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The role will provide scientific and technical leadership for analytical development at various stages of drug development both internal and external through CDMO with particular emphasis on research and early development (pre-DP0) including material
You will lead Major Global QA Medical Device projects, and you will support the Ferring Manufacturing sites as main point of contact regarding Medical Devices and device constituents of combination/medicinal products. Contribute to QMS improvements
You will serve as the global technical authority for our CMVD Single-Pill Combination (SPC) portfolio. You will lead a team of Subject Matter Experts (SMEs) to ensure the seamless commercialization, scale-up, and lifecycle management of complex OSD