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Regulatory Affairs Jobs in Decatur, GA (NOW HIRING)

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 health insurance company built around a full stack technology platform and a relentless focus on ...

Analyst, Regulatory Affairs

Atlanta, GA · On-site

$28.30 - $37.15/hr

We're hiring a Analyst, Regulatory Affairs to join our Regulatory Affairs team. Oscar is the first health insurance company built around a full stack technology platform and a relentless focus on ...

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 health insurance company built around a full stack technology platform and a relentless focus on ...

Bachelor's degree in Regulatory Affairs, Life Sciences, Engineering, or a related field required Language: * English * Mandarin Preferred Professional Experience: * 2-3 years of regulatory affairs ...

Bachelor's degree in Regulatory Affairs, Life Sciences, Engineering, or a related field required Language: * English * Mandarin Preferred Professional Experience: * 2-3 years of regulatory affairs ...

Bachelor's degree in Regulatory Affairs, Life Sciences, Engineering, or a related field required Language: * English * Mandarin Preferred Professional Experience: * 2-3 years of regulatory affairs ...

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Regulatory Affairs information

See Decatur, GA salary details

$18

$38

$61

How much do regulatory affairs jobs pay per hour?

As of Jul 26, 2026, the average hourly pay for 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 Is Regulatory Affairs?

Regulatory affairs employees focus on meeting local, national, and international requirements for products. These jobs are particularly common in food, cosmetics, and companies that produce medicine or medical devices. With a position in regulatory affairs, you may be asked to ensure a medicine meets all safety regulations, prepare documents for submission to regulators, monitor translators to ensure the accurate translation of materials as needed, and ensure that records and reports are submitted in line with inspection standards. Regulatory affairs employees also provide support for currently-marketed products and may work with engineering drawings, technical files, or design history files to note required changes.

What are some typical challenges faced by professionals in Regulatory Affairs, and how can they be managed?

Regulatory Affairs professionals often navigate complex and ever-changing regulations across different regions, which can be challenging when managing multiple submissions or product lines. Staying up-to-date with regulatory updates and effectively communicating requirements to cross-functional teams is essential. Building strong relationships with regulatory agencies and leveraging robust internal processes can help streamline submissions and respond quickly to compliance issues. Proactive planning and regular professional development are key strategies for managing these challenges successfully.

What are the key skills and qualifications needed to thrive as a Regulatory Affairs professional, and why are they important?

To thrive as a Regulatory Affairs professional, you need a strong understanding of regulatory guidelines, compliance standards, and scientific or technical documentation, often supported by a degree in life sciences, pharmacy, or a related field. Familiarity with regulatory submission systems, document management tools, and certifications like RAC (Regulatory Affairs Certification) are commonly required. Excellent attention to detail, project management, and effective communication skills help professionals navigate complex regulations and collaborate with cross-functional teams. These competencies ensure timely product approvals, minimize compliance risks, and facilitate successful market access for products.

What are Regulatory Affairs?

Regulatory Affairs is a field focused on ensuring that companies comply with all of the regulations and laws pertaining to their business, particularly in industries such as pharmaceuticals, biotechnology, medical devices, and food. Professionals in Regulatory Affairs help guide products through the approval process by preparing and submitting required documentation to regulatory agencies like the FDA or EMA. They also monitor changes in regulations, advise on compliance strategies, and help organizations maintain market access for their products. This role is crucial for minimizing legal risks and ensuring the safety and efficacy of products.

What is the difference between Regulatory Affairs vs Quality Assurance?

AspectRegulatory AffairsQuality Assurance
Primary FocusEnsuring compliance with regulations and submitting documentation to authoritiesMaintaining product quality and implementing quality systems
Required CredentialsDegree in life sciences, regulatory certifications often preferredDegree in sciences or engineering, quality management certifications
Work EnvironmentRegulatory agencies, corporate compliance teamsManufacturing plants, quality departments
Industry UsagePharmaceuticals, biotech, medical devicesPharmaceuticals, manufacturing, medical devices

While Regulatory Affairs focuses on navigating regulatory requirements and submissions, Quality Assurance emphasizes maintaining product quality standards. Both roles are essential in ensuring products meet industry and legal standards, often collaborating closely within regulated industries.

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 Regulatory Affairs jobs in Decatur, GA look for? The top searched job categories for Regulatory Affairs jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Regulatory Affairs jobs? Cities near Decatur, GA with the most Regulatory Affairs job openings:
Infographic showing various Regulatory Affairs job openings in Decatur, GA as of July 2026, with employment types broken down into 92% Full Time, 6% Part Time, and 2% Contract. Highlights an 85% In-person, and 15% Remote job distribution, with an average salary of $80,359 per year, or $38.6 per hour.
Analyst, Regulatory Affairs

Analyst, Regulatory Affairs

Oscar Health

Atlanta, GA • Remote

$28.30 - $37.15/hr

Other

Medical, PTO

Posted 9 days ago


Oscar Health rating

6.9

Company rating: 6.9 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

247th of 298 rated insurance


Job description

Hi, we're Oscar. We're hiring a Analyst, Regulatory Affairs to join our Regulatory Affairs team.

Oscar is the first health insurance company built around a full stack technology platform and a relentless focus on serving our members. We started Oscar in 2012 to create the kind of health insurance company we would want for ourselves-one that behaves like a doctor in the family.

About the role:

The Analyst, Regulatory Affairs is a contributor and navigator who coordinates Regulatory Affairs work within the Evidence of Coverage team. You will coordinate large-scale, workgroups and contributes to annual QHP filings. You will support the Regulatory Affairs Evidence of Coverage team by serving as a resource on Oscar processes and identify risks to escalate in partnership with their manager.

You will report into the Regulatory Manager.

Work Location: This is a remote position, open to candidates who reside in: Atlanta, GA. You will be fully remote; however, our approach to work may adapt over time. Future models could potentially involve a hybrid presence at the hub office associated with your metro area. #LI-Remote

Pay Transparency: The base pay for this role is: $28.30 - $37.15 per hour. You are also eligible for employee benefits and monthly vacation accrual at a rate of 15 days per year.

Responsibilities:

  • Support annual QHP filings by ensuring the quality and timeliness of annual filing inputs through initial submission and regulator facing negotiation periods
  • Resolve low risk state objections
  • Project manages and implements the internal tracking and monitoring of Regulatory Affairs team deliverables related to our Legislative processes.
  • Coordinate internal working groups by scheduling meetings, intaking requests and ensuring the appropriate people are in the room
  • Prepare agendas, track action items, and follow-ups to ensure timely completion.
  • Maintain comprehensive documentation of regulatory objections, statespecific requirements, and reasons for deviations from standard policy.
  • Escalate issues or delays to leadership
  • Compliance with all applicable laws and regulations.
  • Other duties as assigned.

Requirements:

  • A bachelor's degree in a legal, healthcare-related or humanities field, or 4 years commensurate experience.
  • 2+ years of experience in health insurance customer service, claims, appeals, or Regulatory team
  • Strong attention to detail with the ability to manage complex documentation.

Bonus points:

  • Familiarity with health insurance operations
  • Experience with the individual market health insurance plans
  • Experience working with attorneys and internal stakeholders.
  • Proficiency in MS Office and Google Tools.

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