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Full Time Fda Inspector Jobs in Ohio (NOW HIRING)

Latitude 36 Foods

Sanitarian Lead

West Chester, OH · On-site

$17.75 - $23/hr

West Chester, OH Position Type: Full Time Shift: 3rd shift Rate: Hourly Classification: Non-Exempt ... USDA Inspection experience. * Bilingual Spanish/English a plus. * USDA Sanitation experience, at ...

Ecowize USA

Sanitation Technician

Northwood, OH · On-site

$15.75 - $19/hr

... FDA, and customer standards. This is a physical role that requires focus, teamwork, and ... Inspect equipment and areas to confirm readiness for pre-op inspections. * Follow all company and ...

Ecowize USA

Sanitation Technician

Harrison, OH · On-site

$15.75 - $19/hr

... FDA, and customer standards. This is a physical role that requires focus, teamwork, and ... Inspect equipment and areas to confirm readiness for pre-op inspections. * Follow all company and ...

Latitude 36 Foods

Sanitarian Lead

West Chester, OH · On-site

$17.75 - $23/hr

West Chester, OH Position Type: Full Time Shift: 3rd shift Rate: Hourly Classification: Non-Exempt ... USDA Inspection experience. * Bilingual Spanish/English a plus. * USDA Sanitation experience, at ...

DSV A/S

Quality Assurance Specialist

Cleveland, OH · On-site

Quality Assurance Specialist - 121786 Time Type: Full Time As a Quality Assurance Specialist at DSV ... Conduct internal audits and inspections to assess compliance with quality standards, procedures ...

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Full Time Fda Inspector information

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 are the key skills and qualifications needed to thrive as a full time FDA inspector?

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 August 2026, with employment types broken down into 100% Full Time. Highlights an 98% In-person, and 2% Remote job distribution.

Strategist, Regulatory Affairs

ClinChoice

Cincinnati, OH • On-site

Full-time

Posted 3 days ago

New

Job description

ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative "one-team" culture. We are looking for a dynamic person to join our in-house team as a Associate, Regulatory Affairs (ONSITE) on a permanent basis at Cincinnati, OH.
Join our team: you can be part of making a difference in peoples' lives and experience a fulfilling and rewarding career!
Job Title: Strategist, Regulatory Affairs
Employment Type: Full Time
Location: Hybrid (Cincinnati, Ohio) - Location Address: 4545 Creek Rd Blue Ash, OH 45242
  • Responsible for managing, planning, preparation, and delivery of documents both electronic- and paper-based in support of assigned. global regulatory product registrations, renewals, tenders/customs, etc.
  • Coordinate the preparation and submission of medical device applications by providing regulatory information and documents and following up closely on queries from inspection through approval.
  • Prepare and/or review letters of authorization, cover letters for registration certificates, declarations, power of attorney, and other regulatory documentation to ensure accuracy, appropriateness, and consistency of documents intended for various global regulatory submissions.
  • Submit and manage applications for the US FDA Certificates to Foreign Government (CFGs).
  • Maintain various tracking tools to ensure up-to-date information and traceability of all regulatory data/documentation.
  • Perform and/or coordinate legalization, notarization, and apostille of regulatory documents
  • Ensure compliance with current good documentation practices, including but not limited to proofreading, formatting, indexing and recordkeeping.
  • Assist all regions in answering inquiries and providing required documents and information utilizing various search tools and systems.
  • Perform document filing and retrieval functions as directed and per company's policies and procedures.
  • Effectively communicate with internal and external teams and/or clients as to the status of deliverables, to ensure timely and satisfactory completion of tasks and expectations.
  • Communicate with the project teams on a regular basis regarding regulatory updates.
  • Provide support to internal and external teams to address various technical inquiries and provide requested data/information
  • Participate in group meetings and provide tactical approaches to addressing issues of basic complexity
  • Perform other tasks as assigned.

Experience/Skills
  • Bachelor's degree (Life Sciences or a regulatory related field preferred)
  • Minimum of 1 year of hands-on experience in medical device regulatory affairs, or at least 3 years of combined regulatory affairs and related experience.
  • Basic knowledge of US FDA QSR, ISO 13485, EU MDD/MDR.
  • Knowledge of global medical devices registration process is a plus
  • Proficient in Microsoft Office (e.g., Word, Excel, PowerPoint)
  • Have a good understanding of current Good Documentation Practices in a regulatory environment.
  • Self-starter with the ability to work in a team environment and on projects of diverse scope where analysis of a situation or data requires evaluation of various factors with minimal supervision.
  • Excellent organizational skills with strong attention to detail, effective planning, and the ability to multitask efficiently
  • Must possess excellent written and verbal communication skills.

The Application Process
Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
Who will you be working for?
About ClinChoice
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Our Company Ethos
Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.
ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
#LI-PB1 #Hybrid

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