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Fda Contract Jobs in Florida (NOW HIRING)

Competitive contract rate, commensurate with experience * Opportunity to play a key role in a growing, FDA-regulated consumer health products company * Collaborative, fast-paced environment with ...

Competitive contract rate, commensurate with experience * Opportunity to play a key role in a growing, FDA-regulated consumer health products company * Collaborative, fast-paced environment with ...

Temporary Contract (15 Weeks) Schedule: Monday - Friday | 8:30 AM - 5:00 PM Pay: $41.00 - $56.00 ... Ensure compliance with FDA regulations, Good Clinical Practice (GCP), IRB requirements, and sponsor ...

Competitive contract rate, commensurate with experience * Opportunity to play a key role in a growing, FDA-regulated consumer health products company * Collaborative, fast-paced environment with ...

Contract (15 Weeks) Schedule: Monday - Friday, 8:30 AM - 5:00 PM Pay: $32.00 - $43.00 per hour Job ... Ensure compliance with FDA, IRB, GCP, and sponsor requirements. * Prepare for sponsor visits ...

Quality Manager

Holly Hill, FL ยท On-site

$50K - $80K/yr

Ensure all activities align with FDA, industry standards, and applicable international regulations. Qualifications * 5+ years of quality assurance or quality management experience in contract ...

R&D Formulator - Liquid Nutritional Products | Contract Manufacturing | Onsite Position Summary ... Ensure compliance with FDA, cGMP, and labeling standards ยท Maintain accurate formulas ...

Quality Stablity Specialist

Miami, FL ยท On-site

$26 - $28/hr

... an FDA approved, state-of-the art manufacturing facility in Miami, FL. This is a contract - to - permanent opportunity (based on performance) and the pay rate is $26 - $28 an hour. If you are ...

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Fda Contract information

See Florida salary details

$30.6K

$79.2K

$103.9K

How much do fda contract jobs pay per year?

As of Aug 31, 2026, the average yearly pay for fda contract in Florida is $79,238.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,500.00 and $88,900.00 per year, depending on experience, location, and employer.

What is an Fda contract?

An FDA Contract job refers to a temporary or project-based position working with or for the U.S. Food and Drug Administration (FDA) through a contractual agreement. These roles can be with the FDA directly or through third-party contractors supporting FDA initiatives. Responsibilities may include regulatory compliance, data analysis, scientific research, IT support, or administrative tasks. Contract positions vary in duration and benefits but provide opportunities to work in a highly regulated environment.

What are the primary responsibilities of someone working under an Fda contract?

As an FDA Contract professional, your primary responsibilities usually include developing, reviewing, and managing documents and agreements in accordance with FDA guidelines and regulations. You may coordinate closely with regulatory affairs, legal, and project management teams to ensure that all contract terms support compliance and meet project timelines. Daily tasks might involve drafting and negotiating contract language, tracking deliverables, and supporting regulatory submissions. This role is both detail-oriented and collaborative, and it provides valuable experience for those seeking advancement into regulatory management or specialist positions.

What are the key skills and qualifications needed to thrive in the Fda contract position, and why are they important?

To thrive in an FDA Contract role, you need strong knowledge of FDA regulations, compliance processes, and contract management, often supported by a background in life sciences or regulatory affairs. Familiarity with tools such as Document Control Systems, eCTD publishing software, and experience with regulatory submission platforms are typically required. Outstanding attention to detail, negotiation skills, and the ability to collaborate across cross-functional teams help candidates excel. These competencies are critical for ensuring contracts meet strict regulatory standards and for navigating the complexities of FDA approval and compliance procedures.

What are the most commonly searched types of Fda jobs in Florida?

The most popular types of Fda jobs in Florida are:

What are popular job titles related to Fda Contract jobs in Florida?

For Fda Contract jobs in Florida, the most frequently searched job titles are:

What cities in Florida are hiring for Fda Contract jobs?

Cities in Florida with the most Fda Contract job openings:

Infographic showing various Fda Contract job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, 3% Contract, and 1% Nights. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $79,238 per year, or $38.1 per hour.

DEA Compliance & Audit Readiness Consultant

The FDA Group

Miami, FL

Full-time

Posted 13 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.