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Full Time Fda Inspector Jobs in Ohio (NOW HIRING)

Katmai

Quality Assurance Manager

Brilliant, OH · On-site

$60K/yr

Conduct and participate directly in quality inspections, internal and external audits, and FDA ... WORK SCHEDULE Full-time, Monday-Friday day shift. No weekends. May be required to work additional ...

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Full Time Fda Inspector information

Is it hard to get hired by the FDA?

Getting hired as a full-time 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 related fields, along with strong attention to detail and knowledge of regulatory standards. The hiring process may involve multiple steps, including interviews and background checks.

What is the difference between Full Time Fda Inspector vs Part Time Fda Inspector?

AspectFull Time Fda InspectorPart Time Fda Inspector
CredentialsTypically requires a bachelor's degree in life sciences or related field, plus FDA inspector certificationSame as full-time, but may have more flexible certification requirements
Work EnvironmentFull-time, on-site inspections at manufacturing facilities, laboratories, and warehousesPart-time, often involves scheduled inspections or follow-ups
Employer & Industry UsageFDA, government agencies, regulated industriesFDA, contractors, or consulting firms

Full Time Fda Inspectors work primarily on-site, conducting regular inspections and ensuring compliance with FDA regulations. Part Time Fda Inspectors perform inspections on a flexible schedule, often supplementing full-time staff. Both roles require similar credentials but differ mainly in hours and scope of work.

What is the highest paying job at the FDA?

The highest paying job at the FDA is typically a senior leadership role such as the Director of the Center for Drug Evaluation and Research or the Director of the Center for Biologics Evaluation and Research, which can have salaries exceeding $180,000 annually. These positions require extensive experience, advanced degrees, and often involve overseeing regulatory policies and scientific review processes.

What type of inspectors make the most money?

In the inspection field, federal inspectors such as FDA inspectors or those working in highly regulated industries tend to earn higher salaries due to specialized knowledge and certification requirements. Senior inspectors with extensive experience, advanced certifications, or supervisory roles also typically earn more than entry-level inspectors. Salary levels can vary based on location, industry, and level of responsibility.

How do I become an FDA inspector?

To become a full-time FDA inspector, candidates typically need a bachelor's degree in a relevant field such as biology, chemistry, or food science, along with experience in regulatory compliance or quality assurance. Applicants must pass a competitive federal hiring process, which includes written exams and background checks, and may require specialized training provided by the FDA or other agencies.

What are the key skills and qualifications needed to thrive as a Full Time FDA Inspector, and why are they important?

To thrive as a Full Time FDA Inspector, you typically need a background in life sciences or a related field, strong analytical abilities, and knowledge of regulatory standards, often supported by a relevant bachelor's degree. Familiarity with inspection software, laboratory equipment, and FDA regulations, such as 21 CFR, is essential. Exceptional attention to detail, critical thinking, and effective communication skills help inspectors conduct thorough evaluations and collaborate with regulated entities. These skills ensure compliance with federal regulations, safeguarding public health and ensuring industry accountability.

What does a Full Time FDA Inspector do?

A Full Time FDA Inspector is responsible for ensuring that products regulated by the Food and Drug Administration (FDA)—such as food, drugs, medical devices, and cosmetics—comply with all applicable laws and regulations. They conduct inspections of manufacturing facilities, review processes for safety and quality, collect samples for laboratory analysis, and document their findings. Their work helps protect public health by identifying and addressing potential risks before products reach consumers.

What are some common challenges faced by Full Time FDA Inspectors during facility inspections?

