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Fda Biologist Jobs in Georgia (NOW HIRING)

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Biologics Procurement Specialist

Norcross, GA · On-site

$70 - $100/hr

Overview We are looking for a Biologics Procurement Specialist manages the Reagent Donor Program ... Understands FDA and ISO standards applicable to the department and consequences of nonconformance.

ADMA Biologics

Center Training Coordinator

Conyers, GA · On-site

$60 - $75/hr

ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products ... FDA regulations and company policies governing sales and marketing activities. This includes ...

MiMedx Group

Metrology Technician

Marietta, GA · On-site

$56K - $70K/yr

... Biology, Chemistry, etc.) and two (2) years of relevant work experience working in the medical device field or in a Metrology role within an FDA regulated cGMP environment; or a combination of ...

MIMEDX

Metrology Technician

Marietta, GA · On-site

$56K - $70K/yr

... Biology, Chemistry, etc.) and two (2) years of relevant work experience working in the medical device field or in a Metrology role within an FDA regulated cGMP environment; or a combination of ...

MIMEDX Careers

Metrology Technician

Marietta, GA · On-site

$56 - $70/hr

... Biology, Chemistry, etc.) and two (2) years of relevant work experience working in the medical device field or in a Metrology role within an FDA regulated cGMP environment; or a combination of ...

Mimedx

Metrology Technician

Marietta, GA · On-site

$56 - $70/hr

... Biology, Chemistry, etc.) and two (2) years of relevant work experience working in the medical device field or in a Metrology role within an FDA regulated cGMP environment; or a combination of ...

Carlyle's Catering

Be Seen First

Quality Assurance (QA) Manager / Food Safety Manager

Atlanta, GA · On-site

$55K - $65K/yr

This position ensures compliance with all applicable FDA, USDA, Georgia Department of Agriculture ... Biology * Culinary Science * Related Field OR Equivalent combination of education and food ...

Kuros Biosciences, Inc.

Operator

Alpharetta, GA · On-site

$17 - $22.50/hr

... and FDA regulations. This role is critical to ensuring product quality, traceability, and ... Education: * Bachelor's degree in Biology, Chemistry Engineering, Biology, or related field ...

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All JobsFda Biologist JobsFda Biologist Jobs in Georgia

Fda Biologist information

See Georgia salary details

$31.2K

$75.5K

$116.5K

How much do fda biologist jobs pay per year?

As of Sep 6, 2026, the average yearly pay for fda biologist in Georgia is $75,491.00, according to ZipRecruiter salary data. Most workers in this role earn between $50,200.00 and $102,200.00 per year, depending on experience, location, and employer.

What is an FDA biologist?

An FDA Biologist is a scientist who evaluates biological products, research data, and laboratory studies to ensure public health and safety. They work on regulatory reviews, inspections, and policy development related to vaccines, gene therapy, blood products, and other biologics. Their role helps ensure compliance with federal regulations and supports scientific advancements in healthcare.

What are the typical daily responsibilities of an FDA biologist?

An FDA Biologist’s daily tasks often include reviewing scientific data, conducting laboratory experiments, and preparing reports on biological product submissions. You may assess the safety and efficacy of products such as vaccines or medical devices, ensuring compliance with regulatory standards. Collaboration with interdisciplinary teams—including chemists, statisticians, and regulatory affairs specialists—is common to address scientific questions and support regulatory decision-making. The role also involves staying updated on scientific advancements and regulatory changes relevant to the field. This dynamic environment provides opportunities to contribute to public health while developing specialized expertise.

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

To thrive as an FDA Biologist, you need a degree in biology or a related scientific field, strong analytical and laboratory skills, and a solid understanding of regulatory requirements. Familiarity with laboratory instruments, scientific data analysis tools, and regulatory databases such as GLP (Good Laboratory Practice) systems is important. Attention to detail, effective communication, and strong problem-solving abilities are valuable soft skills in this role. These competencies are crucial for accurately evaluating biological data, ensuring regulatory compliance, and collaborating effectively within multidisciplinary teams at the FDA.

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

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

What are popular job titles related to Fda Biologist jobs in Georgia?

For Fda Biologist jobs in Georgia, the most frequently searched job titles are:

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

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

Fda Biologist jobs near you
Infographic showing various Fda Biologist job openings in Georgia as of August 2026, with employment types broken down into 81% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $75,491 per year, or $36.3 per hour.

Senior Regulatory Associate -- Drugs & Biologics

The FDA Law Solution

Atlanta, GA • On-site

$100 - $130/hr

Other

Posted 5 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 — Drugs & Biologics

Location: Atlanta, GA (On‑Site) • Full‑Time • 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 GLP‑1 compounding and USP requirements.
  • Manage inspection readiness and draft responses to FDA 483s.
  • Draft high‑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 post‑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 high‑priority client matters independently and efficiently.
  • Participate in team meetings to align legal strategy with business goals.
  • Communicate complex regulatory concepts to non‑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.
  • Expert‑level legal writing, issue spotting, and regulatory analysis skills.
  • Strong scientific literacy for engagement with technical and clinical data.
  • Experience with GLP‑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 write‑offs (preferred).
Location and Working Conditions

Position is based onsite at our Atlanta, GA office. Standard business hours apply with occasional deadline‑driven intensity. Collaborative environment requiring frequent face‑to‑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 solution‑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 cutting‑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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