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Remote Regulatory Affairs Jobs (NOW HIRING)

As a fully remote company, we lead with clear communication, accountability, and trust, and we give ... Reporting to the Regulatory Affairs Manager, you'll help ensure our labels, claims, and promotional ...

This role oversees Regulatory Affairs personnel and ensures effective execution of U.S. and international regulatory activities, including regulatory submissions, inspections and audits, recalls ...

This role oversees Regulatory Affairs personnel and ensures effective execution of U.S. and international regulatory activities, including regulatory submissions, inspections and audits, recalls ...

This role oversees Regulatory Affairs personnel and ensures effective execution of U.S. and international regulatory activities, including regulatory submissions, inspections and audits, recalls ...

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Remote Regulatory Affairs information

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$39

$62

How much do remote regulatory affairs jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for remote regulatory affairs 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 remote regulatory affairs?

Remote regulatory affairs refer to professionals who ensure that companies comply with regulations and laws governing their industry, such as pharmaceuticals, medical devices, or food, while working from a location outside of the traditional office environment. These roles involve preparing and submitting regulatory documents, communicating with regulatory agencies, and keeping up-to-date with changing laws—all performed virtually. Remote regulatory affairs specialists use digital tools to collaborate with teams and manage compliance tasks efficiently. This type of work offers flexibility and allows organizations to tap into a wider talent pool regardless of geographic location.

What are the qualifications to get a remote regulatory affairs job?

The qualifications to get a remote regulatory affairs job typically include a bachelor’s or master’s degree and some previous experience in regulatory affairs. Your degree should be in a subject related to your work. For example, if you work in pharmaceutical regulatory affairs, you should have a degree in pharmacy, biology, chemistry, or a closely related field. Working in pesticide manufacturing requires a degree in chemical engineering or chemistry. You should also have strong writing skills to develop policy documents and the ability to understand how state, national, and international regulations affect your industry. Interpersonal and networking skills are a plus. Being bilingual or multilingual is useful. To work from home, you must have a reliable internet connection and basic computer proficiency.

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

To thrive as a Remote Regulatory Affairs professional, you need a solid understanding of regulatory guidelines, compliance standards, and industry-specific legislation, often supported by a degree in life sciences or a related field. Familiarity with regulatory submission platforms, document management systems, and certifications such as RAC (Regulatory Affairs Certification) are highly valuable. Strong attention to detail, effective written and verbal communication, and the ability to collaborate across global teams are crucial soft skills. These competencies ensure accurate compliance with regulations, efficient submission processes, and successful product approvals in a remote work environment.

How does working remotely in regulatory affairs impact collaboration with cross-functional teams?

Remote Regulatory Affairs professionals often collaborate with teams such as clinical, quality, and legal departments spread across multiple locations. Effective communication is essential, typically facilitated through video meetings, project management tools, and shared digital documentation. While remote work offers flexibility, it can sometimes present challenges in coordinating across time zones and ensuring alignment on compliance deadlines. Proactively scheduling regular check-ins and maintaining clear, organized records helps foster strong collaboration and keeps regulatory projects on track.

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

AspectRemote Regulatory AffairsRemote Quality Assurance
Required CredentialsRegulatory Affairs Certification (RAC), degree in life sciences or related fieldQuality Assurance certifications (e.g., CQE), degree in engineering or sciences
Work EnvironmentCollaborates with regulatory agencies, prepares submissions, reviews complianceMonitors product quality, audits, develops quality systems
Employer & Industry UsagePharmaceuticals, biotech, medical devicesManufacturing, pharmaceuticals, medical devices
Search & Comparison IntentOften compared for compliance roles in regulated industriesCompared for quality compliance roles in similar sectors

Remote Regulatory Affairs focuses on ensuring products meet regulatory standards and preparing submissions for approval, while Remote Quality Assurance emphasizes maintaining product quality through audits and process improvements. Both roles are essential in regulated industries and often overlap in compliance and documentation tasks, but they serve distinct functions within the product lifecycle.

What cities are hiring for Remote Regulatory Affairs jobs?

Cities with the most Remote Regulatory Affairs job openings:

What are the most commonly searched types of Regulatory Affairs jobs?

The most popular types of Regulatory Affairs jobs are:

What states have the most Remote Regulatory Affairs jobs?

States with the most job openings for Remote Regulatory Affairs jobs include:

Infographic showing various Remote Regulatory Affairs job openings in the United States as of August 2026, with employment types broken down into 75% Full Time, and 25% Contract. Highlights an 100% Remote job distribution, with an average salary of $82,307 per year, or $39.6 per hour.

