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Tunnell Government Services

Medical Officer - Plastic Surgeon

Physicians & SurgeonsConfirmed live in the last 24 hours
Full-timeBethesda, MD, USANo salary listed

About the Job

Requirements

  • The candidate must possess a Doctor of Medicine (M.D. or equivalent) from an accredited medical school in the United States.
  • The candidate must possess a current, active, full, and unrestricted medical license or registration as a Physician to practice medicine in a State, District of Columbia, the Commonwealth of Puerto Rico, or a territory of the United States.
  • At least ten years of relevant clinical experience is required.
  • Certification from a relevant U.S. specialty board organization, such as the American Board of Plastic Surgery, is required.
  • The candidate must have a thorough understanding of current clinical practices in plastic surgery, including diagnosis and treatment, and current and emerging trends in practice.
  • The candidate must be an expert in the function and utilization of medical devices commonly used in plastic surgery, including aesthetic and body contouring devices, precision cutting and dissection tools, microsurgical equipment, breast and implant-related tools, craniofacial and bone tools, non-invasive diagnostic devices and instruments, invasive devices such as implantable devices, and surgical systems.
  • The candidate must communicate effectively with others through written and verbal communication.
  • The candidate must be able to work independently and within a team of technical personnel.
  • The candidate must be a United States citizen or a full Green Card holder.

Responsibilities

  • Provide expert consulting services to assist the FDA Center for Devices and Radiological Health with its regulatory responsibilities.
  • Support medical device reviews for EUA, 510(k), PME, De Novo marketing applications, and pre-submissions.
  • Participate in meetings and teleconferences.
  • Coordinate meetings with internal and external stakeholders.
  • Develop written reviews and correspondence.
  • Perform research and conduct data analysis.
  • Write detailed documents and reports.
  • Execute administrative office tasks related to CDRH projects.

Desired Qualifications

  • Familiarity with FDA medical device regulatory processes, regulations such as 21 CFR Part 878 (General and Plastic Surgery Devices), and related guidance is preferred.

About the Company

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