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Assistant Regulatory Affairs Cosmetics Jobs in Decatur, GA

CorDx

Regulatory Affairs Manager (Atlanta)

Atlanta, GA · On-site

Regulatory Affairs Manager Location: Onsite - Atlanta, GA Position Summary: The Regulatory Affairs ... Stay current on changes in regulatory requirements and assist in assessing the impact on company ...

CorDx

Regulatory Affairs Manager (Atlanta)

Atlanta, GA · On-site

Regulatory Affairs Manager Location: Onsite - Atlanta, GA Position Summary: The Regulatory Affairs ... Stay current on changes in regulatory requirements and assist in assessing the impact on company ...

CorDx

Regulatory Affairs Manager (Atlanta)

Atlanta, GA · On-site

Regulatory Affairs Manager Location: Onsite - Atlanta, GA Position Summary: The Regulatory Affairs ... Stay current on changes in regulatory requirements and assist in assessing the impact on company ...

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All JobsRegulatory Affairs Cosmetics JobsAssistant Regulatory Affairs Cosmetics JobsAssistant Regulatory Affairs Cosmetics Jobs in Decatur, GA

Assistant Regulatory Affairs Cosmetics information

See Decatur, GA salary details

$15

$33

$142

How much do assistant regulatory affairs cosmetics jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for assistant regulatory affairs cosmetics in Decatur, GA is $33.78, according to ZipRecruiter salary data. Most workers in this role earn between $21.83 and $25.58 per hour, depending on experience, location, and employer.

What does an assistant regulatory affairs cosmetics do?

An Assistant Regulatory Affairs professional in the cosmetics industry supports regulatory compliance by helping ensure that cosmetic products meet all relevant laws and guidelines. This involves tasks such as preparing and reviewing product documentation, assisting with product registrations, monitoring changes in cosmetic regulations, and communicating requirements to internal teams. They often work closely with product development, quality assurance, and marketing departments to ensure products are safe and properly labeled before reaching the market.

What are the key skills and qualifications needed to thrive as an assistant regulatory affairs cosmetics?

To thrive as an Assistant Regulatory Affairs Cosmetics, you need a solid understanding of cosmetic regulations, product safety standards, and often a degree in a scientific discipline such as chemistry, biology, or pharmacy. Familiarity with regulatory databases, document management systems, and global compliance platforms like CPNP or FDA VCRP is typically required. Attention to detail, strong organizational skills, and effective communication are vital soft skills for managing documentation and collaborating with internal teams. These abilities ensure that products are compliant with regulations, reducing risk and supporting successful product launches.

What are the main challenges faced by an assistant regulatory affairs cosmetics?

One of the main challenges in this role is keeping up with the constantly evolving regulations and guidelines for cosmetic products across different regions. As an Assistant Regulatory Affairs professional, you’ll need to interpret and implement complex rules, often working under tight deadlines to ensure product compliance before launch. Collaboration with product development, marketing, and quality assurance teams is essential, as you’ll be responsible for reviewing ingredients, labeling, and documentation. Attention to detail and strong organizational skills are crucial to successfully navigate these challenges and support product compliance.

What is the difference between Assistant Regulatory Affairs Cosmetics vs Regulatory Affairs Specialist?

AspectAssistant Regulatory Affairs CosmeticsRegulatory Affairs Specialist
CredentialsBachelor's degree in life sciences or related field; often entry-level certificationsSame as assistant, but may require additional certifications or experience
Work EnvironmentSupportive, team-based, often in cosmetics or personal care companiesMore autonomous, responsible for compliance and submissions
ResponsibilitiesAssisting with documentation, research, and regulatory filingsPreparing submissions, ensuring compliance, liaising with authorities
Industry UsageCommonly found in cosmetics, personal care, and beauty companiesUsed across cosmetics, skincare, and related industries

While both roles require similar educational backgrounds and work in regulatory environments, the Assistant Regulatory Affairs Cosmetics typically supports senior staff with research and documentation, whereas the Regulatory Affairs Specialist handles more complex compliance tasks and submissions independently.

