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Fda Inspector Jobs in Cleveland, OH (NOW HIRING)

Quality Inspector

Cleveland, OH ยท On-site

$28 - $32/hr

Our FDA 510(k)-cleared Dreem EEG headband and AI algorithms enable quantitative biomarker discovery ... We are looking for a detail-oriented, quality-focused Quality Inspector to join our Cleveland team.

Our FDA 510(k)-cleared Dreem EEG headband and AI algorithms enable quantitative biomarker discovery ... We are looking for a detail-oriented, quality-focused Quality Inspector to join our Cleveland team.

Acting as the management representative for FDA and ISO 13485 inspections * Manage and administer the CAPA process for both Invacare and Invamex, ensuring timely initiation, tracking, investigation ...

... FDA 21 CFR Part 820/211, EU MDR, and other applicable regulatory standards. This role coordinates document control transactions, site record retention, calibration and inspection activities. In ...

... clean, FDA-regulated environment while collaborating with skilled operators and using computer ... Inspect pharmaceutical products visually to ensure they meet quality standards and are free from ...

Strong attention to detail for inspection, labeling, and packaging tasks. Additional Skills & Qualifications * Experience working in an FDA-regulated environment is a plus. * Familiarity with Good ...

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Fda Inspector information

See Cleveland, OH salary details

$23.8K

$53.3K

$96K

How much do fda inspector jobs pay per year?

As of Jul 27, 2026, the average yearly pay for fda inspector in Cleveland, OH is $53,282.00, according to ZipRecruiter salary data. Most workers in this role earn between $37,300.00 and $61,600.00 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 the most commonly searched types of Fda Inspector jobs in Cleveland, OH? The most popular types of Fda Inspector jobs in Cleveland, OH are:
What are popular job titles related to Fda Inspector jobs in Cleveland, OH? For Fda Inspector jobs in Cleveland, OH, the most frequently searched job titles are:
What cities near Cleveland, OH are hiring for Fda Inspector jobs? Cities near Cleveland, OH with the most Fda Inspector job openings:
Infographic showing various Fda Inspector job openings in Cleveland, OH as of July 2026, with employment types broken down into 85% Full Time, 12% Part Time, 2% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $53,282 per year, or $25.6 per hour.
Quality Inspector

Quality Inspector

Beacon Biosignals

Cleveland, OH โ€ข On-site

$28 - $32/hr

Full-time

Posted 17 days ago


Job description

What you will be doing:
Beacon Biosignals is on a mission to revolutionize precision medicine for the brain. We are the leading at-home EEG platform supporting clinical development of novel therapeutics for neurological, psychiatric, and sleep disorders. Our FDA 510(k)-cleared Dreem EEG headband and AI algorithms enable quantitative biomarker discovery and implementation. Beacon's Clinico-EEG database contains EEG data from nearly 100,000 patients, and our cloud-native analytics platform powers large-scale RWD/RWE retrospective and predictive studies. Beacon Biosignals is changing the way that patients are treated for any disorder that affects brain physiology.
We are looking for a detail-oriented, quality-focused Quality Inspector to join our Cleveland team. This role is a critical checkpoint in the manufacturing process, maintaining accurate documentation in accordance with Good Documentation Practices, and flagging nonconformances early. You'll report to Quality Engineering, supporting audits, complaint investigations, and equipment upkeep, while helping drive continuous improvement across the quality system.
This is a hands-on, in-person role ideal for someone who takes pride in precision, stays disciplined about process and documentation, and genuinely cares about product quality and patient safety.
This role is a contract role required to work from the Cleveland office 5 days a week.
$28.00 - $32.00/hour
What success looks like:
  • Performing incoming and final inspection of components, subassemblies, and finished devices against drawings, specifications, and work instructions
  • Recording inspection results and maintaining accurate, complete records (including Device History Records) in accordance with Good Documentation Practices (GDP)
  • Identifying nonconforming material and escalating findings to Quality Engineering per established nonconformance procedures
  • Performing monthly quality inspections of the manufacturing areas to ensure compliance with SOPs and work instructions
  • Supporting Quality Engineering with document control, audits, and complaint investigations, as directed
  • Assisting with equipment upkeep, including flagging equipment due for calibration
  • Staying current on assigned work instructions, SOPs, and applicable quality system requirements relevant to the inspection role
  • Participating in continuous improvement and quality initiatives under the direction of Quality Engineering

What you will bring:
  • 1-2 years of experience performing quality inspection in a medical device or other regulated manufacturing environment
  • High school diploma or equivalent required; Associate's degree in a technical or scientific field preferred
  • Working knowledge of Good Documentation Practices (GDP) and familiarity with quality system requirements (e.g., 21 CFR 820, ISO 13485) as they apply to inspection and record-keeping
  • Strong attention to detail and accuracy, particularly in documentation and data recording
  • Comfortable working under established procedures and escalating issues
  • Good communication skills and ability to work well within a team, taking direction from Quality Engineering

At Beacon, we've found that cultural and scientific impact is driven most by those that lead by example. As such, we're always seeking new contributors whose work demonstrates an avid curiosity, a bias towards simplicity, an eye for composability, a self-service mindset, and - most of all - a deep empathy towards colleagues, stakeholders, users, and patients. We believe a diverse team builds more robust systems and achieves higher impact.