Regulatory Affairs Specialist

Scale Inc

Burbank, CA • Remote

Full-time

Medical, Dental, Vision, Life, PTO

Posted 24 days ago


Job description

About Scale

For the past 12 years, Scale Media has been building and scaling science-backed wellness brands. Our portfolio of brands, including Live Conscious, 1MD, and Essential Elements, has grown to 9 figures in revenue while operating profitably with no external funding.

Our team is made up of operators, marketers, and builders focused on products consumers actually trust. We're investing heavily in data and AI to sharpen how we develop products and scale brands.

We believe the best decisions come from data, curiosity, and continuous learning. We value high ownership, candid feedback, and thoughtful execution. As a fully remote company, we lead with clear communication, accountability, and trust, and we give people real room to grow and make an impact.

Scale Media has been recognized as one of Forbes' Best Startup Employers, a Great Place to Work, an Inc. Best Workplace, and an Inc. 5000 company.

If you take ownership, think for yourself, and like solving hard problems alongside people who do the same, you'll fit right in.
About The Role

We're looking for a Regulatory Affairs Specialist to support compliance across our dietary supplement product lines. Reporting to the Regulatory Affairs Manager, you'll help ensure our labels, claims, and promotional materials meet FDA and FTC requirements — reviewing and interpreting regulatory standards, keeping documentation organized, and flagging risk before it reaches the market.

This is a hands-on, detail-driven role for someone who already knows their way around the dietary supplement space. You understand that claims have to be substantiated — that we can't just say things — and that supplements operate under real regulatory constraints. You'll work closely with Marketing, R&D, Product Development, and Quality as part of a small, high-trust regulatory team, with room to deepen your expertise over time.

What You'll DoClaims & Promotional Review
  • Review and approve promotional materials — commercial scripts, social media content, email, and marketplace listings — for compliance with FDA and FTC standards.
  • Apply structure/function and advertising requirements to flag risky language and recommend compliant alternatives.
  • Help ensure product claims are properly supported before they go live.
Substantiation Support
  • Support the claims substantiation process by reviewing and organizing supporting evidence and maintaining substantiation records.
  • Understand and apply the "competent and reliable scientific evidence" standard to assess whether a claim is adequately backed.
Labeling, SOPs & Compliance
  • Review supplement labels to ensure packaging and ingredient disclosures meet applicable requirements.
  • Assist in developing and maintaining regulatory SOPs, processes, and internal guidance.
  • Conduct or assist with Serious Adverse Event Reporting (SAER) investigations and documentation.
Monitoring & Cross-Functional Partnership
  • Monitor evolving FDA, FTC, and NAD developments — including warning letters and relevant industry litigation — and translate them into practical takeaways for the business.
  • Prepare and present industry updates at recurring team meetings (e.g., a monthly regulatory round-up), keeping cross-functional partners aware of what's happening and why it matters.
  • Partner with Marketing, R&D, Product Development, and Quality to provide practical regulatory guidance throughout the product lifecycle.
  • Manage the company’s trademark program: conduct initial trademark searches, maintain records, and coordinate with legal counsel for USPTO submissions.
Who You Are

You care about getting the details right, and you understand that good compliance protects the brand and the customer. You're a partner to the business, not a gatekeeper.

  • Detail-Oriented: You care about the details — because you know they add up to better, more trustworthy outcomes.
  • Clear Communicator: You express ideas clearly and make regulatory concepts easy to understand for non-regulatory teammates.
  • Organized & Deadline-Driven: You keep meticulous records and juggle competing priorities with ease, knowing that timely, well-organized documentation often gates product release.
  • Proactive: You anticipate needs, take ownership, and ask for support when needed.
  • Empowered Collaborator: You work across teams with trust and respect, and move projects forward through collective effort.
What You'll Need
  • 2–3 years of regulatory affairs experience in dietary supplements — this is our top priority. Not a first regulatory job, but not a senior-level tenure either.
  • A working understanding that product claims must be substantiated and that supplements operate under FDA and FTC regulation.
  • Experience reviewing labels and/or promotional materials for compliance.
  • Familiarity with DSHEA, 21 CFR Part 111, and structure/function claim basics.
  • Bachelor's degree in a life science, food science, or related field.
Preferred
  • Exposure to adjacent categories — cosmetics (MoCRA) or food/beverage — is a plus, though dietary supplement experience matters most.
  • DTC or eCommerce experience, including online marketplace (e.g., Amazon) compliance.
  • Comfort with quality or product documentation basics — reviewing specifications or Certificates of Analysis (COAs) and meeting the documentation timelines that gate product release.
  • Experience assisting with SOP development or regulatory process improvement.
  • Prior experience working within AI systems (Claude, Notion AI, etc.).

What We Offer

  • Salary: $75,000- $85,000
  • Medical, Dental, Vision, and Life Insurance
  • Fully remote, full-time position
  • Monthly work-from-home stipend
  • Generous paid time off program
  • Discounted products
  • An amazing team to work alongside

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