Cédric Pouzet

I am a biotechnology consultant specialized in GMP compliance and regulatory requirements, with hands-on experience in highly regulated pharmaceutical and biotech environments. I support companies in setting up, optimizing, and maintaining quality systems aligned with international standards.

My expertise covers Quality Assurance (QA), regulatory compliance (FDA / EMA), analytical development, and bioanalytical methods, including flow cytometry. I have extensive experience preparing and reviewing technical and regulatory documentation such as SOPs, validation protocols, analytical reports, and audit readiness packages.

In addition to my regulatory and analytical background, I have acted as a senior unit leader, coordinating multidisciplinary teams and ensuring operational excellence under GMP constraints. I also develop automated Excel and VBA-based reporting tools to improve data integrity, reduce manual errors, and streamline regulatory reporting processes.

I typically support projects such as GMP gap analysis, audit preparation, documentation structuring, analytical method development, and temporary QA/RA support. I work efficiently in both French and English and can adapt to short-term or long-term assignments.

This type of project is particularly motivating to me, and I am always keen to contribute my expertise to impactful and high-quality scientific and regulatory initiatives.