1

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

Manufacturing Manager

Fort Lauderdale, FL ยท On-site

$118K - $196K/yr

Direct preparation for and execution of internal, customer, corporate, and regulatory audits, including FDA inspections. * Investigate product quality issues and implement corrective actions in ...

Direct preparation for and execution of internal, customer, corporate, and regulatory audits, including FDA inspections. * Investigate product quality issues and implement corrective actions in ...

Lead FDA, customer, and third-party audits and inspections, acting as the primary quality representative and ensuring effective communication and responses. * Coordinate inspection preparation ...

New

QA MANAGER

Boca Raton, FL ยท On-site

$95K - $110K/yr

Participate in internal, customer, and regulatory inspections, including FDA and other regulatory agency audits, and assist in preparing responses to audit observations. * Develop, revise, review ...

New

next page

Showing results 1-20

Fda Inspector information

See Delray Beach, FL salary details

$23K

$51.6K

$93K

How much do fda inspector jobs pay per year?

As of Jul 30, 2026, the average yearly pay for fda inspector in Delray Beach, FL is $51,588.00, according to ZipRecruiter salary data. Most workers in this role earn between $36,200.00 and $59,600.00 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 cities near Delray Beach, FL are hiring for Fda Inspector jobs? Cities near Delray Beach, FL with the most Fda Inspector job openings:
Infographic showing various Fda Inspector job openings in Delray Beach, FL as of July 2026, with employment types broken down into 82% Full Time, 14% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $51,588 per year, or $24.8 per hour.

QA Inspector Bilingual EnglishSpanish

5TH HQ

Fort Lauderdale, FL โ€ข On-site

Full-time

Posted 15 days ago


Job description

We're currently seeking a bilingual QA Inspector for one of our clients in Davie, FL. This is an excellent opportunity for a detail-oriented quality professional with experience in a cGMP manufacturing environment who is looking to join a growing organization committed to quality, safety, and regulatory compliance. Location: Davie, FL Schedule: Mondayโ€“Friday, 5:30 AM โ€“ 2:00 PM (1st Shift) Employment Type: Full-Time, Temp-to-Hire ESSENTIAL FUNCTIONS AND RESPONSIBILITIES Responsible for performing inspections of in-process products and completing the appropriate documentation. Ensure cGMP compliance at all times on the production floor. Perform Quality Assurance tasks such as sampling, inspections, and testing to ensure manufactured products comply with internal SOPs, safety initiatives, company policies, and FDA and DEA regulations. Document all work performed, ensuring accuracy and completeness. Inform management of any deviations from established standards or procedures. Inspect and approve rooms, production 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, cGMP regulations, and FDA/DEA requirements. Document all work activities in batch records, forms, and logs to ensure accuracy and compliance. Sample in-process materials and finished products. Perform required inspections and testing, then process and distribute samples to the appropriate departments. Review records for cGMP compliance, accuracy, completeness, and Good Documentation Practices (GDP). Inform management of problems, failures, and deviations from internal and regulatory standards. Apply disposition status to components and in-process materials. Issue QA Alerts whenever questionable components, in-process materials, or finished products are identified during production or storage. Perform other duties as assigned by the immediate supervisor. QUALIFICATIONS Associate degree or equivalent work experience. 1โ€“3 years of Quality Assurance or Quality Control experience in a manufacturing environment. Previous warehouse experience preferred. Experience operating a manual or electric pallet jack preferred. Bilingual (English/Spanish) required. Knowledge of cGMP regulations and FDA guidelines. Detail-oriented. Basic computer and math skills. PHYSICAL REQUIREMENTS Requires standing, walking, bending, lifting, and handling chemicals, as well as using computers and monitoring equipment. Must be able to lift and carry boxes weighing up to 50 pounds on a regular basis. Must be able to wear appropriate PPE, including face masks, respirators, safety goggles, and hearing protection. TYPICAL WORK CONDITIONS Subject to exposure to food and nutritional bulk ingredients that may affect the respiratory system or skin, including odors, dust, and airborne allergens. Works in a dry, low-moisture manufacturing environment with exposure to normal workplace hazards, including proximity to moving mechanical parts and moderate industrial noise. #J-18808-Ljbffr


5th HQ logo

About 5th HQ

Sourced by ZipRecruiter

We are a boutique Staffing & Recruiting agency that provides a full range of employment solutions that include full-time, temporary, and part-time employment in a wide range of positions, including Professional, Light Industrial, and Office Services.

Industry

Recruiting and staffing services

Headquarters location

Plantation, FL, US