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Remote Regulatory Affairs Cosmetics Jobs (NOW HIRING)

Oscar Health

Analyst, Regulatory Affairs

Atlanta, GA · Remote

$28.30 - $37.15/hr

We're hiring a Analyst, Regulatory Affairs to join our Regulatory Affairs team. Oscar is the first ... This is a remote position, open to candidates who reside in: Atlanta, GA. You will be fully remote ...

Oscar Health

Analyst, Regulatory Affairs

Dallas, TX · Remote

$28.30 - $37.15/hr

We're hiring a Analyst, Regulatory Affairs to join our Regulatory Affairs team. Oscar is the first ... This is a remote position, open to candidates who reside in: Dallas, TX. You will be fully remote ...

Oscar Health

Analyst, Regulatory Affairs

Dallas, TX · Remote

$28.30 - $37.15/hr

We're hiring a Analyst, Regulatory Affairs to join our Regulatory Affairs team. Oscar is the first ... This is a remote position, open to candidates who reside in: Dallas, TX. You will be fully remote ...

Oscar Health

Analyst, Regulatory Affairs

Atlanta, GA · Remote

$28.30 - $37.15/hr

We're hiring a Analyst, Regulatory Affairs to join our Regulatory Affairs team. Oscar is the first ... This is a remote position, open to candidates who reside in: Atlanta, GA. You will be fully remote ...

Just Energy

Manager Regulatory Affairs

Austin, TX · Remote

Remote (Austin, Houston, Dallas, TX areas) Manager Title: Director of Regulatory Affairs, Mass Markets South (Texas, California, Canada) Position Overview The Regulatory Affairs Manager supports the ...

Dentsply Sirona

Regulatory Affairs Manager

This position can be a remote working arrangement. Candidates must be located in the US, ideally in the eastern time zone. Job Summary: The primary job responsibility for of the Regulatory Affairs ...

Dentsply Sirona, Inc

Regulatory Affairs Manager

This position can be a remote working arrangement. Candidates must be located in the US, ideally in the eastern time zone. Job Summary: The primary job responsibility for of the Regulatory Affairs ...

Cardinal Health

This is a remote position, and the ideal candidate will be located near or willing to travel to ... regulatory affairs experience preferred. * Experience in medical device industry a plus.

Mckesson

Regulatory Affairs Specialist

Concord, NC · Remote

This position is a US-based, full time, fully remote position; relocation assistance and ... regulatory affairs * Knowledge of medical terminology, FDA, other regulatory processes highly ...

Grid United

Director, Regulatory Affairs

$153K - $202K/yr

The roles will report to the Vice President of Regulatory Affairs and are open to remote candidates based in close proximity to relevant stakeholders. The Director of Regulatory Affairs will work ...

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Remote Regulatory Affairs Cosmetics information

See salary details

$15

$34

$145

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

As of Aug 6, 2026, the average hourly pay for remote 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 a remote regulatory affairs cosmetics specialist?

Remote Regulatory Affairs Cosmetics professionals are experts who ensure that cosmetic products comply with relevant regulations and safety standards while working from a remote location. They are responsible for reviewing product formulations, labeling, and marketing materials to ensure they meet the legal requirements of different countries or regions. These professionals often interact with regulatory agencies, stay updated on changing regulations, and help companies navigate the complex approval processes needed to bring cosmetic products to market. Working remotely, they use digital tools to collaborate with cross-functional teams and manage documentation. Their role is crucial in preventing costly compliance issues and ensuring consumer safety.

What are some common challenges faced by professionals in remote regulatory affairs for cosmetics, and how can they be addressed?

Professionals in remote regulatory affairs for cosmetics often encounter challenges such as staying up-to-date with frequently changing international regulations, managing communication across time zones, and ensuring accurate documentation without in-person oversight. To address these, it's important to establish clear communication channels with both internal teams and external regulatory bodies, utilize collaborative project management tools, and regularly participate in industry webinars or training. Maintaining strong organizational skills and building a network of global regulatory contacts can also help navigate the complexities of remote work in this field.

What are the key skills and qualifications needed to thrive as a remote regulatory affairs cosmetics specialist?

To excel as a Remote Regulatory Affairs Specialist in Cosmetics, you need a solid understanding of cosmetic regulations, scientific background (often in chemistry or related fields), and relevant experience in regulatory compliance. Familiarity with regulatory databases, labeling software, and global submission systems, as well as certifications such as RAC (Regulatory Affairs Certification), are highly valued. Strong attention to detail, effective communication, and the ability to collaborate virtually with cross-functional teams are crucial soft skills. These competencies ensure products meet legal requirements, avoid compliance risks, and support seamless market entry across different regions.

