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Remote Regulatory Affairs Jobs (NOW HIRING)

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 ...

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 ...

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 ...

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 ...

Cardinal Health

This is a remote position, and the ideal candidate is located near Mansfield, MA or Waukegan, IL. Job Summary The Sr Regulatory Affairs Specialist will support the Medical Solutions Regulatory ...

Dentsply Sirona, Inc

Regulatory Affairs Manager

This position can be a remote working arrangement. Candidates must be located in the US, ideally in ... Manages day to day activities for less senior Regulatory Affairs professionals, including but not ...

Dentsply Sirona, Inc

Regulatory Affairs Manager

This position can be a remote working arrangement. Candidates must be located in the US, ideally in ... Manages day to day activities for less senior Regulatory Affairs professionals, including but not ...

Dentsply Sirona, Inc

Regulatory Affairs Manager

York, PA · On-site +1

This position can be a remote working arrangement. Candidates must be located in the US, ideally in ... Manages day to day activities for less senior Regulatory Affairs professionals, including but not ...

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 information

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How much do remote regulatory affairs jobs pay per hour?

As of Jul 16, 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 are the key skills and qualifications needed to thrive as a Remote Regulatory Affairs professional, and why are they important?

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.

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 are 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.

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.
More about Remote Regulatory Affairs jobs
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:
What job categories do people searching Remote Regulatory Affairs jobs look for? The top searched job categories for Remote Regulatory Affairs jobs are:
Remote Regulatory Affairs jobs near you
Infographic showing various Remote Regulatory Affairs job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 76% Full Time, 20% Part Time, 1% Temporary, and 2% Contract. Highlights an 79% Physical, 2% Hybrid, and 19% Remote job distribution, with an average salary of $82,307 per year, or $39.6 per hour.

Remote Regulatory Affairs contractor

Globalchannelmanagement

Atlanta, GA • Remote

$99 - $100/hr

Full-time

Posted 19 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