Job Description :
Local candidate needed to sit on site in Memphis:
1800 Pyramid Place Memphis, TN 38132
Responsibilities may include the following and other duties may be assigned: Directs or performs coordination and preparation of document packages for regulatory submissions supporting EU Medical Device Regulation (MDR Leads or compiles all materials required in submissions for EU MDR. Recommends changes for labeling, manufacturing, marketing, and clinical protocol for regulatory compliance. Monitors and improves tracking / control systems. Keeps abreast of regulatory procedures and changes.
SPECIALIST CAREER STREAM: Typically an individual contributor with responsibility in a professional discipline or specialty. Delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals.
DIFFERENTIATING FACTORS
Autonomy: Entry level individual contributor on a project or work team. Works with close supervision.
Organizational Impact: Delivers work of limited scope, typically smaller, less complex projects or related activities.
Innovation and Complexity: Identifies, defines and addresses problems that are not immediately evident but typically not difficult or complex. Makes minor changes in systems and processes to solve problems .
Communication and Influence: Communicates primarily with internal contacts within immediate group. Contacts others to gather, confirm and convey information.
Leadership and Talent Management: N / A job at this level is focused on self development . Required Knowledge and Experience: Requires broad theoretical job knowledge typically obtained through advanced education.
Requires a University Degree, 0 years of experience required.