Description
The Project Manager III creates and manages project schedules for technical documentation, instructions for use (IFU), user manuals, localization, regulatory submissions, and international product rollouts for medical and non-medical devices. The role coordinates technical writers, localization specialists, regulatory, quality, engineering, clinical development, human factors, marketing, training, procurement, and external translation and print vendors, while managing risks, resources, deadlines, design control, and process improvements. The posting lists preferred experience, education, and certifications, and requires strong communication, organizational, analytical, and project-management skills.
