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Fda Inspector Jobs in Miami, FL (NOW HIRING)

JRG Partners

QC/Sanitation Supervisor

Doral, FL · On-site

Ensure compliance with FDA, USDA, HACCP, GMP, SOP, and SSOP requirements. * Conduct plant, pre-operational, raw material, and internal inspections. * Train employees on sanitation procedures, GMPs ...

Careerxchange

Quality Control Specialist/Vendors

Hialeah, FL · On-site

$45K - $55K/yr

Review and manage FDA/USDA holds, releases, and compliance issues * Perform receiving inspections, including sampling and QC reporting * Evaluate vendor samples and ensure adherence to quality ...

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Aerotek

Assembler

Miami, FL · On-site

$17.25 - $21/hr

You will perform intricate builds, conduct detailed quality inspections, and strictly follow FDA and ISO medical device regulations to ensure every product meets exacting clinical standards.

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Spices Usa Inc

Quality Control Manager

Hialeah, FL · On-site

$60K - $80K/yr

Strong knowledge of FSVP, GMPs, SQF, and FDA regulations * SAP proficiency and strong organizational skills * Bilingual communication (English/Spanish) * Experience managing audits or inspections

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Careerxchange

Operations Manager Clinical Trials

Miami, FL

$41 - $56/hr

Ensure compliance with FDA regulations, Good Clinical Practice (GCP), IRB requirements, and sponsor ... Prepare for sponsor visits, monitoring visits, audits, and regulatory inspections. * Identify ...

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5TH HQ

Quality Assurance Technician

Hollywood, FL

Estamos buscando un Inspector de Aseguramiento de Calidad en Miramar, FL, quien será responsable ... FDA y DEA, documentando todo el trabajo realizado, asegurando precisión y exhaustividad, e ...

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All JobsFda Inspector JobsFda Inspector Jobs in Miami, FL

Fda Inspector information

See Miami, FL salary details

$22.2K

$49.8K

$89.7K

How much do fda inspector jobs pay per year?

As of Jul 1, 2026, the average yearly pay for fda inspector in Miami, FL is $49,781.00, according to ZipRecruiter salary data. Most workers in this role earn between $34,900.00 and $57,500.00 per year, depending on experience, location, and employer.

What type of inspectors make the most money?

Within the FDA inspection roles, senior-level inspectors such as Supervisory Food and Drug Inspectors or those with specialized expertise in areas like pharmaceuticals or biotechnology tend to earn higher salaries. Factors influencing pay include experience, certifications, and the complexity of inspections conducted, often requiring advanced knowledge of regulations and compliance standards.

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 are the four types of FDA Inspections?

FDA inspectors conduct four main types of inspections: routine inspections to monitor compliance, for-cause inspections triggered by specific concerns or complaints, follow-up inspections to verify corrective actions, and pre-approval inspections for new drug or device applications. These inspections help ensure that facilities meet regulatory standards for safety and quality.

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 fields, along with strong attention to detail and knowledge of FDA regulations. 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 training at the FDA's training center. 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 Miami, FL? For Fda Inspector jobs in Miami, FL, the most frequently searched job titles are:
What job categories do people searching Fda Inspector jobs in Miami, FL look for? The top searched job categories for Fda Inspector jobs in Miami, FL are:
What cities near Miami, FL are hiring for Fda Inspector jobs? Cities near Miami, FL with the most Fda Inspector job openings:
Fda Inspector jobs near you

Quality Assurance Coordinator (Clinical Research)

Research Centers of America

Hollywood, FL

$22.25 - $29.50/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 7 days ago

Job description

About Us:

Each of CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.

Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.

Job Summary:

Ensure that highest standards of data quality and study participant safety are maintained, as well as adherence to study protocols, CenExel SOPs, Site Working Practices (WPs), ICH GCP, Code of Federal Regulations, and IRB Guidelines.

Essential Responsibilities and Duties:

  • Assists the QA Manager in the development, implementation and follow-up of quality assurance programs including necessary or appropriate policies and guidelines.
  • Reviews follow-up monitoring visit reports, protocol deviation logs, and quality findings trackers for trend analysis.
  • Performs ongoing review of a percentage sampling of study inclusion/exclusion, study procedure records, and laboratory reports to ensure that they are conducted according to the protocol, applicable SOPs, ICH/GCP guidelines and federal regulations.
  • Performs quality review of initially created source documentation, including amendments, to ensure all protocol required procedures are present.
  • Prepares for internal and external audits and FDA inspections.
  • Attends staff meetings.
  • Attends site initiation visits as needed.
  • Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies.
  • Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Education/Experience/Skills:

  • Must be able to effectively communicate verbally and in writing in English and Spanish.
  • High school graduate or equivalent, Bachelors degree or equivalent preferred.
  • Minimum 1-2 years relevant experience in the clinical research industry.
  • Knowledge/Skills/Abilities: Must be self-directed and able to work with minimal supervision; Must have in depth knowledge of FDA regulations. GCP, and ICH guidelines; Able to take a flexible approach to shifting priorities; Able to manage multiple projects and responsibilities; Motivated to work consistently in a fast paced and rapidly changing environment; Must be detail oriented and have exceptional computer, organizational, and communication skills – both written and oral.
  • Must reflect the professional image of the company, upholding the company vision in actions, demeanor, and appearance.
  • Must be able to clearly communicate through written and verbal means with sponsors and staff.

 

Working Conditions

  1. Indoor, Office environment.
  2. Essential physical requirements include sitting, typing, standing, walking.
  3. Lightly active position, occasional lifting of up to 20 pounds.
  4. Reporting to work, as scheduled, is essential.
  5. On-site work arrangement.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.

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