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Remote Regulatory Intelligence Jobs in Georgia (NOW HIRING)

Oscar Health

Analyst, Regulatory Affairs

Atlanta, GA · Remote

$28.30 - $37.15/hr

This is a remote position, open to candidates who reside in: Atlanta, GA. You will be fully remote ... Artificial Intelligence (AI): Our AI Guidelines outline the acceptable use of artificial ...

Corpay

Vice President of Financial Intelligence Unit

Atlanta, GA · Remote

$121K - $162K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... regulatory reporting, typology intelligence, quality assurance, and risk reporting to the Chief ... Assigned workspace in your local officeor remote work support * Company-issued equipment ...

Honeywell

Lead Account Manager - REMOTE

Atlanta, GA · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Monitor industry trends, regulatory changes, and competitive landscape to proactively identify ... intelligence layer. By combining the deep domain expertise of our more than 50,000 employees with ...

Honeywell

Lead Account Manager - REMOTE

Atlanta, GA · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Strong business acumen and understanding of regulatory and operational challenges in Healthcare and ... intelligence layer. By combining the deep domain expertise of our more than 50,000 employees with ...

Honeywell

Lead Account Manager - REMOTE

Atlanta, GA · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Strong business acumen and understanding of regulatory and operational challenges in Healthcare and ... intelligence layer. By combining the deep domain expertise of our more than 50,000 employees with ...

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All JobsRegulatory Intelligence JobsRemote Regulatory Intelligence JobsRemote Regulatory Intelligence Jobs in Georgia

Remote Regulatory Intelligence information

What is the difference between Remote Regulatory Intelligence vs Regulatory Affairs Specialist?

AspectRemote Regulatory IntelligenceRegulatory Affairs Specialist
CredentialsTypically requires degrees in life sciences, certifications in regulatory affairs or intelligenceRequires degrees in life sciences, certifications like RAC or RAPS
Work EnvironmentPrimarily remote, focused on research and analysisOften office-based or hybrid, involved in compliance and submission processes
Industry UsageUsed in pharmaceutical, biotech, and medical device sectors for monitoring regulationsInvolved in preparing and submitting regulatory documents to authorities

Remote Regulatory Intelligence focuses on gathering and analyzing regulatory information remotely, while Regulatory Affairs Specialists handle compliance, submissions, and communication with authorities. Both roles require regulatory knowledge but differ in daily tasks and work settings.

What are the most commonly searched types of Regulatory Intelligence jobs in Georgia?

The most popular types of Regulatory Intelligence jobs in Georgia are:

What are popular job titles related to Remote Regulatory Intelligence jobs in Georgia?

For Remote Regulatory Intelligence jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Remote Regulatory Intelligence jobs in Georgia look for?

The top searched job categories for Remote Regulatory Intelligence jobs in Georgia are:

What cities in Georgia are hiring for Remote Regulatory Intelligence jobs?

Cities in Georgia with the most Remote Regulatory Intelligence job openings:

Remote Regulatory Intelligence jobs near you
Infographic showing various Remote Regulatory Intelligence job openings in Georgia as of August 2026, with employment types broken down into 67% Full Time, and 33% Part Time. Highlights an 100% Remote job distribution.

Remote Regulatory Affairs contractor

Globalchannelmanagement

Atlanta, GA • Remote

$99 - $100/hr

Full-time

Re-posted 23 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