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Tunnell Government Services

Orthopedic 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.
  • Certification from a relevant U.S. specialty board organization, such as the American Board of Orthopedic Surgery.
  • Thorough understanding of current clinical practices in orthopedic surgery, including diagnosis and treatment, and current or emerging trends in practice.
  • Expertise in the function and utilization of medical devices commonly used in orthopedic surgery, including permanent and temporary implants, prostheses, fixation devices, osteobiologics, surgical instruments, robotic-assisted platforms, smart implants, augmented and virtual reality guidance, three-dimensional custom implants, external fixation, non-invasive diagnostic devices and instruments, implantable devices, and surgical systems.
  • Ability to communicate effectively with others using written and verbal communication skills.
  • Interpersonal skills and the ability to work independently and within a team of technical personnel.
  • Must be a U.S. citizen or a full Green Card holder.

Responsibilities

  • Provide consultation supporting medical device reviews, including 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.
  • Provide expert consulting services to assist CDRH with its regulatory responsibilities.

Desired Qualifications

  • Familiarity with FDA medical device regulatory processes, regulations such as 21 CFR Part 878, and guidance documents.

About the Company

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