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 ...
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 ...
Regulatory Strategy, CMC, Labeling, Ad Promo, Medical Review, and Medical Information. Our team of senior-level leaders and innovators provides project-specific contributions or ongoing support ...
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Regulatory Strategy, CMC, Labeling, Ad Promo, Medical Review, and Medical Information. Our team of senior-level leaders and innovators provides project-specific contributions or ongoing support ...
Quality Regulatory Technician - Labeling Compliance Location: Miramar, FL Department: Quality Assurance / Regulatory Affairs Employment Type: Monday - Friday 8:30am - 5pm $19 - $22/ HR We are seeking ...
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Quality Regulatory Technician - Labeling Compliance Location: Miramar, FL Department: Quality Assurance / Regulatory Affairs Employment Type: Monday - Friday 8:30am - 5pm $19 - $22/ HR We are seeking ...
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 ...
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 ...
Regulatory Support Specialist
$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 ...
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Regulatory Support Specialist
$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 ...
Develops labeling specifications and approves proposed labeling, packaging, advertising and promotional materials after evaluating conformance to regulations * Plans schedules for regulatory ...
Develops labeling specifications and approves proposed labeling, packaging, advertising and promotional materials after evaluating conformance to regulations * Plans schedules for regulatory ...
Develops labeling specifications and approves proposed labeling, packaging, advertising and promotional materials after evaluating conformance to regulations * Plans schedules for regulatory ...
Develops labeling specifications and approves proposed labeling, packaging, advertising and promotional materials after evaluating conformance to regulations * Plans schedules for regulatory ...
Develops labeling specifications and approves proposed labeling, packaging, advertising and promotional materials after evaluating conformance to regulations * Plans schedules for regulatory ...
Develops labeling specifications and approves proposed labeling, packaging, advertising and promotional materials after evaluating conformance to regulations * Plans schedules for regulatory ...
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
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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
... labeling, packaging, advertising and promotional materials after evaluating conformance to regulations. Review, edit and provide regulatory and quality system approval for project documentation.
... labeling, packaging, advertising and promotional materials after evaluating conformance to regulations. Review, edit and provide regulatory and quality system approval for project documentation.
Regulatory Strategy, CMC, Labeling, Ad Promo, Medical Review, and Medical Information. Our team of senior-level leaders and innovators provides project-specific contributions or ongoing support ...
Quick apply
Regulatory Strategy, CMC, Labeling, Ad Promo, Medical Review, and Medical Information. Our team of senior-level leaders and innovators provides project-specific contributions or ongoing support ...
Regulatory Affairs Associate
Doral, FL · On-site
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 ...
Regulatory Affairs Associate
Doral, FL · On-site
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 ...
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 ...
Manager, Regulatory Affairs
Sunrise, FL · On-site
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 ...
Manager, Regulatory Affairs
Sunrise, FL · On-site
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 ...
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 ...
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 ...
Regulatory Compliance Spec./Food *2days Remote CoralGables
Miami, FL · On-site
$78K - $85K/yr
We are looking for a Regulatory Compliance Specialist to support product compliance, labeling accuracy, and certification standards for food products at a company in Miami FL. This position partners ...
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Regulatory Compliance Spec./Food *2days Remote CoralGables
Miami, FL · On-site
$78K - $85K/yr
We are looking for a Regulatory Compliance Specialist to support product compliance, labeling accuracy, and certification standards for food products at a company in Miami FL. This position partners ...
Senior QA Labeling Specialist
Fort Lauderdale, FL · On-site
$78K - $108K/yr
Create and modify label typography/typesetting for Life Extension. (Domestic / International), Wholesale customer labels and other private labels based on domestic regulations and branding guidelines.
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Senior QA Labeling Specialist
Fort Lauderdale, FL · On-site
$78K - $108K/yr
Create and modify label typography/typesetting for Life Extension. (Domestic / International), Wholesale customer labels and other private labels based on domestic regulations and branding guidelines.
Review and approve labels, claims, promotional materials, and compliance-sensitive content. * Ensure compliance with Health Canada, European Union, and other applicable international regulations.
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Review and approve labels, claims, promotional materials, and compliance-sensitive content. * Ensure compliance with Health Canada, European Union, and other applicable international regulations.
Review and approve labels, claims, promotional materials, and compliance-sensitive content. * Ensure compliance with Health Canada, European Union, and other applicable international regulations.
Review and approve labels, claims, promotional materials, and compliance-sensitive content. * Ensure compliance with Health Canada, European Union, and other applicable international regulations.
Regulatory Affairs Manager
Plantation, FL · On-site
... labeling, packaging, advertising and promotional materials after evaluating conformance to regulations. -Review, edit and provide regulatory and quality system approval for project documentation ...
Regulatory Affairs Manager
Plantation, FL · On-site
... labeling, packaging, advertising and promotional materials after evaluating conformance to regulations. -Review, edit and provide regulatory and quality system approval for project documentation ...
Regulatory Labeling information
See Florida salary details
$11.82 is the 25th percentile. Wages below this are outliers.
$9.70 - $15.30
66% of jobs
$15.30 - $20.90
6% of jobs
$23.24 is the 75th percentile. Wages above this are outliers.
$20.90 - $26.50
6% of jobs
$26.50 - $32.11
7% of jobs
$32.11 - $37.71
5% of jobs
$37.71 - $43.31
5% of jobs
$43.31 - $48.91
1% of jobs
$48.91 - $54.51
0% of jobs
$54.51 - $60.11
0% of jobs
$60.11 - $65.71
1% of jobs
$65.71 - $71.32
1% of jobs
$9
$22
$71
How much do regulatory labeling jobs pay per hour?
What is the difference between Regulatory Labeling vs Regulatory Documentation?
| Aspect | Regulatory Labeling | Regulatory Documentation |
|---|---|---|
| Purpose | Ensures 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 Environment | Primarily office-based, collaborating with marketing, legal, and regulatory teams. | Office and laboratory settings, often involving detailed technical writing and data compilation. |
| Required Credentials | Typically 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?
What are some common challenges faced in a Regulatory Labeling role, and how can they be managed?
What is a regulatory labeling specialist?
What is regulatory labeling?
What is regulatory labelling?
Which is better, RA or QA?
What is the highest paying job in regulatory affairs?
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Job 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.
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
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.
For more information contact me at (732) 4291635
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