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Fda Regulatory Affairs Associate Jobs (NOW HIRING)

Robert Half

Regulatory Affairs Associate I

Skaneateles, NY · On-site

$25 - $30/hr

We are looking for a Regulatory Affairs Associate I to support global submission activities for medical device products from Skaneateles, New York. This Long-term Contract position offers a flexible ...

Arkray Group

Regulatory Affairs Associate

Plano, TX · On-site

Health Care / Regulatory & Clinical Support Position Title Junior or Assistant, Sales Support ... Support Sales and Marketing by helping address FDA compliance-related questions or concerns from ...

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Fda Regulatory Affairs Associate information

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How much do fda regulatory affairs associate jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for fda regulatory affairs associate in the United States is $39.57, according to ZipRecruiter salary data. Most workers in this role earn between $31.73 and $46.88 per hour, depending on experience, location, and employer.

What is an FDA Regulatory Affairs Associate?

FDA Regulatory Affairs Associates are professionals who ensure that companies comply with all regulations and laws set forth by the U.S. Food and Drug Administration (FDA) when developing, manufacturing, and marketing products such as pharmaceuticals, medical devices, and food items. They prepare and submit regulatory documents, communicate with regulatory agencies, and monitor changes in legislation to help guide their organization's compliance strategies. Their role is crucial to securing product approvals and maintaining ongoing compliance throughout the product lifecycle.

What are the key skills and qualifications needed to thrive as an FDA Regulatory Affairs Associate?

To thrive as an FDA Regulatory Affairs Associate, you need a solid understanding of regulatory guidelines, scientific principles, and a bachelor's degree in a life science or related field. Familiarity with regulatory submission systems (e.g., eCTD), document management tools, and knowledge of FDA regulations are typically required, and certification such as RAC can be advantageous. Strong attention to detail, problem-solving abilities, and clear written and verbal communication help professionals excel in this role. These skills are vital for ensuring compliance, minimizing approval delays, and facilitating successful product registrations with the FDA.

What are some common challenges faced by an FDA Regulatory Affairs Associate when preparing submissions?

FDA Regulatory Affairs Associates often encounter challenges such as interpreting evolving regulatory guidelines, coordinating data collection from cross-functional teams, and ensuring all submission documents are accurate and compliant with FDA requirements. Keeping up with frequent regulatory updates and communicating complex requirements to scientists and management can also be demanding. However, these challenges provide valuable experience in problem-solving and project management, which are essential for career advancement in regulatory affairs.

What is the difference between Fda Regulatory Affairs Associate vs Fda Regulatory Affairs Specialist?

AspectFda Regulatory Affairs AssociateFda Regulatory Affairs Specialist
CredentialsBachelor's degree in life sciences or related field; certifications like RAC are commonSimilar credentials; often holds RAC or advanced certifications
Work EnvironmentEntry-level role in pharmaceutical or biotech companies, regulatory agencies, or consulting firmsMid-level role with more independent responsibilities in similar settings
Employer & IndustryPharmaceutical, biotech, medical device companies, regulatory agenciesSame industries, with increased focus on compliance and submissions

The main difference is experience level and responsibility. Fda Regulatory Affairs Associates typically handle supporting tasks and document preparation, while Fda Regulatory Affairs Specialists take on more complex regulatory strategies and submissions. Both roles require similar credentials and work in comparable environments, but specialists usually have more independence and expertise.

What are popular job titles related to Fda Regulatory Affairs Associate jobs?

For Fda Regulatory Affairs Associate jobs, the most frequently searched job titles are:

Infographic showing various Fda Regulatory Affairs Associate job openings in the United States as of June 2026, with employment types broken down into 69% Full Time, and 31% Part Time. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $82,307 per year, or $39.6 per hour.

Regulatory Affairs Associate I

Clark, NJ • On-site

IntelliPro Group Inc.
Recruiting and Staffing Services • 201 - 500 employees
Learn more about IntelliPro Group Inc.external

$30 - $36/hr

Temporary

Re-posted 4 days ago

Job description

Job Title: Regulatory Affairs Associate I
Position Type: Contract (12+ Months)
Location: Clark, NJ 07066
Salary Rate: $30-36/hour
Job Description
We are seeking a detail-oriented Regulatory Affairs Associate I to support regulatory compliance activities for products distributed in the United States and Canada. This role will focus on reviewing product formulas and artwork for regulatory compliance, supporting product notification and registration processes, and maintaining documentation related to regulatory requirements.
The ideal candidate will have a science background, strong attention to detail, and the ability to manage multiple regulatory tasks in a fast-paced environment.
Responsibilities
  • Review product formulas to ensure compliance with US and Canada regulatory requirements
  • Review product artwork and labeling for regulatory compliance
  • Support product notification and registration processes in the US and Canada
  • Assist with Canada chemical regulatory oversight and compliance reviews
  • Prepare and maintain registration and regulatory documentation
  • Maintain and track KPIs related to product registration and notification processes
Requirements
  • Bachelor's degree in Science, Chemistry, or a related field
  • Coursework or certification in Cosmetic or Drug Regulatory Affairs preferred
  • Experience in the drug or cosmetic industry preferred
  • Ability to quickly learn new regulatory topics and coordinate multiple tasks
  • Strong organizational and communication skills
  • Proficiency with MS Office Suite
  • 0-3 years of professional experience
About Us
Founded in 2009, IntelliPro is a global leader in talent acquisition and HR solutions. Our commitment to delivering unparalleled service to clients, fostering employee growth, and building enduring partnerships sets us apart. We continue leading global talent solutions with a dynamic presence in over 160 countries, including the USA, China, Canada, Singapore, Japan, Philippines, UK, India, Netherlands, and the EU.
IntelliPro, a global leader connecting individuals with rewarding employment opportunities, is dedicated to understanding your career aspirations. As an Equal Opportunity Employer, IntelliPro values diversity and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, genetic information, disability, or any other legally protected group status. Moreover, our Inclusivity Commitment emphasizes embracing candidates of all abilities and ensures that our hiring and interview processes accommodate the needs of all applicants. Learn more about our commitment to diversity and inclusivity at https://intelliprogroup.com/.
Compensation: The pay offered to a successful candidate will be determined by various factors, including education, work experience, location, job responsibilities, certifications, and more. Additionally, IntelliPro provides a comprehensive benefits package, all subject to eligibility.

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