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Fda Inspector Jobs in Atlanta, GA (NOW HIRING)

CorDx

Regulatory Affairs Specialist

Alpharetta, GA · On-site

  • Medical

  • Retirement

  • PTO

Ensure product compliance with FDA regulations, ISO 13485, and applicable international standards ... Support the preparation for regulatory agency meetings, audits, and inspections Requirements ...

CorDx

Regulatory Affairs Manager (Atlanta)

Atlanta, GA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Ensure product compliance with FDA regulations, ISO 13485, and applicable international standards ... Support the preparation for regulatory agency meetings, audits, and inspections. * Collaborate with ...

CorDx

Regulatory Affairs Manager (Atlanta)

Atlanta, GA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Ensure product compliance with FDA regulations, ISO 13485, and applicable international standards ... Support the preparation for regulatory agency meetings, audits, and inspections. * Collaborate with ...

CorDx

Regulatory Affairs Manager (Atlanta)

Atlanta, GA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Ensure product compliance with FDA regulations, ISO 13485, and applicable international standards ... Support the preparation for regulatory agency meetings, audits, and inspections. * Collaborate with ...

tbc

Donor Services Trainer (Decatur)

Decatur, GA · On-site

Training is performed in accordance to departmental procedures, processes, policies along with FDA ... Ensures staff training manuals are inspection/audit ready * Updates departmental JDTRs ( Training ...

Workforce Consultants

Factory Facility Supervisor

White, GA · On-site

$75K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Maintain high sanitation and workplace safety standards in compliance with SQF,HACCP,FDA requirements and OSHA regulations to ensure readiness for third-party audits and regulatory inspections.

Artivion

Sr. Clinical Data Manager

Kennesaw, GA · On-site

Ensure data integrity and compliance with GCP, FDA, MDR/IVDR, and other applicable regulatory ... Support audit readiness and participate in regulatory inspections when required. * Mentor junior ...

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Showing results 41-60

All JobsFda Inspector JobsFda Inspector Jobs in Atlanta, GA

Fda Inspector information

See Atlanta, GA salary details

$23.6K

$52.8K

$95.2K

How much do fda inspector jobs pay per year?

As of Aug 17, 2026, the average yearly pay for fda inspector in Atlanta, GA is $52,833.00, according to ZipRecruiter salary data. Most workers in this role earn between $37,000.00 and $61,100.00 per year, depending on experience, location, and employer.

What types of facilities or products do FDA inspectors review, and what does a typical inspection process involve?

FDA Inspectors routinely examine a variety of facilities, such as food processing plants, pharmaceutical manufacturers, medical device companies, and cosmetic production sites, to ensure compliance with federal safety and quality regulations. A typical inspection involves reviewing operational procedures, examining production environments, sampling products, and interviewing staff to identify potential violations or risks. Inspectors often work onsite, sometimes with travel required to cover multiple locations within their region, and collaborate closely with facility management to explain findings and recommend corrective actions. This role offers the opportunity to make a significant impact on public health and provides clear advancement pathways into specialized inspection or supervisory roles within regulatory agencies.

What skills and qualifications are needed to be an FDA inspector?

To thrive as an FDA Inspector, you need a solid background in science or public health, attention to detail, and thorough knowledge of regulatory standards, often supported by a relevant degree. Familiarity with inspection protocols, laboratory testing equipment, and digital reporting systems is commonly required, along with potential USDA or FDA certifications. Strong analytical thinking, effective communication, and integrity are important soft skills for this role. These competencies ensure accurate inspections, compliance with safety regulations, and clear reporting essential to public health and organizational accountability.

How do you become an FDA inspector?

To become an FDA inspector, candidates typically need a bachelor's degree in a relevant field such as biology, chemistry, or food science, along with experience in food safety, pharmaceuticals, or related areas. They must pass the FDA's specialized training program and often require a background check and security clearance; some positions may also require state licensure or certifications. Strong attention to detail, knowledge of regulatory standards, and good communication skills are essential for the role.

What does an FDA inspector do?

An FDA Inspector is responsible for ensuring that companies comply with federal regulations related to food, drugs, medical devices, and other products overseen by the U.S. Food and Drug Administration. They conduct inspections, review records, collect samples, and assess manufacturing practices to ensure public health and safety. Inspectors may also investigate complaints, issue compliance notices, and recommend enforcement actions if violations are found.

What are popular job titles related to Fda Inspector jobs in Atlanta, GA?

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What job categories do people searching Fda Inspector jobs in Atlanta, GA look for?

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What cities near Atlanta, GA are hiring for Fda Inspector jobs?

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Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in Atlanta, GA as of August 2026, with employment types broken down into 74% Full Time, 12% Part Time, 13% Contract, and 1% Nights. Highlights an 98% Physical, and 2% Remote job distribution, with an average salary of $54,508 per year, or $26.2 per hour.

Regulatory Affairs Specialist

CorDx

Alpharetta, GA • On-site

Full-time

Medical, Retirement, PTO

Re-posted 2 days ago

Job description

About Us

CorDx, a multi-national biotech organization, focused on pushing the limits of innovation and supply in global health. With over 2000 employees across the world serving millions of users in over 100 countries, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious diseases such as COVID-19, pregnancy, drug abuse, biomarkers, and more. CorDx is at the cutting edge of technology, artificial intelligence, and data science with the goal of delivering diagnostic solutions to some of the most critical questions in healthcare.

Position Summary

The Regulatory Affairs Specialist will support the preparation, review, and submission of regulatory documentation for medical device/IVDs products, ensuring compliance with applicable regulatory requirements including FDA, ISO 13485, and other global standards. This position focus on submitted documents preparing, helping to secure timely product approvals and regulatory clearances.

Key Responsibilities

  • Prepare, review, and coordinate the submission of regulatory documents including 510(k), technical files, and other filings to regulatory agencies
  • Ensure product compliance with FDA regulations, ISO 13485, and applicable international standards
  • Working on analytical performance test with product development teams to draft documentation.
  • Perform regulatory assessments for product changes and propose appropriate regulatory pathways
  • Maintain documentation and records of all regulatory submissions and correspondence
  • Support the preparation for regulatory agency meetings, audits, and inspections

Requirements

Education:

  • 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 experience within the medical device or IVD industry
  • Working knowledge of 510(k) submissions and regulatory documentation processes
  • Experience interacting with FDA and other regulatory agencies preferred

Skills & Competencies:

  • Solid understanding of FDA regulations and Guidance. (510k, PMA, De novo)
  • Strong organizational and project management skills with the ability to manage multiple projects and priorities
  • Excellent communication, problem-solving, and attention to detail
  • Ability to work collaboratively in cross-functional teams and manage document workflows

Benefits

  • Comprehensive medical insurance.
  • 401(k) plan with company contributions.
  • Flexible paid time off (PTO) policy.

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