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Project Engineer: Responsibilities: * Manage multiple project activities across cross-functional and cross product teams. * Work with all relevant departments to ensure product development and manufacturing tasks are completed on schedule and meet specifications. * Develop, manage, and communicate project plans for assigned activities. * Support design and testing of new products as required. * Ensure that required regulatory project documentation, including design control procedures, are created and properly maintained for all assigned projects. * Provide guidance and support to other engineers to effectively execute projects on-time. * Assist in the development of Six Sigma driven project methodologies. * Assist with the development and maintenance of a Project Management Office (PMO). Qualifications: * A Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, Electrical Engineering, Bio Materials, or equivalent is required. * PMP Certification is a Plus. * A minimum of 7 years of experience, * Experience in medical product development is preferred. * Experience running multiple projects while managing other engineering resources running separate projects is essential. * Extensive experience in the design, development, and tolerance of complex medical products with continued exposure to the autoclave environment is a plus. * A working knowledge of applicable FDA and ISO standards is a plus. * A complete understanding medical device design control requirements is necessary. * Must be able to effectively manage multiple cross-functional product teams. * A working knowledge of basic Microsoft Applications including Word, Excel, Outlook, PowerPoint, and Project is required. * A working knowledge of the Solid Works design package is necessary. * Must be comfortable leading multidisciplinary teams in bringing a project from conception through market release and beyond. Contact Information Contact: chris sullivan Job Location: CT, Email: csullivan@natleng.com Phone:800-562-3493 Apply Online |