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Fda Inspector Jobs in Florida (NOW HIRING)

Inspect and approve rooms, lines and equipment prior to use by manufacturing and R&D personnel ... Monitor manufacturing areas for compliance with internal SOPs, cGMPs and FDA/DEA regulations.

Performs Quality Assurance tasks such as sampling, inspections, and tests designed to ensure manufactured products are in compliance with internal SOP's, Safety initiatives, Company policies, FDA and ...

Prepares for and helps lead responses for FDA inspections, audits, quality assurance reviews, and monitoring visits. Identifying compliance gaps and implementing processes for corrective action ...

Supports internal and external audits, FDA inspections, and regulatory compliance activities. * Assists in the development and revision of SOPs, specifications, test methods, and laboratory ...

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Fda Inspector information

See Florida salary details

$18.3K

$41.1K

$74K

How much do fda inspector jobs pay per year?

As of Jul 25, 2026, the average yearly pay for fda inspector in Florida is $41,055.00, according to ZipRecruiter salary data. Most workers in this role earn between $28,800.00 and $47,500.00 per year, depending on experience, location, and employer.

How much do FDA drug investigators make?

FDA drug investigators typically earn a salary ranging from $70,000 to $120,000 annually, depending on experience, location, and level of responsibility. They often hold a bachelor's degree in a relevant field and may require specialized training or certifications related to regulatory compliance and inspection procedures.

What types of facilities or products do FDA Inspectors typically 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.

What are the key skills and qualifications needed to thrive in the Fda Inspector position, and why are they important?

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 type of inspector gets paid the most?

Among FDA inspectors, senior or specialized inspectors, such as those overseeing complex manufacturing facilities or with advanced certifications, tend to earn higher salaries. Experience, certifications, and geographic location also influence pay levels for FDA inspectors. Generally, inspectors with specialized skills or leadership roles earn the most in this field.

Is it hard to get a job at FDA?

Becoming an FDA inspector can be competitive due to strict qualification requirements, including relevant experience, education, and passing civil service exams. Candidates often need a background in science, public health, or regulatory compliance, along with strong attention to detail and communication skills. The hiring process can be lengthy and involves multiple steps such as interviews and background checks.

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 manufacturing. They must pass a written exam and a background check, and often complete on-the-job training or specialized FDA training programs. Certification or licensing is not required but can enhance prospects.

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 are the most commonly searched types of Fda Inspector jobs in Florida? The most popular types of Fda Inspector jobs in Florida are:
What cities in Florida are hiring for Fda Inspector jobs? Cities in Florida with the most Fda Inspector job openings:
Infographic showing various Fda Inspector job openings in Florida as of July 2026, with employment types broken down into 86% Full Time, 7% Part Time, and 7% Contract. Highlights an 100% In-person job distribution, with an average salary of $41,055 per year, or $19.7 per hour.
QA Inspector

QA Inspector

ARNET PHARMACEUTICALS CORP

Fort Lauderdale, FL โ€ข On-site

Full-time

Posted 2 days ago


Job description

ESSENTIAL FUNCTIONS AND RESPONSIBILITIES:

  • Responsible for performing the inspection of in-process product, and the appropriate documentation
  • Assures cGMP compliance all at times in the production floor
  • Perform Quality Assurance tasks such as sampling, inspections, and tests designed to ensure manufactured products are in compliance with internal SOP's, Safety initiatives, Company policies, FDA and DEA regulations. Document all work performed, ensuring accuracy and thoroughness. Inform management of any deviations from established standards/procedures
  • Inspect and approve rooms, lines and equipment prior to use by manufacturing and R&D personnel
  • Approve components for in-process operations
  • Monitor manufacturing and packaging areas for compliance with internal SOPs, cGMPS and FDA/DEA regulations
  • Document all work activity in appropriate batch records, forms, and logs to ensure accuracy and compliance
  • Sample in-process items, and finished products. Perform required inspections and testing of in-process items and finished products. Process and distribute samples to different departments
  • Review records for cGMP compliance for accuracy and thoroughness and good documentation practices.
  • Inform management of problems, failures and deviations from established internal and regulatory standards
  • Apply disposition status to components and in-process materials
  • Issue QA Alerts whenever any questionable component, in-process material or product is identified at any stage of production or storage
  • Any other required duties assigned by the immediate supervisor

QUALIFICATIONS:

  • Associate degree or equivalent work experience
  • 1 - 3 yearsโ€™ experience in quality control of a manufacturing environment
  • Bilingual (English and Spanish) required
  • Knowledge in cGMP regulations and FDA guidelines
  • Detailed oriented
  • Basic computer and math skills

Monday to Friday 8:30am to 5PM