needs. Additionally, I am an active member of the A3P working group on Annex 1, contributing to industry best practices in sterile manufacturing.
