ZipRecruiter

Log In

1

Regulatory Affairs Jobs in Decatur, GA (NOW HIRING)

micro1 AI

Compliance Officers

Atlanta, GA · Remote

$50 - $70/hr

Regulatory Affairs Specialist Role Type: Contractor Location: Remote micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project focused on AI innovation in regulatory ...

micro1 AI

Compliance Officers

Sandy Springs, GA · Remote

$50 - $70/hr

Regulatory Affairs Specialist Role Type: Contractor Location: Remote micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project focused on AI innovation in regulatory ...

micro1 AI

Compliance Officers

South Fulton, GA · Remote

$50 - $70/hr

Regulatory Affairs Specialist Role Type: Contractor Location: Remote micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project focused on AI innovation in regulatory ...

UCB

Head of REMS US, Atlanta, GA

Atlanta, GA · On-site

$184K - $242K/yr

Who you'll work with You'll collaborate with internal teams involved in and impacted by REMS, including Regulatory Affairs, Medical Affairs, Pharmacovigilance, Patient Safety, Quality, Patient ...

UCB

Head of REMS US, Atlanta, GA

Atlanta, GA · On-site

$184K - $242K/yr

Whoyou'llwork with You'llcollaborate with internal teams involved in andimpactedby REMS, including Regulatory Affairs, Medical Affairs, Pharmacovigilance, Patient Safety, Quality, Patient Services ...

UCB

GRA Device Lead, Atlanta, GA

Atlanta, GA · On-site

$148K - $195K/yr

About the role The Global Regulatory Affairs Devices Lead supports regulatory strategy and submissions for marketed and development medical devices and combination products within Neurology ...

UCB

GRA Device Lead, Atlanta, GA

Atlanta, GA · Hybrid

$148K - $195K/yr

About the role The Global Regulatory Affairs Devices Lead supports regulatory strategy and submissions for marketed and development medical devices and combination products within Neurology ...

Quickchek

Regulatory & Licensing Paralegal

Alpharetta, GA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Mountain Express Oil Company is seeking a corporate regulatory affairs paralegal to support our growing legal team. The ideal candidate will be experienced at filing corporate licenses at the state ...

Deloitte

Regulatory Reporting Manager

Atlanta, GA · On-site

As an experienced Regulatory Reporting Manager you will have the ability to share new ideas and collaborate on projects as a consultant without the extensive demands of travel. If so, consider an ...

LivaNova

Regulatory & Clinical Specialist

Atlanta, GA · Remote

$85K - $95K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... regulatory 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 ...

LivaNova

Regulatory & Clinical Specialist

Hapeville, GA · On-site

$85K - $95K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... regulatory 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 ...

LivaNova

Regulatory & Clinical Specialist

Atlanta, GA · On-site

$85K - $95K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... regulatory 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 ...

previous pagenext page

Showing results 21-40

All JobsRegulatory Affairs JobsRegulatory Affairs Jobs in Decatur, GA

Regulatory Affairs information

See Decatur, GA salary details

$18

$38

$61

How much do regulatory affairs jobs pay per hour?

As of Aug 17, 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 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.

How much do regulatory affairs jobs pay in the US?

Regulatory affairs professionals in the US typically earn a median annual salary of around $100,000, with entry-level positions starting at approximately $70,000 and experienced roles reaching over $130,000. Salaries vary based on experience, industry, location, and certifications such as RAC, and the role often requires knowledge of regulatory guidelines and compliance processes.

What do regulatory affairs jobs do?

Regulatory affairs professionals ensure that companies comply with government regulations and industry standards for product development, approval, and marketing. They prepare and submit documentation to regulatory agencies, monitor changes in regulations, and coordinate with cross-functional teams to ensure products meet safety and efficacy requirements throughout their lifecycle.
More about Regulatory Affairs jobs

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 are popular job titles related to Regulatory Affairs jobs in Decatur, GA?

For Regulatory Affairs jobs in Decatur, GA, the most frequently searched job titles 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:

Regulatory Affairs jobs near you
Infographic showing various Regulatory Affairs job openings in Decatur, GA as of August 2026, with employment types broken down into 93% Full Time, 5% 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.

Regulatory Affairs Specialist (North America)

Alimentiv

Atlanta, GA • Remote

Full-time

Re-posted 6 days ago

Job description

Responsible for the day-to-day activities and delivery of Global Regulatory Affairs support services. Role will include management of clinical trial applications to Competent Authorities, Ethics Committees and Regulatory Agencies, and the research, review and reporting on applicable global regulations and requirements. Develop stakeholder tools, process/document regulatory risk assessments, and provide support, expertise and represent the unit with other functional units, sponsors, researchers and/or regulatory authorities.  Ensure high quality, timely service delivery processes are maintained in accordance with corporate, industry and regulatory standards and guidelines.  May be required to coach peers and/or provide input for staff performance reviews. 
Unit Management
  • Coordinate the day to day delivery of regulatory services and processes, including compilation of regulatory filings/submissions/revisions for projects, third party vendors and clinical sites.
  • Conduct or assist with regulatory and/or safety reviews, create regulatory-related tools, educational/training materials, and remain current on all aspects of clinical research regulatory requirements and industry best practices, communicating changes to project leaders in a timely manner.
Client Services
  • As the corporate subject specialist in regulatory affairs, provide regulatory, ethics and/or pharmacovigilance guidance and support to project stakeholders.
  • Represent the unit at project meetings, assisting with project education/regulatory tool development, at regulatory reviews and audits, with clients ensuring expectations are managed and met, with regulatory, ethics and government representatives and, when appropriate, respond to regulatory queries on behalf of the client.
Regulatory Strategy Development
  • Identify changes in clinical research regulatory requirements and industry best practices and recommend, implement, and maintain corporate regulatory strategies, working with other experts (safety, quality assurance) when appropriate, to meet or exceed compliance requirements of evolving regulatory initiatives.
  • Participate in specialized conferences/meetings to increase knowledge as needed.
Project Support
  • Regularly respond to registration requests and work with project teams to identify regulatory requirements.
  • Assist in the preparation of regulatory submissions and support summaries.
  • Ensure project/clinical site files and documents are developed, maintained, revised, archived and/or destroyed in accordance with project and regulatory requirements and that all project stakeholders are fully informed and trained on all applicable regulatory requirements.
Qualifications
  • Applicants should have a minimum of an undergraduate degree and 4-6 years of relevant experience in Clinical Research/Regulatory Affairs.
  • The successful candidate will possess strong knowledge of LATAM clinical trial regulations.
  • Fluency in English and Spanish (written and verbal) required.
Working Conditions
  • Home-based
  • *Accommodations for job applicants with disabilities are available upon request.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
apply for this job

Apply