Deputy Director, Chief Medical Officer, Office of Product Evaluation and Quality

Food and Drug Administration · White Oak, MD

Full-time$235,000 – $340,795 per year
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Department of Health and Human Services

This position is being filled under a stream-lined hiring authority, Title 21 of the United States Code (21 US Code 379d-3a) as amended by the 21st Century Cures Act of 2016, section 3072 and the Consolidated Appropriations Act of 2023, Section 3624. The candidate selected for this position will serve under a career or career-conditional appointment and be paid under the provisions of this authority. This position is being recruited based on the Title 21 Pay Table 6, Band G .

  • Serves as Deputy Director and Chief Medical Officer for OPEQ, providing executive leadership and strategic direction for FDA medical device programs.
  • Serves as OPEQ's senior clinical authority, providing expert guidance on complex clinical, scientific, regulatory, and public health issues.
  • Oversees premarket and postmarket medical device review, including 510(k)s, PMAs, De Novo requests, IDEs, and postmarket surveillance.
  • Leads clinical oversight of regulatory decisions affecting the safety, effectiveness, quality, and performance of medical devices.
  • Provides benefit-risk expertise for premarket and postmarket regulatory decision-making involving medical devices.

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Listed under Healthcare & Nursing jobs.

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