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Fda Public Health Jobs (NOW HIRING)

Accompany an FDA-commissioned inspector to designated retail locations to assess compliance with ... Contribute to public health and safety by ensuring compliance with tobacco control laws. * Work as ...

Accompany an FDA-commissioned inspector to designated retail locations to assess compliance with ... Contribute to public health and safety by ensuring compliance with tobacco control laws. * Work as ...

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Phoenix, AZ · On-site

$52K/yr

Knowledge of: • Public health principles, environmental health, regulatory inspection procedures ... Department of Health and Human Services, Food and Drug Administration (FDA), under the authority of ...

Alston & Bird is seeking an experienced FDA consultant to work with the Health Care team's FDA ... Ability to travel to private and public buildings, domestically and internationally, via private or ...

Alston & Bird is seeking an experienced FDA consultant to work with the Health Care team's FDA ... Ability to travel to private and public buildings, domestically and internationally, via private or ...

Showing results 21-40

Fda Public Health information

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$37K

$79.7K

$127.5K

How much do fda public health jobs pay per year?

As of Aug 12, 2026, the average yearly pay for fda public health in the United States is $79,657.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $89,000.00 per year, depending on experience, location, and employer.

What are the typical daily responsibilities of an FDA Public Health professional?

As an FDA Public Health professional, your daily activities may include reviewing and analyzing public health data, drafting and enforcing regulatory recommendations, and collaborating with other federal and state agencies to safeguard public safety. You might also participate in the evaluation of food, drug, and medical device safety, conduct site inspections, and prepare reports on findings. The role often involves multidisciplinary teamwork and ongoing communication with industry stakeholders, which helps ensure that public health standards are met and maintained. Over time, you may engage in projects that contribute to policy development and national health initiatives.

What are the key skills and qualifications needed to thrive in the FDA Public Health position?

To thrive as an FDA Public Health professional, you need a solid background in public health, epidemiology, regulatory compliance, and typically a degree in public health or a related field. Familiarity with data analysis software, federal regulatory systems, and certifications such as Certified in Public Health (CPH) are commonly expected. Strong analytical thinking, problem-solving, and effective communication are critical soft skills for this role. These abilities are essential to ensure effective oversight, compliance with FDA regulations, and impactful public health outcomes.

What is an FDA Public Health?

An FDA Public Health job involves working to protect public health by ensuring the safety, efficacy, and security of food, drugs, medical devices, and other regulated products. Professionals in this role conduct research, develop policies, inspect facilities, and analyze data to identify potential health risks. They work across various specialties such as epidemiology, toxicology, and regulatory affairs to uphold public safety and compliance with FDA regulations.

More about Fda Public Health jobs
What cities are hiring for Fda Public Health jobs? Cities with the most Fda Public Health job openings:
What states have the most Fda Public Health jobs? States with the most job openings for Fda Public Health jobs include:
Infographic showing various Fda Public Health job openings in the United States as of August 2026, with employment types broken down into 50% Full Time, and 50% Part Time. Highlights an 100% In-person job distribution, with an average salary of $79,657 per year, or $38.3 per hour.

Full-time

Re-posted 14 hours ago


Job description

FDA CDRH - Medical Officer (Surgical Oncologist) SME Position Description 

The mission of the FDA Center for Devices and Radiological Health (CDRH) is to protect and promote the public health. CDRH assures that patients and providers have timely and continued access to safe, effective, and high-quality medical devices and safe radiation-emitting products.

Tunnell Government Services, Inc. is providing professional and scientific services to the CDRH with expert consultants with scientific expertise in the regulation and approval and of medical devices. In general, these consultants provide consultation related to supporting medical device reviews (EUA, 510(k), PME and De Novo marketing applications, Pre-submissions); participate in meetings and teleconferences; coordinate meetings with internal and external stakeholders; develop written reviews and correspondence; perform research; conduct data analysis; write detailed documents and reports; and execute other administrative office tasks related to CDRH's projects.

Tunnell is seeking a candidate to provide expert consulting services to assist the CDRH with their regulatory responsibilities. This candidate should possess specific expertise and training in surgical oncology, as relevant to medical devices.

Requirements and Qualifications

  • The candidate must possess a Doctor of Medicine (M.D. or equivalent) from an accredited medical school in the United States.
  • In addition, 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 (10) years of relevant clinical experience
  • Certification from a U.S. relevant specialty board organization, e.g., the American Board of Surgery (ABS), Society of Surgical Oncology (SSO), etc.  
  • Thorough understanding of current clinical practices in surgical oncology, including diagnosis and treatment, and current/emerging trends in practice.
  • Expert in function and utilization of medical devices commonly used as part of surgical oncology (e.g., advanced energy and resection devices [electrosurgical units, ultrasonic scalpels, argon beam coagulators], minimally invasive and robotic platforms [robotic-assisted surgery systems, laparoscopes and thoracoscopes], localization and navigation devices [tumor localization seeds, intraoperative ultrasound], tumor ablation systems [radiofrequency ablation and microwave ablation, cryoablation systems, irreversible electroporation], lymph node mapping systems [gamma probes, near-infrared fluorescence imaging], intraoperative therapy devices [hyperthermic intraperitoneal chemotherapy pumps, intraoperative radiation therapy systems]).
  • Familiarity with relevant FDA medical device regulatory processes, regulations (e.g., 21 CFR Part 878 - General and Plastic Surgery Devices), and guidances is preferred.
  • Ability to communicate well with others using excellent written and verbal communication skills.
  • Excellent interpersonal skills, with the ability to effectively work both independently and within a team of technical personnel.

This position is 100% telework. 

Must be a US Citizen or a Full Green Card holder.