Full Time FDA Inspectors often encounter challenges such as navigating complex manufacturing environments, ensuring compliance with evolving regulations, and effectively communicating findings to facility staff. Inspectors must balance thoroughness with efficiency, sometimes facing resistance or misunderstanding from inspected parties. Additionally, staying current on new product types and technologies can require ongoing training and adaptability, making collaboration with colleagues and subject matter experts essential.
What are the most commonly searched types of Fda Inspector jobs in Ohio? The most popular types of Fda Inspector jobs in Ohio are:
What cities in Ohio are hiring for Full Time Fda Inspector jobs? Cities in Ohio with the most Full Time Fda Inspector job openings:
Full Time Fda Inspector jobs near you
Infographic showing various Full Time Fda Inspector job openings in Ohio as of July 2026, with employment types broken down into 100% Full Time. Highlights an 98% In-person, and 2% Remote job distribution.
Senior Quality Control & Compliance Engineer

Senior Quality Control & Compliance Engineer

Rust Belt Recruiting

Newbury, OH

$85K - $100K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

Job description

Title: Senior Quality Control & Compliance Engineer

Shift: Condensed Schedule | 9 hours per day Monday through Thursday, 4 hours on Friday

Salary: $85,000 - $100,000 per year, plus performance-based bonus; exact compensation is dependent on experience

Senior Quality Control & Compliance Engineer Role:

Our client is seeking a detail-oriented professional to oversee day-to-day quality control operations and execute comprehensive compliance programs. This role exists to resolve quality issues, maintain Quality Management Systems, and satisfy ISO and FDA regulatory requirements to ensure product integrity across high-reliability electronics and medical devices.

Senior Quality Control & Compliance Engineer Responsibilities:

  • Collaborate with production, engineering, and supply chain teams to investigate and resolve quality issues

  • Handle the customer complaint process end-to-end through root-cause analysis, corrective actions, and documentation

  • Provide technical support to inspectors for incoming material and finished product quality checks on electronic devices, cable assemblies, and medical products

  • Create, review, and maintain quality documentation including procedures, inspection plans, quality records, and device history files

  • Monitor and report on key quality metrics like defect rates and complaint trends to contribute to process improvements

  • Execute and maintain elements of the Quality Management System (QMS) in accordance with ISO 9001 and ISO 13485 standards

  • Support FDA compliance activities for medical device production

  • Lead internal audits, customer audits, and third-party certification audits while assisting with preparation for FDA inspections

  • Maintain regulatory filings, technical documentation, and quality records to ensure they remain current and audit-ready

Senior Quality Control & Compliance Engineer Reporting Relationships:

The Senior Quality Control & Compliance Engineer reports directly to the Engineering Manager. This position functions as an individual contributor and technical mentor without direct supervisory reports.

About You:

  • Possess a Bachelor's degree in Engineering, Quality Assurance, Regulatory Affairs, or a related technical field (or equivalent experience)

  • Hold a minimum of 5 years of experience in quality and compliance within electronics manufacturing, preferably with medical devices and cable/electronic assemblies

  • Demonstrate solid working knowledge of ISO 9001, ISO 13485, and FDA Quality System Regulation (QSR) requirements

  • Exhibit proven experience supporting quality inspections, managing customer complaints, and creating quality documentation

  • Demonstrate strong organizational, communication, and problem-solving skills with high attention to detail

  • Maintain the ability to work collaboratively within a team environment while maintaining individual accountability

  • Hold preferred credentials such as ASQ certifications (CQE, CQA) or regulatory affairs certifications (RAC)

  • Demonstrate preferred familiarity with risk management (ISO 14971), validation processes, and statistical quality tools like SPC and Gage R&R

  • Possess the ability to commute daily in-person to Newbury, OH 44065

Next Steps:

If you are a self-motivated problem-solver and detail-oriented professional, we would like to hear from you. Please reach out to our recruiting agency today to discuss this opportunity with our client.

Additional Information:

  • Equal Opportunity Employer: Our client provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, or genetics

  • Working Conditions: This is a full-time, in-person role located at the facility in Newbury, OH 44065

  • Benefits Package: Position offers a comprehensive benefits package including health, dental, vision, HSA, life insurance, 401(k) with match, paid time off, and company holidays

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