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Fda Scientist Jobs in Georgia (NOW HIRING)

Strong understanding of FDA, EUA, and other global regulatory requirements * Demonstrated technical and project leadership expertise * Good organization skills, detailed oriented mindset * Ability to ...

Clinical Affairs Scientist

Turin, GA ยท On-site +1

$105K - $197K/yr

We are searching for an experienced Clinical Affairs Scientist (CAS) to work within the medical ... Experience working with external partners and/or regulatory bodies including the FDA. * Knowledge ...

Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA 510(k)/PMA, CEIVDR) across multiple diagnostic modalities. * Act as a scientific and clinical ...

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Fda Scientist information

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$42.6K

$94K

$116.1K

How much do fda scientist jobs pay per year?

As of Sep 7, 2026, the average yearly pay for fda scientist in Georgia is $94,016.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,800.00 and $115,700.00 per year, depending on experience, location, and employer.

What is an FDA Scientist?

An FDA Scientist is a researcher or regulatory expert responsible for evaluating the safety, efficacy, and quality of pharmaceutical drugs, medical devices, biologics, and food products. They conduct laboratory research, review clinical trial data, and assess regulatory submissions to ensure compliance with federal laws and guidelines. FDA Scientists play a critical role in protecting public health by making science-based decisions on product approvals and safety standards.

What types of projects and responsibilities can I expect as an FDA Scientist?

As an FDA Scientist, you'll typically be involved in reviewing data from clinical trials, conducting laboratory research, evaluating the safety and efficacy of pharmaceuticals or medical devices, and preparing reports for regulatory submissions. You'll collaborate closely with multidisciplinary teams including chemists, statisticians, and regulatory specialists to ensure scientific rigor and adherence to federal standards. Some days may involve detailed data analysis, while others could require participating in cross-team meetings or interacting with external stakeholders. This dynamic environment offers opportunities to contribute to important public health decisions and develop specialized expertise over time.

What are the key skills and qualifications needed to thrive in the FDA Scientist position, and why are they important?

To thrive as an FDA Scientist, you need a solid background in biology, chemistry, pharmacology, or a related scientific field, typically supported by at least a bachelor's or advanced degree. Familiarity with regulatory submission systems, laboratory information management systems (LIMS), and relevant certifications such as Good Laboratory Practice (GLP) or Good Clinical Practice (GCP) is important. Strong analytical thinking, attention to detail, and effective communication skills help you excel when collaborating with colleagues and presenting findings. These abilities ensure accurate data review and regulatory compliance, which are crucial for advancing public health and safety.

How much do FDA scientists make?

FDA scientists typically earn between $70,000 and $130,000 annually, depending on experience, education, and location. Entry-level positions often start around $70,000, while experienced scientists with advanced degrees can earn higher salaries, especially in supervisory or specialized roles.

What are the most commonly searched types of Fda Scientist jobs in Georgia?

The most popular types of Fda Scientist jobs in Georgia are:

What job categories do people searching Fda Scientist jobs in Georgia look for?

The top searched job categories for Fda Scientist jobs in Georgia are:

What cities in Georgia are hiring for Fda Scientist jobs?

Cities in Georgia with the most Fda Scientist job openings:

Infographic showing various Fda Scientist job openings in Georgia as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $94,016 per year, or $45.2 per hour.

Senior Regulatory Associate -- Drugs & Biologics

The FDA Law Solution

Atlanta, GA โ€ข On-site

$100 - $125/hr

Other

Posted 6 days ago


Key responsibilities

  • Support strategy development for FDA, FTC, USDA, EPA, IND, NDA, and BLA programs.

  • Manage inspection readiness, draft responses to FDA 483s, and handle regulatory compliance documentation.

  • Coordinate with client departments and manage multiple high-priority client matters independently.


Job description

Senior Regulatory Associate โ€” Drugs & Biologics

Location: Atlanta, GA (Onโ€‘Site) โ€ข Fullโ€‘Time โ€ข Reports to: Founder & CEO

About the Company

The FDA Law Solution, LLC. is a premier legal advisory firm specializing in navigating the complex regulatory landscape of the Food and Drug Administration. Led by industry veteran Ricky C. Benjamin, the firm provides strategic counsel to life sciences and healthcare companies to ensure product compliance and successful market entry.

Responsibilities
  • Support strategy for FDA, FTC, USDA, EPA, IND, NDA, and BLA development and commercialization programs.
  • Execute rare disease regulatory strategies including orphan drug designations.
  • Provide technical counsel on GLPโ€‘1 compounding and USP requirements.
  • Manage inspection readiness and draft responses to FDA 483s.
  • Draft highโ€‘level regulatory analyses and strategic client guidance memos.
  • Manage promotional and labeling review for FDA and FTC compliance.
  • Facilitate PRC and MLR meetings with minimal senior oversight.
  • Monitor postโ€‘market compliance and adverse event reporting requirements.
  • Conduct regulatory due diligence for life science transactions and acquisitions.
  • Draft formal responses to FDA Warning Letters and enforcement actions.
  • Coordinate with client Regulatory Affairs, Quality, and Marketing departments.
  • Manage multiple highโ€‘priority client matters independently and efficiently.
  • Participate in team meetings to align legal strategy with business goals.
  • Communicate complex regulatory concepts to nonโ€‘legal client stakeholders.
  • Maintain professional relationships with FDA project managers and officials.
Qualifications
  • Juris Doctor (JD) degree and active bar membership in good standing.
  • 5+ years of FDA regulatory law experience.
  • Proven track record in submission strategies for FDA, FTC, USDA, EPA, IND, NDA, and BLA.
  • Expertโ€‘level legal writing, issue spotting, and regulatory analysis skills.
  • Strong scientific literacy for engagement with technical and clinical data.
  • Experience with GLPโ€‘1 compounding (503B) and USP 797/795 standards (preferred).
  • Technical proficiency with Veeva PromoMats for promotional review (preferred).
  • Experience securing orphan drug designations for rare diseases (preferred).
  • Familiarity with REMS programs and market exclusivity strategies (preferred).
  • History of high billable efficiency with minimal time writeโ€‘offs (preferred).
Location and Working Conditions

Position is based onsite at our Atlanta, GA office. Standard business hours apply with occasional deadlineโ€‘driven intensity. Collaborative environment requiring frequent faceโ€‘toโ€‘face engagement with the Founder. Occasional travel may be required for client site visits or inspections.

Compensation & Benefits

Competitive compensation and benefit package based on candidate's experience level.

Culture & Expectations
  • Demonstrate absolute accountability and ownership over client deliverables.
  • Maintain a solutionโ€‘oriented mindset when navigating complex regulatory barriers.
  • Exhibit professional resilience and reliability under tight agency deadlines.
  • Practice clear, respectful, and proactive communication with internal teams.
  • Align with the firm's dedication to precision and protective advocacy.
Growth & Development

This role offers a unique path to senior leadership through direct mentorship from the firm's Founder and CEO. It provides exposure to cuttingโ€‘edge specialty regulatory areas often unavailable in larger firm settings and encourages internal advancement for associates who demonstrate business savvy and commitment to expanding the firm's influence and client base.

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