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Fda Inspector Jobs in Virginia (NOW HIRING)

Granules

Quality Assurance Manager

Manassas, VA · On-site

The person will be responsible for managing and ensuring that facility meets all GMP, FDA and SOP requirements. * Managing all quality operations to include inspection of components, bulk, and final ...

Vhr_unither

QA/QC Manager - DPF

Christiansburg, VA · On-site

... FDA or other regulatory inspections; interpret inspection direction and respond quickly to mitigate potential issues; support timely and accurate data/document transfer to inspectors; act with ...

Socket.dev

Production Engineer

Chantilly, VA · On-site

$85 - $105/hr

Knowledge of FDA regulations, cGMP requirements, and manufacturing compliance standards. * Understanding of manufacturing line operations, serialization, labeling, coding, and inspection systems.

Granules

Production Engineer

Chantilly, VA · On-site

$60K - $75K/yr

Knowledge of FDA regulations, cGMP requirements, and manufacturing compliance standards. * Understanding of manufacturing line operations, serialization, labeling, coding, and inspection systems.

Spectrum Brands

Quality Technician II

Blacksburg, VA · On-site

$15.75 - $21.25/hr

Inspect raw materials, in-process products, and finished goods to ensure compliance with quality ... Experience working in a regulated environment, preferably FDA-regulated manufacturing.

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All JobsFda Inspector JobsFda Inspector Jobs in Virginia

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.

Quality Assurance Manager

Granules

Manassas, VA • On-site

Full-time

Re-posted 14 days ago

Key responsibilities

  • Manage and ensure that the facility meets all GMP, FDA, and SOP requirements.

  • Lead the communication of open quality document notifications and resolution between departments regarding complaints, investigations, change control, CAPAs, and other quality documents.

  • Perform documentation for all quality system functions in accordance with cGMP, SOPs, and applicable laws.

Job description

Description:

*This is an Onsite Role**


The QA Manager ensures compliance with cGMP and internal policies, procedures and specifications. This position is responsible for performing documentation for all quality system functions in accordance with cGMP and related company SOP’s, state, federal and local laws as applicable. This person should be knowledgeable of cGMP requirements, FDA regulations and ICH guidelines.

  • The person will be responsible for managing and ensuring that facility meets all GMP, FDA and SOP requirements.
  • Managing all quality operations to include inspection of components, bulk, and final products for the Manassas, VA, ensuring release lead times are met with timely product disposition.
  • Ensure that the facility is meeting all training requirements.
  • Lead the communication of open quality document notification and resolution between all departments regarding Complaints, Investigations, Change Control, CAPA’s (including verification of CAPA’s) and other quality documents as needed.
  • Manage and maintain audit inspections (Internal and External) for the site.
  • Responsible for supporting the preparation, review, processing, and approval of various validation documents as application for the Granules, Manassas, facility.
  • Provide QA support, review and approval for relevant documents including relevant procedures, batch records, specifications, stability reports, technical reports (i.e., Qualification, Validation, Transportation.), trend reports, Annual Product Quality Reviews and other documents as needed.
  • Responsible for performance and development of all Quality Assurance staff through mentoring and focusing on personal and professional growth.
  • Work with Quality leadership team for proactive succession planning and a high-performance culture through people.
  • Guide and lead by setting realistic personal goals for staff and provide regularly scheduled feedback throughout the year.
  • Provide the means for incorporating the necessary tools, equipment, and methods into the new and existing processes aimed at continuous improvement.
  • Implementation Quality management system tools and their compliance.
  • Development and execution of quality training modules for the organization.
  • Ensure staff receives appropriate knowledge and skill development and growth opportunities
  • Work with Regulatory Affairs to supply information needed for FDA filings.
  • Other duties as assigned by management.

 


Requirements:

Knowledge & Skills


· Expert-level knowledge of the FDA guidance for Industry, Title 21 of the Code of Federal Regulations and Compendia (USP/EP/BP/etc...)

· cGMP compliance within the pharmaceutical manufacturing industry.

· Writing and maintaining cGMP documentation.

· Analyze data/information and resolve complex issues.

· Verbal and written communication skills.

· Work and communicate with cross-functional teams.

· Multiple priorities and re-prioritize tasks.

· Strong computer skills and working knowledge of Microsoft Office Suite and Adobe

· Demonstrated ability to work on complex assignments in collaboration with various departments.


Experience & Education


· Bachelor's degree in the life sciences (or equivalent work experience) minimum of 6+ years in a QA role within the pharmaceutical industry

· Master’s degree with 4+ years of pharmaceutical manufacturing experience and at least 3 years of those years in a progressive challenging QA department in the pharmaceutical industry.


Physical Requirements/Working Environment


· While performing the duties of this job, the employee is regularly required to, stand, sit, talk, hear, and use hands and fingers to operate a computer and telephone keyboard.

· Specific vision abilities required by this job include close vision requirements due to computer work.

· Ability to sit at a computer terminal for an extended period of time.

· Light to moderate lifting up to 10-15 lbs is required.

· Ability to work in a confined area