Delphine Vast

I am an independent consultant specializing in analytical validation, microbiology, and GMP documentation, with a PhD in science and 5 years of experience at Merck (Martillac) in a pharmaceutical environment.

I support biotech, pharma, and CDMO companies in drafting and reviewing critical quality documents: validation protocols, GMP reports, CMC documentation, SOPs, and regulatory compliance deliverables.

My expertise covers sterile environments, analytical method validation (microbiology and bioanalysis), and GMP requirements (data integrity, compliance, audits).

I work primarily remotely with QA, QC, and R&D teams, bringing strong scientific rigor and a field understanding of industrial requirements.