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Fda Inspector Jobs in Miami, FL (NOW HIRING)

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

Careerxchange

Operations Manager Clinical Trials

Miami, FL · On-site

$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 ...

5TH HQ LLC

Production Supervisor

Plantation, FL · On-site

$19 - $20/hr

Conduct regular inspections of equipment and workstations to ensure a safe and efficient work ... Strong understanding of GMP standards and FDA regulations. Proven leadership and team management ...

5TH HQ LLC

Production Supervisor

Plantation, FL · On-site

$19 - $20/hr

Conduct regular inspections of equipment and workstations to ensure a safe and efficient work ... Strong understanding of GMP standards and FDA regulations. Proven leadership and team management ...

W3Global Inc.

Food Quality Assurance Specialist

Hialeah, FL · On-site

$40K - $50K/yr

FDA/USDA Holds: Review release notices, update system status, and manage detained or rejected shipments to expedite resolution. * Receiving Program: Collect and inspect batch samples, complete QC and ...

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All JobsFda Inspector JobsFda Inspector Jobs in Miami, FL

Fda Inspector information

See Miami, FL salary details

$23.4K

$52.5K

$94.7K

How much do fda inspector jobs pay per year?

As of Sep 5, 2026, the average yearly pay for fda inspector in Miami, FL is $52,546.00, according to ZipRecruiter salary data. Most workers in this role earn between $36,800.00 and $60,700.00 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 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
Infographic showing various Fda Inspector job openings in Miami, FL as of August 2026, with employment types broken down into 91% Full Time, 6% Part Time, 2% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $52,546 per year, or $25.3 per hour.

Bilingual Quality Assurance Document Control

5TH HQ LLC

Fort Lauderdale, FL

$19/hr

Full-time

Re-posted 23 days ago

Job description

Quality Assurance (QA) Document Control Specialist

A well-established pharmaceutical company in Miramar, FL is seeking an experienced and detail-oriented Quality Assurance (QA) Document Control Specialist to support its evening shift operations. This role is responsible for maintaining, reviewing, and managing GMP documentation to ensure compliance with regulatory standards. The ideal candidate is bilingual (English/Spanish), organized, and has prior experience in pharmaceutical or FDA-regulated environments.

Location: Miramar, FL Industry: Pharmaceutical Manufacturing Job Type: Full-Time Schedule: Monday to Friday, 2:30 PM – 11:00 PM Pay: $19.00 per hour

Key Responsibilities

  • Maintain and control quality documentation in accordance with GMP and FDA guidelines
  • Review and archive manufacturing, packaging, and testing records for accuracy and completeness
  • Ensure proper version control and distribution of controlled documents (SOPs, batch records, etc.)
  • Assist in audits, inspections, and internal reviews by preparing and providing requested documentation
  • Support QA team in implementing document changes, updates, and approvals
  • Ensure timely and accurate entry of documentation into digital or physical filing systems
  • Collaborate with production, quality, and regulatory departments to ensure documentation compliance
  • Report any deviations or non-conformances found in records

Qualifications

  • Minimum 1–2 years of experience in document control or QA in a pharmaceutical or FDA-regulated environment
  • High school diploma or equivalent required; associate or bachelor's degree preferred
  • Strong knowledge of GMP, SOPs, and document control best practices
  • Excellent attention to detail and organizational skills
  • Bilingual (English/Spanish) – required
  • Proficient in Microsoft Office (Excel, Word, Outlook)
  • Ability to work independently with minimal supervision during evening shift hours
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