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Remote Regulatory Affairs Jobs in Decatur, GA (NOW HIRING)

... affairs or a Ph.D. with at least 3 years of experience Location & Travel Requirements ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

VP, State Government Affairs

Atlanta, GA · On-site +1

$220K - $275K/yr

Anticipate evolving regulatory trends, influencing policy outcomes before they crystallize, and ... S. and are willing to consider remote candidates. #LI-Remote Working at PrizePicks: The typical ...

... Regulatory Affairs (ORA). The duties for this position is as follows: Work with end users and ... This is a remote position so the candidate can live anywhere in the USA. The position will require ...

Director - Product Security

Atlanta, GA · On-site +1

$224K - $234K/yr

Houston, TX is the ideal location for this role, but this is open to Remote opportunities for well ... Partner with R&D, Engineering, Quality, Regulatory Affairs, and Legal teams to embed security ...

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Remote Regulatory Affairs information

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How much do remote regulatory affairs jobs pay per hour?

As of Jun 16, 2026, the average hourly pay for remote regulatory affairs in Decatur, GA is $38.63, according to ZipRecruiter salary data. Most workers in this role earn between $30.96 and $45.77 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.
What are the most commonly searched types of Regulatory Affairs jobs in Decatur, GA? The most popular types of Regulatory Affairs jobs in Decatur, GA are:
What job categories do people searching Remote Regulatory Affairs jobs in Decatur, GA look for? The top searched job categories for Remote Regulatory Affairs jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Remote Regulatory Affairs jobs? Cities near Decatur, GA with the most Remote Regulatory Affairs job openings:
Manager, Clinical Science, Medical Affairs

Manager, Clinical Science, Medical Affairs

Danaher

Atlanta, GA • On-site, Remote

$150K - $170K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted yesterday


Danaher rating

7.5

Company rating: 7.5 out of 10

Based on 27 frontline employees who took The Breakroom Quiz


Job description

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Integrated DNA Technologies (IDT), one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.

You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.

Our team at Integrated DNA Technologies (IDT), is united by a commitment to collaboration and scientific excellence, building on a strong foundation of innovation, expertise, and reliability. Guided by our vision to help researchers rapidly move from the lab to life-changing advances, we work closely with global partners to accelerate progress and genomics breakthroughs across fields like cancer, infectious disease, rare genetic disorders, and more. At IDT, you'll be part of a culture rooted in continuous learning and improvement-where your growth fuels our mission to accelerate the pace of genomics and helps shape a healthier, brighter future for all.

Learn about the Danaher Business System which makes everything possible.

The Manager, Clinical Science, Medical Affairs is a critical strategic role in driving sustainable business value ensuring the scientific credibility, regulatory compliance and clinical relevance of the organization's products. This role will serve as a trusted scientific partner to internal/external stakeholders-including healthcare professionals, crossfunctional teams, and external collaborators - directly influencing product adoption, appropriate use, and longterm market success.

This position reports to the Director, Global Regulatory Affairs, Product Lifecycle Quality and Compliance and is part of the global QA/RA function located in Coralville, IA and will be fully remote.

In this role, you will have the opportunity to:

  • Develop and execute medical strategy aligned with product lifecycle stages, diagnostic priorities, and overall business objectives, ensuring scientific integrity and compliance.
  • Serve as a scientific expert and liaison to healthcare professionals, key opinion leaders, and internal stakeholders to facilitate clinical education, evidence exchange, and trusted relationships associated with off-label inquiries, third-party validation services, health hazard assessments, etc.
  • Lead generation, interpretation, and communication of medical evidence, including clinical data, realworld evidence, and publications, to support appropriate product use and informed decisionmaking.
  • Ensure regulatory, ethical, and compliance adherence across all medical activities, mitigating risk and maintaining a clear separation between medical and promotional functions.
  • Provide strategic medical insights to crossfunctional teams (commercial, market access, R&D, regulatory) to inform product development, launch planning, and postmarketing strategies.

The essential requirements of the job include:

  • Bachelor's degree in Biostatistics, Life Science, Chemistry, Biochemistry or equivalent; MD or PhD preferred
  • 5-10 years experience in Medical Device/Pharma/IVD companies
  • Experience in next generation sequencing with proficient knowledge of medical terminology
  • With minimal supervision, demonstrate a high level of customer service skills, approachability, and sense of urgency with strong collaboration skills (communication, tone, messaging, execution, planning, ownership).

Travel, Motor Vehicle Record & Physical/Environment Requirements:

  • Ability to travel 10% domestically, and internationally

It would be a plus if you also possess previous experience in:

  • a Medical Affairs role, such as a Medical Science Liaison (MSL)
  • Novel Biomarker Assay Development

IDT, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.

At IDT we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for IDT can provide.

The annual salary range for this role is $150,000 - $170,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.

This job is also eligible for bonus/incentive pay.

We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.

Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.


For more information, visit www.danaher.com.


Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.


The U.S. EEO posters are available here.


For candidates who are based outside of New York City or who are applying for roles outside of New York City, for more information about conditions of any job offer please click here.


We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or applyassistance@danaher.com.


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About Danaher

Sourced by ZipRecruiter

We are a science and technology innovator committed to helping our customers solve complex challenges, and improving quality of life around the world. A global family of more than 20 operating companies, we drive meaningful innovation in some of today's most dynamic, growing industries.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Washington, DC, US

Year founded

1984