Prepare the respective quality CMC documentation in close collaboration with regulatory affairs, local CMC contacts or subject matter experts (e.g. quality control, production, etc.) * On-time delivery of documents and contents aligned with RA CMC processes and templates for existing global pharmaceutical products (i.e. tech documents required for variations, geographical extensions and renewals) * Several years of industry experience in either pharmaceutical development or production, chemical development, analytical sciences, quality control, quality assurance or regulatory affairs
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