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Regulatory Labeling Jobs in Florida (NOW HIRING)

These interpretations are used for every aspect of the regulatory discipline from submissions to labeling issues. * Demonstrated the ability to develop global regulatory strategies for high risk ...

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

... labeling, packaging, advertising and promotional materials after evaluating conformance to regulations. Review, edit and provide regulatory and quality system approval for project documentation.

Participate in pre-/post-market regulatory activities as assigned (labeling review/approval, FDA submission support, consultant coordination, and 510(k) support with R&D). * Support product launch ...

Participate in pre-/post-market regulatory activities as assigned (labeling review/approval, FDA submission support, consultant coordination, and 510(k) support with R&D). * Support product launch ...

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Regulatory Labeling information

See Florida salary details

$9

$22

$71

How much do regulatory labeling jobs pay per hour?

As of Jul 26, 2026, the average hourly pay for regulatory labeling in Florida is $22.81, according to ZipRecruiter salary data. Most workers in this role earn between $12.93 and $29.28 per hour, depending on experience, location, and employer.

What is the difference between Regulatory Labeling vs Regulatory Documentation?

AspectRegulatory LabelingRegulatory Documentation
PurposeEnsures product labels meet regulatory standards and communicate necessary information to consumers and authorities.Prepares comprehensive reports, submissions, and records required for regulatory approval and compliance.
Work EnvironmentPrimarily office-based, collaborating with marketing, legal, and regulatory teams.Office and laboratory settings, often involving detailed technical writing and data compilation.
Required CredentialsTypically requires a degree in life sciences, regulatory affairs, or related fields; certifications like RAC are common.Similar credentials, often with advanced degrees or certifications in regulatory affairs or quality assurance.

While both roles focus on compliance, Regulatory Labeling concentrates on product labels and packaging, ensuring they meet legal standards. Regulatory Documentation involves creating detailed reports and submissions for regulatory approval. Both roles require similar qualifications and often work together to ensure product compliance throughout the development and marketing process.

What are the key skills and qualifications needed to thrive as a Regulatory Labeling Specialist, and why are they important?

To thrive as a Regulatory Labeling Specialist, you need a strong understanding of regulatory requirements, scientific knowledge, and experience with labeling guidelines, often supported by a life sciences degree. Familiarity with regulatory submission systems (such as FDA’s SPL), document management tools, and relevant certifications like RAC are typically required. Attention to detail, effective communication, and project management skills help ensure accuracy and collaboration across teams. These competencies are critical to producing compliant, clear, and timely product labeling that meets global regulatory standards.

What are some common challenges faced in a Regulatory Labeling role, and how can they be managed?

Professionals in Regulatory Labeling often encounter challenges such as keeping up with constantly changing global regulations, coordinating input from multiple departments, and ensuring labeling accuracy across different markets. Managing these challenges typically involves maintaining strong communication with regulatory affairs, legal, and product development teams, as well as staying updated through regulatory databases and ongoing training. Leveraging project management tools and establishing clear review processes can also help ensure labeling compliance and timely submissions.

What is a regulatory labeling specialist?

A regulatory labeling specialist is a professional responsible for developing, reviewing, and maintaining product labels to ensure compliance with industry regulations and standards. They often work with regulatory agencies, use labeling software, and stay updated on legal requirements to ensure accurate and compliant product information.

What is regulatory labeling?

Regulatory labeling refers to the process of creating, reviewing, and maintaining product labels to ensure they comply with all relevant laws and regulations set by government authorities. This is especially important in industries like pharmaceuticals, food, and chemicals, where product labels must accurately reflect usage instructions, safety information, and legal requirements. Regulatory labeling professionals work closely with regulatory agencies and internal teams to make sure that all product information is truthful, clear, and up to date. Failure to comply with labeling regulations can result in fines, product recalls, or legal action.

What is regulatory labelling?

Regulatory labeling involves creating and maintaining product labels that comply with government regulations and industry standards. It ensures that product information such as safety warnings, ingredients, and usage instructions meet legal requirements, often requiring attention to detail and knowledge of relevant regulations. Regulatory labelers may work with documentation tools and certification processes to ensure compliance.

Which is better, RA or QA?