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

AspectRemote Regulatory Affairs CosmeticsRemote Quality Assurance Cosmetics
Required CredentialsRegulatory certifications, such as CCRA or RAPSQuality certifications, such as CQE or ISO auditor
Work EnvironmentCollaborates with regulatory agencies, product development teamsWorks with production, compliance, and audit teams
Industry UsageEnsures product compliance with regulationsMaintains quality standards and audits
Search & Comparison IntentUnderstanding regulatory roles in cosmeticsUnderstanding quality assurance roles in cosmetics

Remote Regulatory Affairs Cosmetics focuses on ensuring products meet legal and regulatory standards, while Remote Quality Assurance Cosmetics emphasizes maintaining product quality and compliance through audits and standards. Both roles are essential in the cosmetics industry but serve different functions related to compliance and quality management.

More about Remote Regulatory Affairs Cosmetics jobs
What cities are hiring for Remote Regulatory Affairs Cosmetics jobs? Cities with the most Remote Regulatory Affairs Cosmetics job openings:
What are the most commonly searched types of Regulatory Affairs Cosmetics jobs? The most popular types of Regulatory Affairs Cosmetics jobs are:
What states have the most Remote Regulatory Affairs Cosmetics jobs? States with the most job openings for Remote Regulatory Affairs Cosmetics jobs include:
What job categories do people searching Remote Regulatory Affairs Cosmetics jobs look for? The top searched job categories for Remote Regulatory Affairs Cosmetics jobs are:
Remote Regulatory Affairs Cosmetics jobs near you
Infographic showing various Remote Regulatory Affairs Cosmetics job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 9% Part Time, and 4% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $71,960 per year, or $34.6 per hour.

Remote Regulatory Affairs contractor

Globalchannelmanagement

Atlanta, GA • Remote

$99 - $100/hr

Full-time

Re-posted 10 days ago

Job description

Remote Regulatory Affairs contractor requires:

  • Bachelor's degree in engineering, life sciences, regulatory affairs, legal or a related field
  • 5-10 years+ of global medical device regulatory experience
  • Proven experience preparing, writing and submitting FDA 510k submissions (end to end)
  • Experience with ophthalmic devices, capital equipment, diagnostic devices, software in medical devices, cybersecurity
  • Strong working knowledge of:
    • FDA regulations (21 Parts 807, 820)
    • FDA guidance documents and eStar requirements
    • Experience with Canadian regulations, EU MDR (2017/745) including Class lla, Tech docs Annex ll/lll
  • Demonstrated ability to work independently as a contractor in a fast-paced environment
  • Experience filing medical device submissions in China and other countries
  • Experience with audiology devices
  • Experience with artificial-intelligence enabled devices
  • Strong technical writing and documentation skills
  • Ability to translate complex technical information into regulatory submissions
  • Detail-oriented with strong organization skills
  • Effective communicator across technical and non-technical stakeholders
  • Ability to manage multiple deliverables and timelines

DUTIES:

  • FDA 510(k) submission
  • Conduct comprehensive review of technical documentation (design controls, V&V, risk, labeling, clinical evidence, and software as applicable) to ensure completeness, quality, and regulatory compliance
  • Perform detailed regulatory gap assessments against FDA requirements (21 CFR Parts 807, 820, and applicable FDA guidance documents)
  • Author, compile and deliver a complete 510k submission, including preparation in FDA eSTAR format,
  • Lead submission lifecycle activities, including:
    • Acceptance Review support (RTA readiness)
    • Substantive Review coordination
    • Drafting and submission of responses to FDA requests for Additional Information, Interactive review communications
    • Updating submission content and modules as required
  • Interface cross-functionally to incorporate Business inputs and ensure alignment throughout the review process.
  • Provide regulatory leadership through FDA clearance.
  • EU MDR Technical Documentation Support
  • Conduct EU MDR readiness assessment aligned with Notified Body expectations and conformity assessment requirements.
  • Perform critical review and gap analysis of EU MDR technical file
  • Provide targeted recommendations to ensure audit-readiness and Notified Body acceptance
  • Lead or support submission to obtain CE Mark
  • Health Canada submission
  • Global Regulatory Strategy and Advisory