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Fda Inspector Jobs in Daytona Beach, FL (NOW HIRING)

InSpec Solutions LLC

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Quality Manager

Holly Hill, FL · On-site

$50K - $80K/yr

Maintain and renew key certifications and regulatory requirements (cGMP, FDA registration, ISO ... Oversee product quality systems: incoming inspection, in-process checks, finished goods release ...

Express Employment Professionals

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Manufacturing Set up Technician - 3rd Shift

Deland, FL · On-site

$18 - $19/hr

The primary purpose of this position is to set-up, maintain, operate, test and inspect product, and perform repairs on associated departmental equipment in conformance to FDA, GMP's, ISO 13485 ...

Actalent

Analytical Lab Technician

Ormond Beach, FL · On-site

Support preparation for regulatory inspections and FDA audits by maintaining documentation and laboratory practices in an audit-ready state. * Perform additional tasks assigned by the QC Supervisor ...

Actalent

Analytical Lab Technician

Ormond Beach, FL · On-site

Support preparation for regulatory inspections and FDA audits by maintaining documentation and laboratory practices in an audit-ready state. * Perform additional tasks assigned by the QC Supervisor ...

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Fda Inspector information

See Daytona Beach, FL salary details

$23.5K

$52.7K

$95K

How much do fda inspector jobs pay per year?

As of Sep 6, 2026, the average yearly pay for fda inspector in Daytona Beach, FL is $52,743.00, according to ZipRecruiter salary data. Most workers in this role earn between $37,000.00 and $61,000.00 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 cities near Daytona Beach, FL are hiring for Fda Inspector jobs?

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

Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in Daytona Beach, FL as of August 2026, with employment types broken down into 83% Full Time, 14% Part Time, 2% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $52,743 per year, or $25.4 per hour.

Quality Manager

InSpec Solutions LLC

Holly Hill, FL • On-site

$50K - $80K/yr

Full-time

Medical, Dental, Vision, Life, PTO

Re-posted 5 days ago

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Job description

The Quality Manager will execute a comprehensive quality system, manage a growing quality team, and ensure compliance across all product categories. This role is highly hands-on and essential to maintaining regulatory readiness, with expected growth ahead.


Key Responsibilities:

  • Build and oversee a quality team, including staffing, training, and ongoing development.
  • Execute, and continue to develop, implement, and update SOPs across manufacturing, testing, and documentation workflows for medical devices, OTC products, and cosmetics.
  • Maintain and renew key certifications and regulatory requirements (cGMP, FDA registration, ISO 13485, OTC monograph compliance, cosmetic GMP).
  • Lead audit preparation, on-site audits, and follow-up activities.
  • Design and execute document control processes, including electronic batch records, deviations, CAPAs, and change management.
  • Oversee product quality systems: incoming inspection, in-process checks, finished goods release, stability studies, and complaint handling.
  • Partner with production, R&D, and commercial teams to embed quality throughout the product lifecycle.
  • Track and improve quality metrics such as defect rates, audit findings, and out-of-specification events.
  • Ensure all activities align with FDA, industry standards, and applicable international regulations.


Qualifications

  • 5+ years of quality assurance or quality management experience in contract manufacturing, ideally with exposure to medical devices, OTC products, or cosmetics.
  • Experience building quality systems and teams, especially in a scale-up or startup environment.
  • Strong knowledge of regulatory standards including 21 CFR Part 210/211, cGMP, and cosmetic regulations.
  • Hands-on experience writing SOPs, implementing QMS processes, and managing document control.
  • Excellent project management and multitasking capabilities.
  • Effective communicator able to train teams and interact confidently with auditors.
  • Bachelor's degree in a relevant scientific or engineering discipline preferred; ASQ certifications are a plus.
  • Detail-oriented, proactive, and adaptable in a dynamic environment.


This role offers a competitive salary, with a great compensation package, and strong opportunities for growth.

Company Description

InSpec Solutions, LLC is a market leading contract manufacture of topical OTC and Cosmetic Products. We are experience rapid growth and can offer boundless opportunities for growth.