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Fda Jobs in Ohio (NOW HIRING)

R10095760 FDA Compliance Specialist (Open) Location: Independence, OH - Rockside Woods Blvd - Management - North BSCHorsham, PA (Regional Office) - Management, Waterford, CT (Regional Office ...

R10095760 FDA Compliance Specialist (Open) Location: Independence, OH - Rockside Woods Blvd - Management - North BSCHorsham, PA (Regional Office) - Management, Waterford, CT (Regional Office ...

R10095760 FDA Compliance Specialist (Open) Location: Independence, OH - Rockside Woods Blvd - Management - North BSCHorsham, PA (Regional Office) - Management, Waterford, CT (Regional Office ...

R10095760 FDA Compliance Specialist (Open) Location: Independence, OH - Rockside Woods Blvd - Management - North BSCHorsham, PA (Regional Office) - Management, Waterford, CT (Regional Office ...

$71K/yr

R10095760 FDA Compliance Specialist (Open) Location: Independence, OH - Rockside Woods Blvd - Management - North BSCHorsham, PA (Regional Office) - Management, Waterford, CT (Regional Office ...

... FDA, and international regulatory submissions, with technical review of data and reports • Assists in communication with regulatory agencies via pre-submissions and responses to premarket ...

In this high-impact role, you will ensure compliance with FDA, ISO 9001, ISO 13485, CE, and other applicable standards, while partnering with Manufacturing, Engineering, Supply Chain, and Regulatory ...

Clinical Research Coordinator

Cincinnati, OH · On-site

$23.25 - $31/hr

Complies with all IRB/FDA requirements in study submission. Assures compliance with IRB/FDA standards and deadlines in notification of subject randomization and enrollment. Assures compliance with ...

Clinical Research Coordinator

Cincinnati, OH · On-site

$23.25 - $31/hr

Complies with all IRB/FDA requirements in study submission. Assures compliance with IRB/FDA standards and deadlines in notification of subject randomization and enrollment. Assures compliance with ...

Clinical Research Coordinator

Cincinnati, OH · On-site

$23.25 - $31/hr

Complies with all IRB/FDA requirements in study submission. Assures compliance with IRB/FDA standards and deadlines in notification of subject randomization and enrollment. Assures compliance with ...

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 ...

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Fda information

See Ohio salary details

$12

$35

$70

How much do fda jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for fda in Ohio is $35.97, according to ZipRecruiter salary data. Most workers in this role earn between $22.41 and $44.83 per hour, depending on experience, location, and employer.

What does an FDA professional do?

An FDA professional works for the U.S. Food and Drug Administration, a federal agency responsible for protecting public health by ensuring the safety and efficacy of drugs, medical devices, food, cosmetics, and other products. Their roles can include reviewing and approving new drugs and medical devices, conducting inspections, enforcing regulations, and providing guidance to industries. FDA professionals may also work in research, policy development, and public outreach to ensure that products meet regulatory standards and are safe for consumer use.

What are the key skills and qualifications needed to thrive as an FDA Regulatory Affairs Specialist, and why are they important?

To thrive as an FDA Regulatory Affairs Specialist, you need a strong background in life sciences, regulatory guidelines, and compliance, usually supported by a relevant degree such as pharmacy, biology, or chemistry. Familiarity with regulatory submission systems, FDA regulations (such as 21 CFR), and certifications like RAC (Regulatory Affairs Certification) are highly beneficial. Attention to detail, strong analytical thinking, and effective communication skills help professionals navigate complex regulations and collaborate with cross-functional teams. These competencies ensure that products meet legal requirements and safety standards, facilitating successful approvals and market access.

What are some typical challenges faced by professionals working at the FDA, and how can they be managed?

Professionals at the FDA often navigate complex regulatory requirements, tight deadlines, and the need to balance public health priorities with industry innovation. Collaborating across multidisciplinary teams and staying updated on evolving scientific data are essential parts of the role. Adapting to frequent changes in policy and handling high volumes of submissions can be demanding, but leveraging strong communication skills and seeking mentorship within the agency can help manage these challenges effectively.

What is the difference between Fda vs Food Scientist?

