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Fda Inspector Jobs in Virginia (NOW HIRING)

Aurora Lifesciences

QC Team Lead

Manassas, VA · On-site

$90 - $120/hr

... FDA 21 CFR Part 820. Key Responsibilities * Lead and support a team of Quality Control and Receiving Inspection personnel. * Allocate daily workload, provide technical guidance, and support shift ...

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Fda Inspector information

See Virginia salary details

$24.3K

$54.5K

$98.2K

How much do fda inspector jobs pay per year?

As of Sep 4, 2026, the average yearly pay for fda inspector in Virginia is $54,468.00, according to ZipRecruiter salary data. Most workers in this role earn between $38,200.00 and $63,000.00 per year, depending on experience, location, and employer.

What does an FDA inspector do?

An FDA Inspector is responsible for ensuring that companies comply with federal regulations related to food, drugs, medical devices, and other products overseen by the U.S. Food and Drug Administration. They conduct inspections, review records, collect samples, and assess manufacturing practices to ensure public health and safety. Inspectors may also investigate complaints, issue compliance notices, and recommend enforcement actions if violations are found.

What skills and qualifications are needed to be an FDA inspector?

To thrive as an FDA Inspector, you need a solid background in science or public health, attention to detail, and thorough knowledge of regulatory standards, often supported by a relevant degree. Familiarity with inspection protocols, laboratory testing equipment, and digital reporting systems is commonly required, along with potential USDA or FDA certifications. Strong analytical thinking, effective communication, and integrity are important soft skills for this role. These competencies ensure accurate inspections, compliance with safety regulations, and clear reporting essential to public health and organizational accountability.

What types of facilities or products do FDA inspectors review, and what does a typical inspection process involve?

FDA Inspectors routinely examine a variety of facilities, such as food processing plants, pharmaceutical manufacturers, medical device companies, and cosmetic production sites, to ensure compliance with federal safety and quality regulations. A typical inspection involves reviewing operational procedures, examining production environments, sampling products, and interviewing staff to identify potential violations or risks. Inspectors often work onsite, sometimes with travel required to cover multiple locations within their region, and collaborate closely with facility management to explain findings and recommend corrective actions. This role offers the opportunity to make a significant impact on public health and provides clear advancement pathways into specialized inspection or supervisory roles within regulatory agencies.

How do you become an FDA inspector?

To become an FDA inspector, candidates typically need a bachelor's degree in a relevant field such as biology, chemistry, or food science, along with experience in food safety, pharmaceuticals, or related areas. They must pass a written exam and a background check, and often undergo specialized training at the FDA's training center. Certification or licensing is not required but can enhance prospects in the field.

What are popular job titles related to Fda Inspector jobs in Virginia?

For Fda Inspector jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Fda Inspector jobs in Virginia look for?

The top searched job categories for Fda Inspector jobs in Virginia are:

What cities in Virginia are hiring for Fda Inspector jobs?

Cities in Virginia with the most Fda Inspector job openings:

Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in Virginia as of August 2026, with employment types broken down into 92% Full Time, 4% Part Time, and 4% Contract. Highlights an 100% In-person job distribution, with an average salary of $54,468 per year, or $26.2 per hour.

FDA Program Administrator/Clinical Research Monitor

Vcu Rrtc

Richmond, VA • On-site

$70 - $80/hr

Other

Medical, Retirement

Posted 3 days ago

New

Key responsibilities

  • Develop monitoring plans for new sponsor-investigator clinical trials and studies approved through the radioactive drug research committee (RDRC).

  • Perform risk-based monitoring, author monitoring confirmation letters, follow-up reports, and assist study teams in authoring CAPAs as needed.

  • Draft and submit FDA submissions such as IND/IDE exemption, initial submissions, amendments, annual reports, safety events, closures, and emergency use requests, and assist in responding to FDA requests for information.

Job description

Advertising Summary:

Department Summary: At the VCU Office of the Vice President for Research and Innovation, our mission is to foster transformative research, discovery, and innovation at Virginia Commonwealth University through excellence in service.