Regulatory Affairs (RA) and Quality Assurance (QA) are distinct roles in the compliance and quality management of products. RA focuses on ensuring products meet regulatory requirements and preparing documentation for approval, while QA emphasizes maintaining product quality through testing and process controls. Both roles are essential, and their importance depends on the company's priorities and product lifecycle stage.

What is the highest paying job in regulatory affairs?

The highest paying roles in regulatory affairs are typically senior executive positions such as Vice President or Director of Regulatory Affairs, which can earn six-figure salaries. These roles often require extensive experience, advanced certifications, and leadership skills in managing compliance strategies across industries like pharmaceuticals and medical devices.
What are the most commonly searched types of Regulatory Labeling jobs in Florida? The most popular types of Regulatory Labeling jobs in Florida are:
Infographic showing various Regulatory Labeling job openings in Florida as of July 2026, with employment types broken down into 1% As Needed, 74% Full Time, 20% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 97% Physical, and 3% Remote job distribution, with an average salary of $47,448 per year, or $22.8 per hour.
Regulatory Labeling Associate

Regulatory Labeling Associate

Integrated Resources INC

Jacksonville, FL

Other

Posted 26 days ago


Job description

Company Description

A Few Words About Us
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

The Regulatory Labeling Associate provides support to the Global Regulatory Affairs Labeling Center of Excellence (LCoE) team by supporting labeling content and artwork development activities for new products as well as updates to existing product labeling.

The Regulatory Labeling Associate will:

Master Complexity

Autonomy

Works independently on routine tasks;

Requires some supervision on non-routine tasks.

Managing complexity/Technical accountability

Demonstrates technical competency to perform job function;

Demonstrates compliance with departmental operations;

Demonstrates knowledge of current regulations and standards.

Innovation

Continuous Learning/Managing Risk

Demonstrates a systematic approach to solving problems.

Fueling Business Growth/Impact on Systems & Practices

Identifies and implements improvements on work assignments.

Customer Focus

Delivery of results/Customer value

Is proactive in fulfilling customer requirements.

Interdependent Partnering

Team Contribution

Completes technical tasks on work teams.


Relationship skills

Interacts effectively with peers and supervisors.

Organizational & People Development

Developing Others

Responsible for individual development

Creating the environment

Contributes to day-to-day harmony within the group;

Adapts to changing priorities.

CREDO

Adheres to environmental policy and procedures and supports department environmental objectives.


 ESSENTIAL FUNCTIONS / RESPONSIBILITIES

Assists in reviewing, analyzing, and evaluating proposed worldwide labeling including, but not limited to, packaging, instructions for use, and investigational/clinical labeling for accuracy against established standards.

Conducting required research including part number and copy clearance verification, historical submission information, competitive labeling intelligence, etc.

Document/artwork formatting to support copy clearance, review, and submission documentation.

Facilitating and tracking electronic document and artwork submissions in internal systems.

Gathering and analyzing data related to labeling processes, errors, and efficiencies and preparing associated metrics reports.

Other activities and tasks to support the LCoE or Global Regulatory Affairs department, as assigned by management.

Qualifications

QUALIFICATIONS

High school diploma required, Bachelor's degree preferred.

Minimum experience (number of month/years and type of work experience beyond formal education) required for competent performance:

0 years with bachelor's degree or 3 years of prior operations, RA, QA or R&D experience preferred.

Past labeling or artwork development experience preferred.

Flexibility to work on multiple projects; ability to collect and analyze published material; familiarity with regulatory submissions, ability to develop innovative solutions to problems with limited complexity; keen attention to detail; very good organizational, communication and interpersonal skills; ability to work in a cross-functional team environment and provide quality customer service.

Familiarity/working knowledge of the following software programs (Required):

Microsoft Outlook


Microsoft Word


Microsoft Excel


Microsoft PowerPoint


Adobe Acrobat Professional


Additional preferred software program experience includes:

Adobe InDesign


Adobe Illustrator


SUPERVISION / AUTHORITY

Give no supervision to others.


Have lead responsibilities for one or more employees.


Responsible for work flow production, training of new employees on covered jobs, answering job-related questions in one or more areas.


In addition, assist in reporting on performance, recommending advancements, implementing new or changed procedures. Generally recognized as Group Leader or Assistant Supervisor.


Have full, direct supervisory responsibilities for a department or function.


Feel free to forward my email to your friends/colleagues who might be available.

Additional Information

For more information contact me at  (732) 4291635



Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996