Lifecycle Regulatory Lead – Ophthalmic Pharmaceuticals

A leading pharmaceutical and medical device company in Auvergne-Rhône-Alpes is seeking a Technical Regulatory Lead with a focus on Life Cycle Management. This role involves creating and maintaining regulatory files to support Marketing Authorisations, ensuring compliance with health authority regulations, and collaborating with cross-functional teams. The ideal candidate will have a Degree in a scientific discipline and extensive experience with marketing authorisation dossiers. Strong knowledge of sterile products and health authority engagements (FDA & EMA) is essential.

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