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Fda Jobs in Miami, FL (NOW HIRING)

5th HQ

Regulatory Support Specialist

Miramar, FL

$17 - $19/hr

This role is responsible for ensuring compliance with FDA regulations and maintaining regulatory documentation related to manufacturing, packaging, labeling, and holding operations for dietary ...

5th HQ

Bilingual Manufacturing Coordinator

Miramar, FL · On-site

$20 - $22/hr

The ideal candidate will coordinate daily production activities, ensure compliance with FDA and GMP regulations, and support overall production efficiency and quality. Key Responsibilities:

5th HQ

Manufacturing Coordinator

Pembroke Pines, FL

$22 - $25/hr

The ideal candidate will coordinate daily production activities, ensure compliance with FDA and GMP regulations, and support overall production efficiency and quality. Key Responsibilities:

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 ...

Hephaestus Pharmacy

Certified Pharmacy Technician

Doral, FL

$16.75 - $20.25/hr

Position Overview The Certified Pharmacy Technician supports pharmacy operations by receiving, storing, picking, packing, and shipping pharmaceutical products in compliance with FDA, USP, DEA (if ...

Spices Usa Inc

Quality Control Manager

Hialeah, FL · On-site

Maintain active certifications including Kosher, Organic, USDA, FDA, COA, and Phytosanitary * Coordinate renewal processes and ensure documentation remains current and accessible Meetings ...

5TH HQ LLC

Manufacturing Supervisor

Plantation, FL · On-site

$25 - $28/hr

Ensure compliance with FDA regulations and GMP standards. * Implement and monitor quality control procedures. * Drive continuous improvement initiatives to increase efficiency and reduce waste.

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How much do fda jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for fda in Miami, FL is $36.66, according to ZipRecruiter salary data. Most workers in this role earn between $22.84 and $45.68 per hour, depending on experience, location, and employer.

What does an FDA professional do?

An FDA professional works for the U.S. Food and Drug Administration, a federal agency responsible for protecting public health by ensuring the safety and efficacy of drugs, medical devices, food, cosmetics, and other products. Their roles can include reviewing and approving new drugs and medical devices, conducting inspections, enforcing regulations, and providing guidance to industries. FDA professionals may also work in research, policy development, and public outreach to ensure that products meet regulatory standards and are safe for consumer use.

What are the key skills and qualifications needed to thrive as an FDA Regulatory Affairs Specialist, and why are they important?

To thrive as an FDA Regulatory Affairs Specialist, you need a strong background in life sciences, regulatory guidelines, and compliance, usually supported by a relevant degree such as pharmacy, biology, or chemistry. Familiarity with regulatory submission systems, FDA regulations (such as 21 CFR), and certifications like RAC (Regulatory Affairs Certification) are highly beneficial. Attention to detail, strong analytical thinking, and effective communication skills help professionals navigate complex regulations and collaborate with cross-functional teams. These competencies ensure that products meet legal requirements and safety standards, facilitating successful approvals and market access.

What are some typical challenges faced by professionals working at the FDA, and how can they be managed?

Professionals at the FDA often navigate complex regulatory requirements, tight deadlines, and the need to balance public health priorities with industry innovation. Collaborating across multidisciplinary teams and staying updated on evolving scientific data are essential parts of the role. Adapting to frequent changes in policy and handling high volumes of submissions can be demanding, but leveraging strong communication skills and seeking mentorship within the agency can help manage these challenges effectively.

What is the difference between Fda vs Food Scientist?

AspectFdaFood Scientist
Required CredentialsTypically a degree in health, science, or related field; certifications varyBachelor's or master's in food science, microbiology, or related
Work EnvironmentRegulatory agencies, laboratories, inspection sitesFood manufacturing facilities, laboratories, research settings
Employer & Industry UsageU.S. Food and Drug Administration, government agenciesFood companies, research institutions, government agencies
Common Search & Comparison IntentUnderstanding regulatory roles, compliance, and enforcementFood safety, product development, research

While both Fda professionals and Food Scientists work within the food industry, Fda roles focus on regulation, compliance, and enforcement of food safety laws, often within government agencies. Food Scientists primarily engage in research, product development, and ensuring food quality in manufacturing settings. The two careers overlap in food safety knowledge but differ in their primary responsibilities and work environments.

