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Fda Inspector Jobs in Atlanta, GA (NOW HIRING)

InspireMD

Field Clinical Specialist

Atlanta, GA · Remote

$75K - $81K/yr

Support FDA inspections and audits, ensuring that all regulatory and complaint handling documentation is in order and facilitating smooth interactions with regulatory authorities. Qualifications:

CenExel

Quality Assurance Coordinator

Decatur, GA · On-site

$53K - $55K/yr

Prepares for internal and external audits and FDA inspections. * Attends staff meetings. * Attends site initiation visits as needed. * Supports and ensures strictest adherence to best practices, FDA ...

Abbott

Manager, Quality Assurance

Atlanta, GA

Actively participate in FDA inspections and lead internal/corporate audits, notified body audits and applicable external certification audits including any post-audit responses. * Provide support for ...

Abbott

Manager, Quality Assurance

Atlanta, GA

Actively participate in FDA inspections and lead internal/corporate audits, notified body audits and applicable external certification audits including any post-audit responses. * Provide support for ...

Abbott

Senior Quality Engineer

Atlanta, GA · On-site

$78K - $156K/yr

Experience supporting FDA inspections and external audits. * Strong knowledge of FDA Quality System Regulation, ISO 13485, CAPA, complaints, risk management, and manufacturing quality systems. Apply ...

Abbott

Senior Quality Engineer

Atlanta, GA

$78K - $156K/yr

Experience supporting FDA inspections and external audits. * Strong knowledge of FDA Quality System Regulation, ISO 13485, CAPA, complaints, risk management, and manufacturing quality systems. Apply ...

Abbott

Manager, Quality Assurance

Atlanta, GA · On-site

Actively participate in FDA inspections and lead internal/corporate audits, notified body audits and applicable external certification audits including any post-audit responses. * Provide support for ...

Abbott

Senior Quality Engineer

Atlanta, GA

$78K - $156K/yr

Experience supporting FDA inspections and external audits. * Strong knowledge of FDA Quality System Regulation, ISO 13485, CAPA, complaints, risk management, and manufacturing quality systems. Apply ...

CorDx

Regulatory Affairs Specialist

Alpharetta, GA · On-site

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 Specialist

Alpharetta, GA · On-site

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

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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 Jul 21, 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.

How much do FDA drug investigators make?

FDA drug investigators typically earn a salary ranging from $70,000 to $120,000 annually, depending on experience, location, and level of responsibility. They often hold a bachelor's degree in a relevant field and may require specialized training or certifications related to regulatory compliance and inspection procedures.

What types of facilities or products do FDA Inspectors typically 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 are the key skills and qualifications needed to thrive in the Fda Inspector position, and why are they important?

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.

What type of inspector gets paid the most?

Among FDA inspectors, senior or specialized inspectors, such as those overseeing complex manufacturing facilities or with advanced certifications, tend to earn higher salaries. Experience, certifications, and geographic location also influence pay levels for FDA inspectors. Generally, inspectors with specialized skills or leadership roles earn the most in this field.

Is it hard to get a job at FDA?

Becoming an FDA inspector can be competitive due to strict qualification requirements, including relevant experience, education, and passing civil service exams. Candidates often need a background in science, public health, or regulatory compliance, along with strong attention to detail and communication skills. The hiring process can be lengthy and involves multiple steps such as interviews and background checks.

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 manufacturing. They must pass a written exam and a background check, and often complete on-the-job training or specialized FDA training programs. Certification or licensing is not required but can enhance prospects.

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? For Fda Inspector jobs in Atlanta, GA, the most frequently searched job titles are:
What job categories do people searching Fda Inspector jobs in Atlanta, GA look for? The top searched job categories for Fda Inspector jobs in Atlanta, GA are:
What cities near Atlanta, GA are hiring for Fda Inspector jobs? Cities near Atlanta, GA with the most Fda Inspector job openings:
Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in Atlanta, GA as of July 2026, with employment types broken down into 87% Full Time, 10% Part Time, 2% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $54,508 per year, or $26.2 per hour.

Quality Assurance Inspector - Osmotica Pharmaceuticals

Osmotica

Marietta, GA • On-site

Full-time

Re-posted 10 days ago

Job description

Position Overview

The Quality Inspector is primarily responsible for supporting activities on the production floor. This includes room release, line clearance, in-process batch record review or post-executed review to ensure proper good documentation practices are followed. Provide quality oversight to all production areas to ensure product quality and compliance to cGMPs. This person works closely with operations personnel ensuring cGMP concerns are identified and resolved appropriately. Must be available/flexible to work second or third shift and weekends.

Duties and Responsibilities

  • Required to be on-the-floor and present to provide quality oversight for all critical manufacturing and packaging processes.
  • Perform QA release and line clearance inspections, AQL checks on product.
  • Perform Label Control functions (issuance and reconciliation).
  • Perform testing of incoming printed labeling materials
  • Conduct review of batch records.
  • Perform sampling of the Purified Water System
  • Identify deviations and ensure investigations are initiated by the appropriate personnel.
  • Clearly communicate complex issues to Management personnel.
  • Support creation / revision of SOPs to reflect current practices.
  • Assist with FDA and other regulatory inspections.
  • Perform all activities in compliance with Osmotica Quality System, site environmental, health and safety rules; and applicable FDA and international regulations.
  • Maintain knowledge of current regulatory requirements pertaining to drug product manufacture.
  • Perform additional duties and responsibilities as assigned.

Core Competencies

  • Position requires the ability to work independently and effectively in all areas of communication, collaboration, and decision-making.
  • Great attention to detail with ability to work on multiple projects.
  • Ability to organize and adapt to organization priority changes and work effectively with minimal supervision / independently with a sense of urgency.
  • Collaborate with Production, Warehouse and other QA team members as partners.
  • Computer experience required; Proficiency in Microsoft Office (Word, Excel).

Experience and Qualifications

  • High School Diploma or equivalent or technical school certificate.
  • Two years of experience in, or support of, pharmaceutical or biotech GMP manufacturing.
  • Proficient knowledge of a GMP production facility, manufacturing processes, and/or inspection processes.
  • Demonstrated understanding and application of cGMP, current industries practices and relevant guidance.
  • Excellent written and verbal communication skills.
  • Ability to multi-task effectively.
  • Quality Assurance experience a plus.

Apply