Experience in regulatory submissions; drug product life cycle management; export labeling requirements; clinical study compliance; and global procurement for RD; and working with ISI Toolbox, Rosetta Viewer, TRS Viewer, Credo, Liquent I.P, Lorenz eValidator, Pragmatic Validator, and Docubridge. Relocation and travel to various unanticipated locations within USA possible. Employer will accept suitable combination of education, training or experience.
Categories: eb3
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