What qualifications do you need to work for the Food and Drug Administration?

To work for the Food and Drug Administration (FDA), candidates typically need a bachelor's degree in a relevant field such as science, engineering, or public health. For certain positions, advanced degrees or specialized certifications may be required, along with relevant work experience and knowledge of regulatory processes and compliance standards.

What are the most commonly searched types of Fda jobs in Miami, FL?

The most popular types of Fda jobs in Miami, FL are:

What are popular job titles related to Fda jobs in Miami, FL?

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

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

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

What cities near Miami, FL are hiring for Fda jobs?

Cities near Miami, FL with the most Fda job openings:

Fda jobs near you
Infographic showing various Fda job openings in Miami, FL as of August 2026, with employment types broken down into 90% Full Time, and 10% Contract. Highlights an 100% In-person job distribution, with an average salary of $76,246 per year, or $36.7 per hour.

DEA Compliance & Audit Readiness Consultant

Miami, FL

The FDA Group
Recruiting and Staffing Services • 11 - 50 employees
Learn more about The FDA Groupexternal

Full-time

Posted 11 days ago

Job description

DEA Compliance & Audit Readiness Consultant

Location: Onsite – North of Miami, Florida
Engagement Type: Consulting / Contract
Start: ASAP, with initial assessment targeted for early September
Duration: Through September, with potential ongoing support

Position Overview

We are seeking an experienced DEA Compliance & Audit Readiness Consultant to support a clinical research organization in South Florida. The consultant will conduct a comprehensive DEA Compliance Gap Assessment and Audit Readiness Review in preparation for an anticipated DEA inspection.

Following the initial assessment, the consultant may provide ongoing onsite support leading up to and potentially during the DEA inspection.

Key Responsibilities

  • Conduct an onsite DEA Compliance Gap Assessment/Audit Readiness Review.
  • Evaluate current controlled-substance practices and identify potential compliance gaps.
  • Assess organizational readiness for an upcoming DEA inspection.
  • Provide subject matter expertise related to Schedule I controlled substances used in clinical trials.
  • Provide guidance regarding Schedule II–V controlled substances.
  • Assess applicable compounding pharmacy requirements, particularly when an external compounding pharmacy supplies controlled substances or other drugs to the clinical trial site.
  • Provide practical recommendations and remediation guidance for identified compliance gaps.
  • Assist with inspection-readiness activities and preparation of site personnel.
  • Provide ongoing onsite compliance support, as needed, leading up to the DEA inspection.
  • Potentially provide onsite SME support during the DEA inspection.

Consultant Qualifications

  • Demonstrated experience with DEA compliance, audits, and/or DEA inspection readiness assessments.
  • Strong knowledge of federal controlled-substance requirements.
  • Experience or subject matter expertise involving Schedule I controlled substances, preferably within clinical research or clinical trial environments.
  • Knowledge of requirements applicable to Schedule II–V controlled substances.
  • Knowledge of regulatory requirements involving compounding pharmacies and controlled substances, including scenarios in which an external compounding pharmacy supplies drugs to a clinical trial site.
  • Experience conducting compliance gap assessments, mock inspections, audit readiness reviews, or similar regulatory assessments.
  • Ability to provide practical, hands-on remediation and inspection-readiness support.
  • Prior experience supporting or participating in DEA inspections is highly desirable.
  • Former FDA experience is a plus but is not required.

Location & Availability

This engagement requires onsite support north of Miami, Florida. Consultants located in the Fort Lauderdale/Miami/South Florida area are strongly preferred.

Candidates should be available to begin as soon as possible, with the initial DEA readiness assessment anticipated for early September and additional support potentially continuing through the end of September.