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Entry Level Regulatory Affairs Cosmetics Jobs (NOW HIRING)

Collaborative LLC

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Entry-Level Regulatory Affairs Associate

South Portland, ME · On-site

$20 - $23/hr

Entry-Level Regulatory Affairs Associate Location: South Portland, ME Pay: $20-$23 per hour Schedule: Monday-Friday, 7:00 AM-4:30 PM We are seeking an Entry-Level Regulatory Affairs Associate to ...

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MWI Animal Health

NY · On-site

$68.51 - $102.76/hr

## Regulatory Affairs ManagerPostulerlocations: NCEE > Poland > Remotetime type: Temps Pleinposted on ... cosmetics, food supplements, and herbal products, helping clients navigate Polish regulatory ...

World Courier

NY · On-site

$47.48 - $79.14/hr

... cosmetics, food supplements, and herbal products, helping clients navigate Polish regulatory ... The Regulatory Affairs Manager - Poland is responsible for managing regulatory activities and ...

PrideStaff

Regulatory Affairs Associate

Tustin, CA · On-site

$32 - $36/hr

The Regulatory Affairs Associate is an entry-level position for an individual committed to developing a career in Regulatory Affairs. The role supports Regulatory Affairs activities primarily for the ...

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Better Being Co.

$85 - $115/hr

Job Summary The Regulatory Affairs Scientist reviews dietary supplements, cosmetic, and beverage labels and formulas for compliance; creates and maintains ingredient specifications; and coordinates ...

Zymo Research

Regulatory Affairs Associate

Tustin, CA · On-site

$68 - $75/hr

The Regulatory Affairs Associate is an entry-level position for an individual committed to developing a career in Regulatory Affairs. The role supports Regulatory Affairs activities primarily for ...

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Entry Level Regulatory Affairs Cosmetics information

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$15

$34

$145

How much do entry level regulatory affairs cosmetics jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for entry level regulatory affairs cosmetics in the United States is $34.60, according to ZipRecruiter salary data. Most workers in this role earn between $22.36 and $26.20 per hour, depending on experience, location, and employer.

What is an entry level regulatory affairs professional in cosmetics?

Entry level regulatory affairs roles in cosmetics involve assisting with ensuring that cosmetic products comply with all relevant laws, regulations, and guidelines before they reach the market. Professionals in these positions help prepare and review product labeling, maintain regulatory documentation, and communicate with regulatory agencies. They often support senior staff in keeping up-to-date with changes in cosmetic regulations and ensuring that new products meet all compliance requirements. These roles are ideal for individuals interested in the intersection of science, law, and product development.

What does an entry level regulatory affairs professional in cosmetics do?

In an entry level regulatory affairs role within the cosmetics industry, you can expect to spend your days assisting with the preparation and review of product labels, ingredient lists, and safety data to ensure compliance with relevant regulations. You may also support the submission process for new products, monitor regulatory changes, and help maintain documentation required for audits. Collaboration is common with product development, marketing, and quality assurance teams to address compliance questions and keep everyone informed of regulatory requirements.

What skills and qualifications are needed to thrive as an entry level regulatory affairs professional in cosmetics?

To thrive as an Entry Level Regulatory Affairs professional in cosmetics, you need a background in life sciences or a related field, attention to detail, and an understanding of cosmetic regulations. Familiarity with regulatory databases, ingredient safety assessment tools, and documentation systems is typical, while knowledge of international regulations (like FDA or EU Cosmetic Regulation) is beneficial. Strong organizational skills, effective communication, and the ability to collaborate across teams help you excel in this role. These skills ensure compliance, facilitate timely product launches, and help protect both consumer safety and the company’s reputation.

What is the difference between Entry Level Regulatory Affairs Cosmetics vs Entry Level Quality Assurance Cosmetics?

AspectEntry Level Regulatory Affairs CosmeticsEntry Level Quality Assurance Cosmetics
Required CredentialsBachelor's in life sciences, certifications like RAPS or regulatory coursesBachelor's in sciences, quality assurance certifications preferred
Work EnvironmentRegulatory agencies, corporate compliance teamsManufacturing facilities, quality control labs
Industry UsageEnsures product compliance with regulationsMaintains product quality and safety standards

While both roles support cosmetic product safety, Regulatory Affairs focuses on compliance with regulations, whereas Quality Assurance emphasizes product quality and safety standards. Entry Level Regulatory Affairs Cosmetics professionals handle regulatory submissions and documentation, while Quality Assurance roles involve testing and process audits. Both are essential for bringing safe, compliant cosmetic products to market.

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Entry Level Regulatory Affairs Cosmetics jobs near you
Infographic showing various Entry Level Regulatory Affairs Cosmetics job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 9% Part Time, and 2% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $71,960 per year, or $34.6 per hour.

Entry-Level Regulatory Affairs Associate

Collaborative LLC

South Portland, ME • On-site

$20 - $23/hr

Full-time

Medical, Dental, Vision

Posted 3 days ago

New

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Job description

Entry-Level Regulatory Affairs Associate

Location: South Portland, ME
Pay: $20–$23 per hour
Schedule: Monday–Friday, 7:00 AM–4:30 PM


We are seeking an Entry-Level Regulatory Affairs Associate to support regulatory activities in a medical device environment.


This is an excellent opportunity for someone who is new to Regulatory Affairs and wants to build experience in a highly regulated industry. The ideal candidate is organized, detail-oriented, comfortable working with documents and computer systems, and able to follow procedures accurately.


Prior Regulatory Affairs experience is not required.


Job Summary

  • Assist with organizing and preparing regulatory documents and submission materials
  • Support the preparation of regulatory submission and registration packages
  • Review documents for accuracy, completeness, and consistency
  • Maintain electronic and paper regulatory records
  • Track regulatory requests, submissions, and project timelines
  • Assist with updating product listings, registrations, licenses, and approvals
  • Help prepare routine regulatory reports and communications
  • Research regulatory requirements and procedures as directed
  • Assist with document quality control
  • Maintain tracking and document management systems
  • Support post-market regulatory activities
  • Prepare and organize documentation for registrations and other regulatory purposes
  • Work with internal teams to gather and organize required information
  • Follow established procedures, templates, and regulatory guidelines
  • Help ensure regulatory activities are completed accurately and on schedule


Qualifications

  • High school diploma or equivalent required
  • Approximately 1 year of work experience preferred
  • No prior Regulatory Affairs experience required
  • Strong attention to detail and organizational skills
  • Ability to work with detailed documents and information
  • Strong written and verbal communication skills
  • Comfortable using computers and electronic document systems
  • Ability to follow procedures and instructions carefully
  • Ability to manage multiple tasks and meet deadlines


Ideal Backgrounds

Candidates with experience in the following areas may be a strong fit:

  • Quality Control or Quality Assurance
  • Document Control or Documentation
  • Administrative or Records Support
  • Medical Device or Pharmaceutical Manufacturing
  • Manufacturing or Production
  • Healthcare or Clinical Support
  • Laboratory environments
  • Data Entry or detail-oriented office roles


Experience working with SOPs, controlled documents, records, quality processes, compliance requirements, or tracking systems is a plus.


If you have a strong attention to detail and are looking to begin a career in Regulatory Affairs, Quality, or a related field, apply today!