What are popular job titles related to Assistant Regulatory Affairs Cosmetics jobs in Decatur, GA?

For Assistant Regulatory Affairs Cosmetics jobs in Decatur, GA, the most frequently searched job titles are:

What job categories do people searching Assistant Regulatory Affairs Cosmetics jobs in Decatur, GA look for?

The top searched job categories for Assistant Regulatory Affairs Cosmetics jobs in Decatur, GA are:

What cities near Decatur, GA are hiring for Assistant Regulatory Affairs Cosmetics jobs?

Cities near Decatur, GA with the most Assistant Regulatory Affairs Cosmetics job openings:

Assistant Regulatory Affairs Cosmetics jobs near you
Infographic showing various Assistant Regulatory Affairs Cosmetics job openings in Decatur, GA as of June 2026, with employment types broken down into 74% Full Time, 17% Part Time, and 9% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $70,257 per year, or $33.8 per hour.

Regulatory Affairs Manager (Atlanta)

CorDx

Atlanta, GA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 13 days ago

Job description

Who is CorDx?
CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,100 employees across the world, serving millions of users in over 100 countries, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious disease such as COVID-19, pregnancy, drugs of abuse, biomarkers, and more. CorDx is at the cutting edge of technology, artificial intelligence, and data science with the goal of delivering diagnostic solutions to some of the most critical questions in healthcare.
Job Type: Full time
Job Title: Regulatory Affairs Manager
Location: Onsite - Atlanta, GA
Position Summary:
The Regulatory Affairs Manager will support the preparation, review, and submission of regulatory documentation for medical device products, ensuring compliance with applicable regulatory requirements including FDA, ISO 13485, and other global standards. This position collaborates with cross-functional teams to provide regulatory input during product development and throughout the product lifecycle, helping to secure timely product approvals and regulatory clearances.
Key Responsibilities:
  • Prepare, review, and coordinate the submission of regulatory documents including 510(k), technical files, and other filings to regulatory agencies.
  • Ensure product compliance with FDA regulations, ISO 13485, and applicable international standards.
  • Provide regulatory support to product development teams by offering guidance on applicable regulations and documentation requirements.
  • Stay current on changes in regulatory requirements and assist in assessing the impact on company processes and products.
  • Perform regulatory assessments for product changes and propose appropriate regulatory pathways.
  • Maintain documentation and records of all regulatory submissions and correspondence.
  • Support the preparation for regulatory agency meetings, audits, and inspections.
  • Collaborate with internal departments such as R&D, Quality, and Operations to ensure regulatory deliverables are met in a timely manner.

Requirements
Education:
  • Bachelor's degree in Regulatory Affairs, Life Sciences, Engineering, or a related field required.
  • Master's degree preferred.

Professional Experience:
  • 5-7 years of regulatory affairs experience within the medical device or IVD industry.
  • Working knowledge of 510(k) submissions and regulatory documentation processes.
  • Experience interacting with FDA and other regulatory agencies preferred.

Skills & Competencies:
  • Solid understanding of FDA regulations (21 CFR Part 820), ISO 13485, and medical device regulatory requirements.
  • Strong organizational and project management skills with the ability to manage multiple projects and priorities.
  • Excellent communication, problem-solving, and attention to detail.
  • Ability to work collaboratively in cross-functional teams and manage document workflows.

Benefits
  • Highly competitive compensation package.
  • Comprehensive medical, dental, and vision insurance.
  • 401(k) plan with generous company contributions.
  • Flexible paid time off (PTO) policy.
  • Additional substantial benefits.

Equal Opportunity Statement: We are an equal opportunity employer committed to inclusion and diversity. We do not discriminate based on race, gender, religion, sexual orientation, age, color, marital status, veteran status, disability status, national origin, or any other protected characteristic.

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