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Fda Compliance Consultant Jobs (NOW HIRING)

Alston & Bird is seeking an experienced FDA consultant to work with the Health Care team's FDA ... Minimum of 5 years as an FDA investigator or compliance officer, or industry senior position in ...

$100 - $125/hr

Consultant, Food Safety and Quality Assurance Intertek Alchemy is seeking a Consultant to join our ... Support clients in addressing USDA‑FSIS and FDA compliance requirements, including responses to ...

New

IT Compliance Analyst

Seattle, WA · On-site

$60 - $80/hr

Consulting Firms: Specialized compliance consultancies serving multiple industries and regulatory ... Boston, Philadelphia, Research Triangle with specialized HIPAA and FDA requirements * Government ...

WI · On-site

$125 - $150/hr

Ensure compliance with FDA, cGMP, GAMP 5, ALCOA+, and 21 CFR Part 11 requirements. * Collaborate with Automation, Engineering, IT, Manufacturing, and Quality teams during project execution. * Support ...

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Fda Compliance Consultant information

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$35.5K

$80.9K

$148.5K

How much do fda compliance consultant jobs pay per year?

As of Sep 8, 2026, the average yearly pay for fda compliance consultant in the United States is $80,929.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,000.00 and $96,500.00 per year, depending on experience, location, and employer.

What is the difference between Fda Compliance Consultant vs Quality Assurance Specialist?

AspectFda Compliance ConsultantQuality Assurance Specialist
CredentialsRelevant certifications (e.g., RAC, CQE), industry experienceQuality certifications (e.g., ASQ CQE, ISO auditor), industry experience
Work EnvironmentConsulting firms, pharmaceutical, medical device companiesManufacturing plants, laboratories, healthcare companies
Employer & Industry UsageAdvises on FDA regulations complianceEnsures product quality and compliance in production
Search & Comparison IntentUnderstanding regulatory compliance rolesQuality management and process improvement

While both roles focus on compliance, an Fda Compliance Consultant primarily advises companies on FDA regulations and ensures regulatory adherence, often working as a consultant. A Quality Assurance Specialist focuses on maintaining product quality within manufacturing or lab environments, implementing quality systems and procedures. Both roles require industry-specific certifications and experience, but their core responsibilities differ in scope and focus.

What states have the most Fda Compliance Consultant jobs?

States with the most job openings for Fda Compliance Consultant jobs include:

What are popular job titles related to Fda Compliance Consultant jobs?

For Fda Compliance Consultant jobs, the most frequently searched job titles are:

Infographic showing various Fda Compliance Consultant job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 84% Full Time, 11% Part Time, and 4% Contract. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $80,929 per year, or $38.9 per hour.

DEA Compliance & Audit Readiness Consultant

The FDA Group

Miami, FL • On-site

Full-time

Posted 21 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.