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Fda Inspector Jobs in Jacksonville, FL (NOW HIRING)

Treace

Quality Engineer

Ponte Vedra, FL

$65K - $84K/yr

Responsible for creating and maintaining process risk management files to meet FDA and ISO standards * Reviews product and documentation non-conformances and recommends inspection, product and/or ...

New

Treace

Quality Engineer

Ponte Vedra, FL · On-site

$65K - $84K/yr

Responsible for creating and maintaining process risk management files to meet FDA and ISO standards * Reviews product and documentation non-conformances and recommends inspection, product and/or ...

New

Vhr_unither

QA Specialist II - EVLP

Jacksonville, FL · Hybrid

... FDA and other regulatory inspections by supporting the timely and accurate transfer of data, documents, and information to inspectors while exercising discretion * Maintain quality files, both ...

nexAir

Route Driver

Jacksonville, FL · On-site

$17.25 - $22.25/hr

... trip inspections per DOT regulations. • Complete all FDA/DOT required documentation. • Track delivery and pick-up of cylinders at customer sites using handheld device and complete all the ...

nexAir

Route Driver

Jacksonville, FL · On-site

$17.25 - $22.25/hr

Perform all required pre- and post-trip inspections per DOT regulations. * Complete all FDA/DOT required documentation. * Track delivery and pick-up of cylinders at customer sites using handheld ...

Planet 13

Quality Control Specialist

Jacksonville, FL · On-site

$18/hr

FDA, HACCP, SQF experience * Prior experience in Quality Assurance or Quality Control function * Prior experience with product sampling, inspection procedures, customer complaints, product ...

Planet 13

Quality Control Specialist

Jacksonville, FL · On-site

$18/hr

FDA, HACCP, SQF experience * Prior experience in Quality Assurance or Quality Control function * Prior experience with product sampling, inspection procedures, customer complaints, product ...

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All JobsFda Inspector JobsFda Inspector Jobs in Jacksonville, FL

Fda Inspector information

See Jacksonville, FL salary details

$21.8K

$49K

$88.2K

How much do fda inspector jobs pay per year?

As of Aug 15, 2026, the average yearly pay for fda inspector in Jacksonville, FL is $48,957.00, according to ZipRecruiter salary data. Most workers in this role earn between $34,300.00 and $56,600.00 per year, depending on experience, location, and employer.

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.

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.

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 the FDA's specialized training program and often require a background check and security clearance; some positions may also require state licensure or certifications. Strong attention to detail, knowledge of regulatory standards, and good communication skills are essential for the role.

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 popular job titles related to Fda Inspector jobs in Jacksonville, FL?

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

What job categories do people searching Fda Inspector jobs in Jacksonville, FL look for?

The top searched job categories for Fda Inspector jobs in Jacksonville, FL are:

What cities near Jacksonville, FL are hiring for Fda Inspector jobs?

Cities near Jacksonville, FL with the most Fda Inspector job openings:

Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in Jacksonville, FL as of August 2026, with employment types broken down into 75% Full Time, 12% Part Time, 12% Contract, and 1% Nights. Highlights an 97% Physical, and 3% Remote job distribution, with an average salary of $47,822 per year, or $23 per hour.

Quality Engineer

Treace

Ponte Vedra, FL

$65K - $84K/yr

Full-time

Posted 2 days ago

New

Job description

Company Description

Treace's mission is to be the leader in the surgical treatment of bunions by establishing the Lapiplasty System as the standard of care. We are committed to operating our business with the highest standards of ethical conduct. We intend to exceed our customers' expectations through an innovation-driven, high-velocity approach to solving treatment and surgical problems. With our products and services, our mission is to assist foot and ankle surgeons in improving patient outcomes and reducing healthcare costs, while providing rewarding experiences and opportunities for our employees and stakeholders.

Job Description

POSITION SUMMARY:

The Quality Engineer (QE) will be responsible for management and execution of assigned quality projects in order to meet quality assurance objectives. The QE shall have prior experience working within an FDA compliant Title 21 section 820 environment and the ability to work cross-functionally to support rapid growth and continuous improvement. This position primarily will support in-house manufacturing operations.

PRIMARY DUTIES AND RESPONSIBILITIES:

  • Creates and updates quality system procedures working on cross-functional teams to align best practices, procedures, and applicable regulations (FDA, ISO, etc.)
  • Evaluates product changes and directs appropriate disposition of product through the company's change control system
  • Assemble non-sterile product into kits for final release into the field
  • Participate in setup, qualification, calibration, and maintenance of manufacturing and inspection equipment
  • Responsible for creation of inspection models, inspection prints, gaging, or other inspection documents and detailed testing requirements to insure receipt of quality product
  • Support concurrent engineering efforts by participating in design development projects representing quality assurance and the customer (supplier and end user)
  • Responsible for creating and maintaining process risk management files to meet FDA and ISO standards
  • Reviews product and documentation non-conformances and recommends inspection, product and/or quality system modifications
  • Interfaces with supplier quality representatives concerning issues with quality assurance and assures that effective corrective action is implemented
  • Assists in inspection of work-in-progress, finished parts and assemblies, kits and completion of associated paperwork for final release of product
  • Assists in reviewing patient-specific instrumentation designs
  • Participates in projects and help drive and build a Continuous Improvement and Lean culture across the organization
Qualifications

MINIMUM REQUIREMENTS:

Education and Experience: Bachelor's degree in Engineering, Science, Technology or a related discipline with 3+ years of progressive medical device engineering experience (Manufacturing, Development or Quality Engineering) within an FDA compliant Title 21 section 820 environment

Additional Information

All your information will be kept confidential according to EEO guidelines.

Treace's Privacy Policy

It is Treace's policy not to discriminate against any applicant for employment, or any employee because of age, color, sex, disability, national origin, race, religion, veteran status or any other characteristic protected by applicable law. EEO/Disabled/Veterans Employer
 

Treace is a drug free employer.

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