We partner with faculty in all schools and departments as they seek funding, plan studies, establish collaborations, calculate budgets, submit grant applications, negotiate industry contracts, and secure patents and licensing agreements.

Our commitment to supporting and elevating the research community at VCU has resulted in record levels of sponsored research and has placed VCU among the nation’s premier public research universities.

Through our passion for discovery and willingness to take on challenges, we continue to advance the work that matters most and position the university as a national leader in research, innovation, creativity, and scholarship.

Duties & Responsibilities:

FDA program Administrator/Clinical Research Monitor

Responsibilities:

  • Perform risk-based monitoring
  • Develop monitoring plans for new sponsor-investigator clinical trials and studies that get approved through the radioactive drug research committee (RDRC)
  • Author monitoring confirmation letters and follow-up reports
  • Assist study teams in authoring CAPAs as needed
  • Maintain a dashboard to provide metrics on monitoring visits and to identify areas of risk and opportunities for training
  • Serve as a back-up for the following:
    • Draft and submit the following submissions to the FDA on behalf of the sponsor-investigators: IND/IDE exemption, IND/IDE initial submission, amendments, annual reports, safety events, closures and single patient/emergency use
    • Manage high volume of submissions at any given time with multiple urgent deadlines
    • Assist sponsor-investigator in responding to FDA’s requests for information
    • Draft and submit the following submissions to the IRB: single patient/emergency use (initial submission, reportable new information, continuing reviews, closure)
    • Maintain dashboard that provides metrics on submission time, requests for submissions and on upcoming annual reports
  • Train investigators/study teams on how to use Veeva SiteVault, eTMF and EDC and serve as a resource for questions on using the system
  • Provide best practices on how to perform aspects of clinical research
  • Assist in FDA inspections as neededOther tasks as needed

Qualifications:

Minimum Qualifications:

Demonstrated ability to work in and foster an environment of respect, professionalism and civility with a population of faculty, staff, and students from all backgrounds and experiences, or a commitment to do so as a staff member at VCU.

Only applicants who do not require current or future sponsorship for employment will be considered

  • 1-2 years of relevant work experience involving clinical research, monitoring and the FDA
  • Bachelor’s degree
  • Familiarity with the various types of FDA submissions including IND, IDEs and expanded access
  • Ability to handle high volume of studies with increasing complex study designs
  • Ability to handle high volume of FDA submissions with consistently changing deadlines
  • Experience working as a clinical research coordinator or in a role involved in clinical research
  • Ability to communicate clearly and effectively both verbally and in writing
  • Knowledge of FDA and ICH-GCP regulations
  • Ability to maintain integrity, objectivity, independence and confidentialityAbility to manage workload to work efficiently and meet deadlines as needed
  • Ability to interact with individuals of various positions and with an array of personalities
  • Experience utilizing electronic systems that are utilized in clinical research such as a CTMS, electronic investigator site file and EMR
  • Experience working with different indications
  • Have monitored clinical trials

Preferred Qualifications:

  • 3+ years of relevant work experience involving clinical research, monitoring and the FDA
  • Have monitored clinical trials
  • Experience with radiation oncology or radiopharmaceutical studies
  • Experience submitting various types of FDA submissions to the FDA for research including initial submissions, annual reports and safety reports of IND, IDEs and expanded access applications
  • Experience utilizing electronic systems that are utilized in clinical research such as a CTMS, electronic investigator site file and EMR
  • Experience working with different indications including addiction, oncology and non-oncology
  • Relevant professional certification(s) in aspects of clinical research

Salary Range:70,000 - 80,000

Benefits: All full-time university staff are eligible for VCU’s robust benefits package that includes comprehensive health benefits, paid annual and holiday leave, generous tuition benefits, retirement planning and savings options, tax-deferred annuity and cash match programs, employee discounts, well-being resources, abundant opportunities for career development and advancement, and more.

Unit: Office of the Vice President for Research & Innovation

Department: Strategy and Regulatory Affairs

FLSA Exemption Status: Exempt

Hours per Week: 40

Restricted Position: Yes

ORP Eligible: No

Flexible Work Arrangement: Hybrid

University Job Title: 25234N - Sr Specialist LG 1 - Open

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