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Fda Consulting Jobs in Florida (NOW HIRING)

Apex Systems

Validation Engineer

Riverview, FL · On-site

Ensure compliance with FDA regulations, GMP requirements, and internal quality standards. Required ... Everforth Apex has a dedicated customer service team for our Consultants that can address questions ...

Software People, Inc.

Microsoft Azure Admin

Tallahassee, FL · On-site

$52.25 - $64.75/hr

... consultant is required to have professional working experience at an advance level to carry out the ... Communicate orally and in writing to FDA customers and application teams. * Support the production ...

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How much do fda consulting jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for fda consulting in Florida is $39.24, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $52.12 per hour, depending on experience, location, and employer.

What is an FDA consulting?

An FDA Consulting job involves providing expert guidance to businesses seeking regulatory approval for their products from the U.S. Food and Drug Administration (FDA). Consultants help companies navigate complex FDA regulations, ensure compliance, and prepare necessary documentation for submissions. They may work with pharmaceuticals, medical devices, food, and biotech industries. Their role includes strategy development, risk assessment, and communication with the FDA to facilitate approvals and avoid compliance issues.

What does an FDA consultant do?

As an FDA Consultant, your day might involve reviewing regulatory documentation, preparing submissions for FDA approval, and advising clients on compliance strategies. You’ll often attend meetings with cross-functional teams including R&D, quality assurance, and legal experts to ensure alignment on regulatory requirements. Consultants also stay updated on changes in FDA guidelines, draft correspondence to regulatory agencies, and address client questions or concerns. This dynamic role requires adaptability and strong collaboration skills to manage multiple projects and effectively support clients through all stages of the regulatory process.

What skills and qualifications are needed for FDA consulting?

To thrive in FDA Consulting, you need expertise in regulatory affairs, a deep understanding of FDA guidelines, and often a degree in life sciences or a related field. Familiarity with regulatory submission systems such as eCTD, knowledge of GxP standards, and certifications like RAC (Regulatory Affairs Certification) are valuable. Strong communication, analytical thinking, and project management skills set outstanding consultants apart. These competencies are essential to effectively guide clients through complex regulatory landscapes and ensure successful product approvals.

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Fda Consulting jobs near you
Infographic showing various Fda Consulting job openings in Florida as of August 2026, with employment types broken down into 1% Internship, 84% Full Time, 10% Part Time, and 5% Contract. Highlights an 83% Physical, 6% Hybrid, and 11% Remote job distribution, with an average salary of $81,624 per year, or $39.2 per hour.

Global Regulatory Compliance Specialist

Life Extension Foundation Buyers Club Inc

Fort Lauderdale, FL • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

This position provides expertise and is responsible for managing all documentation and regulatory reviews for expansion of Life Extension products globally. Collaborates with different functional areas (Purchasing, Product Development) and external consultants to provide regulatory compliance feedback during various steps of the product launch process as well as review of existing product reformulation for global expansion.

Core Duties and Responsibilities:

  • Create and maintain product dossiers as required to support international business
  • Oversee, prepare, and manage various submissions and responses to regulatory authority questions ensuring adherence to national and international regulations and standards (i.e., FDA, Health Canada, European Union)
  • Assist with regulatory review of current product formulations to ensure compliance with international requirements for current active projects
  • Work with suppliers to ensure documentation and product requirements are met for international market entry
  • Communicate effectively across several different functional areas including internal cross-functional teams (purchasing, product development, marketing) and external vendors (consultants, contract manufacturers, raw material suppliers)
  • Serve as a liaison with external consulting firms engaged in activities related to international compliance, labelling, or product registration
  • Provide global regulatory oversight and compliance feedback for new item concepts and reformulation of existing items
  • Review proposed labelling to ensure intended use and claims are supported and domestic and international regulations are met
  • Organize and manage status of all in-process regulatory projects
  • Organize and track product registrations when approval from governing authorities has been received
  • Help develop and maintain a regulatory database
  • Assist with US Regulatory inquires when needed
  • 2 onsite days per week is an essential function of this position
  • Additional duties as needed

Position Requirements:

  • Bachelor’s degree (or equivalent) in science or health-related field
  • 2+ years of dietary supplement experience or equivalent within a Quality or Regulatory Affairs environment; demonstrated knowledge of international regulations strongly preferred
  • Baseline understanding of US regulations and labelling requirements
  • Ability to interact with associates on all levels and communicate effectively across several functional areas
  • Strong organization skills and detail oriented
  • Excellent communication skills; verbal and written, including technical writing
  • Ability to translate highly technical information so it is understandable for the target audience