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Fda Inspector Jobs in Tennessee (NOW HIRING)

Lincare

Delivery Driver - Medical Equipment

Johnson City, TN · On-site

$17.25 - $21/hr

Inspect and maintain company-provided delivery vehicle, ensuring safety during the loading and ... Maintain cleanliness and organization of delivery vehicle and warehouse, adhering to all FDA ...

Lincare

Delivery Driver - Medical Equipment

Sevierville, TN · On-site

$15.25 - $18.75/hr

Inspect and maintain company-provided delivery vehicle, ensuring safety during the loading and ... Maintain cleanliness and organization of delivery vehicle and warehouse, adhering to all FDA ...

Lincare

Delivery Driver - Medical Equipment

Greeneville, TN · On-site

$15.50 - $19/hr

Inspect and maintain company-provided delivery vehicle, ensuring safety during the loading and ... Maintain cleanliness and organization of delivery vehicle and warehouse, adhering to all FDA ...

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All JobsFda Inspector JobsFda Inspector Jobs in Tennessee

Fda Inspector information

See Tennessee salary details

$22.2K

$49.9K

$89.9K

How much do fda inspector jobs pay per year?

As of Aug 21, 2026, the average yearly pay for fda inspector in Tennessee is $49,864.00, according to ZipRecruiter salary data. Most workers in this role earn between $34,900.00 and $57,600.00 per year, depending on experience, location, and employer.

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 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.

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.

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 a written exam and a background check, and often undergo specialized training at the FDA's training center. Certification or licensing is not required but can enhance prospects in the field.

What are the most commonly searched types of Fda Inspector jobs in Tennessee?

The most popular types of Fda Inspector jobs in Tennessee are:

What are popular job titles related to Fda Inspector jobs in Tennessee?

For Fda Inspector jobs in Tennessee, the most frequently searched job titles are:

What job categories do people searching Fda Inspector jobs in Tennessee look for?

The top searched job categories for Fda Inspector jobs in Tennessee are:

Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in Tennessee as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, 2% Contract, and 1% Nights. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $49,864 per year, or $24 per hour.

Product Quality Assurance Supervisor

August Bioservices

Nashville, TN • On-site

Full-time

Re-posted 5 days ago

Job description

Headquartered in Nashville, TN - one of the fastest-growing and most exciting cities in the United States - August Bioservices is a privately-owned, high-growth, and high-impact Contract Development Manufacturing Organization (CDMO).  As a US-based outsourcing partner that provides a wide array of expert drug discovery, drug formulation, and drug manufacturing services to pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our work is instrumental in helping to develop molecules today that can become the life-changing therapies of tomorrow. To support our growth plans, August is investing significant capital in a two-phase expansion project - including building a new state-of-the-art facility adjacent to our current facility. For those seeking dynamic opportunities, rewarding career paths and a chance to make a difference in global health, come grow with August!

The Product Quality Assurance Supervisor is responsible for the daily leadership and execution of the Acceptable Quality Level (AQL) and Quality on the Floor (QAOTF) programs. This position provides direct supervision of QA Specialists supporting manufacturing operations, ensuring continuous quality oversight of production activities, visual inspection programs, and real-time GMP compliance. 
The Supervisor serves as the primary Quality representative supporting manufacturing operations across all production shifts while driving consistent execution of QAOTF activities. 
ESSENTIAL DUTIES & RESPONSIBILITIES

  • Directly supervise the AQL and Quality on the Floor teams. 

  • Provide coaching, mentoring, performance management, and employee development. 

  • Manage staffing, scheduling, workload balancing, and shift coverage to support manufacturing operations, including evenings and weekends. 

  • Conduct performance evaluations and establish development plans. 

  • Ensure effective QA presence during manufacturing operations. 

  • Provide real-time GMP oversight of production activities. 

  • Ensure manufacturing follows approved batch records, SOPs, and GMP requirements. 

  • Escalate quality concerns to QA Management as appropriate. 

  • Manage the Quality Assurance AQL and visual inspection program. 

  • Ensure inspection activities are performed in accordance with approved procedures. 

  • Maintain AQL visual inspection qualification programs. 

  • Partner with Manufacturing to establish inspection standards and qualification requirements. 

  • Monitor inspection trends and recommend process improvements. 

  • Partner with Manufacturing leadership to coordinate QAOTF support. 

  • Ensure appropriate QA coverage for production schedules. 

  • Support and review investigations, deviations, CAPAs, and change controls impacting manufacturing operations. 

  • Support batch record review and batch disposition/release activities. 

  • Participate in production meetings and provide Quality input. 

  • Ensure compliance with FDA, EMA, ICH, and company procedures. 

  • Identify compliance risks and implement corrective actions. 

  • Assist with internal audits, client audits, and regulatory inspections. 

  • Track and report department metrics including inspection effectiveness, QA observations, and compliance trends. 

  • Recommend improvements to QAOTF processes and inspection programs. 

  • Communicate quality issues promptly to the Product QA Manager. 

  • Build collaborative relationships across Manufacturing, QC, Validation, Engineering, and Supply Chain. 

  • Promote a quality-focused culture throughout manufacturing operations. 

KNOWLEDGE, SKILLS, & ABILITIES

  • GMP compliance knowledge including knowledge of 21CFR210, 211, 820 and the PICS Guide to Good Manufacturing Practices Part 1 and 2 or the EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use, including Annex 1 and FDA Guidance on Aseptic Processing and Part 11 compliance knowledge preferred. 

  • Root Cause Analysis Tools, Risk Management, Technical Writing, Microsoft Office applications, eQMS and LIMS systems 

  • Experience with visual inspection, AQL programs, deviations, CAPAs, and manufacturing support activities. 

  • Strong communication, leadership, and organizational skills. 

QUALIFICATIONS
Master's Degree and 2+ years' experience in Quality Assurance or a DEA related field within a biotechnology, biologics, or pharmaceutical manufacturing facility OR Bachelor's Degree and 3+ years' experience in Quality Assurance or a DEA related field within a biotechnology, biologics, or pharmaceutical manufacturing facility. 
At August Bioservices, Our Credo is our culture. Everything we do, we do with great care. We believe in the promise of discovery and the power of science to transform lives. We assert that excellence is not a static destination, but a standard, and an every-day measuring stick of our advancement. We aspire to unlock the potential in every person, every process and every molecule - from start to finish. We are committed to doing the right thing the first time and every time, meeting or exceeding all regulatory requirements. We strive to be exceptional, preferred and indispensable partners for our customers; responsible and engaged citizens within our communities; and active, mindful stewards of our environment.
 
We are August Bioservices. We are pointing the way forward. If this sounds like your kind of working environment, we want you on our team!

August Bioservices  is an equal opportunity employer and values diversity. All aspects of employment including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs. August Bioservices does not discriminate on the basis of any status protected under federal, state, or local law.
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.
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