AspectFdaFood Scientist
Required CredentialsTypically a degree in health, science, or related field; certifications varyBachelor's or master's in food science, microbiology, or related
Work EnvironmentRegulatory agencies, laboratories, inspection sitesFood manufacturing facilities, laboratories, research settings
Employer & Industry UsageU.S. Food and Drug Administration, government agenciesFood companies, research institutions, government agencies
Common Search & Comparison IntentUnderstanding regulatory roles, compliance, and enforcementFood safety, product development, research

While both Fda professionals and Food Scientists work within the food industry, Fda roles focus on regulation, compliance, and enforcement of food safety laws, often within government agencies. Food Scientists primarily engage in research, product development, and ensuring food quality in manufacturing settings. The two careers overlap in food safety knowledge but differ in their primary responsibilities and work environments.

What qualifications do you need to work for the Food and Drug Administration?

To work for the Food and Drug Administration (FDA), candidates typically need a bachelor's degree in a relevant field such as science, engineering, or public health. For certain positions, advanced degrees or specialized certifications may be required, along with relevant work experience and knowledge of regulatory processes and compliance standards.

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

The most popular types of Fda jobs in Ohio are:

What cities in Ohio are hiring for Fda jobs?

Cities in Ohio with the most Fda job openings:

Infographic showing various Fda job openings in Ohio as of August 2026, with employment types broken down into 76% Full Time, 6% Part Time, and 18% Contract. Highlights an 100% In-person job distribution, with an average salary of $74,815 per year, or $36 per hour.

FDA Compliance Specialist

Independence, OH • On-site


Airgas
Chemical Manufacturing • 10K+ employees

7.8

Company rating: 7.8 out of 10

Based on 221 frontline employees who took The Breakroom Quiz

90th of 366 rated logistics

People enjoy working here

Good employer

Recommended by parents


$10K/mo

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago


Job description

R10095760 FDA Compliance Specialist (Open)
Location:
Independence, OH - Rockside Woods Blvd - Management - North BSCHorsham, PA (Regional Office) - Management, Waterford, CT (Regional Office) - Management - Northeast Region
How will you CONTRIBUTE and GROW?
We are committed to building a diverse and inclusive workplace that embraces the unique perspectives of our employees, our customers, patients, community stakeholders, and cultures across the world. We believe that a variety of backgrounds makes our team stronger and more innovative.
At Airgas, we RESPECT, HONOR and VALUE diversity.
Airgas is Hiring for a FDA Compliance Specialist in Independence, OH!
We are looking for you!
  • $ 71,000- $106,00
  • Monthly Auto Allowance
  • Hybrid Schedule
  • Comprehensive Family Benefits: Airgas offers a full benefits package designed to support your whole life, including Medical, Dental, Vision, Life, AD&D, and Disability Insurance.
  • Support for Parents:We offer up to 14-week paid child birth benefits to support growing families.
  • Future Security:401(k) Retirement Plan with company match, Tuition Assistance, Paid Holidays, Vacation, and Sick time.
  • Early Access: Your benefits start after just 30 days of employment

Recruiter: Sophia Harris | sophia.harris-sc@airgas.com | (656) 263-5716 (Call/Text)
Focuses on ensuring the Division's compliance with Food, Drug and Device regulations which is supported by a thorough understanding and working knowledge of the current Airgas Medical SOP's and Food Gas Manual, and collaborates to apply these SOPs to the food, drug and device manufacturing process. Additionally, working knowledge and understanding of current good manufacturing practice in manufacturing, processing, packing and/or holding drugs and devices, current good manufacturing practice for finished pharmaceuticals, and a firm understanding of the FDA's GRAS (generally recognized as safe) requirements for food products.
To perform this job successfully, an individual will be supported in performing each essential duty satisfactorily. The qualifications we are looking for below are representative of the knowledge, skill, and/or ability highly valued. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
  • Partner to guide and support the Quality Department's general FDA compliance activities including compliance auditing and regulatory assistance.
  • Provide specialized guidance to ensure compliance with all applicable Federal and State requirements regulating the manufacturing and distribution of drug, device and food products.
  • Develops and maintains strong partnerships with operations, distribution, and sales leadership in assigned region to develop, champion, implement and sustain Quality and FDA Compliance strategies, policies, standards, guidelines, processes and optimized practices. Work with global peers to develop optimized practices as it relates to the overall quality & compliance system.
  • Actively participates in the development of training materials and trains members of the local Quality Control Unit (QCU) in areas of Current Good Manufacturing Practices (cGMPs) with the shared understanding of the "WHY" we do what we do.
  • Performs physical audits annually, and monthly paper audits of drug, device and food manufacturing facilities with the emphasis of analyzing the process to ensure that it conforms to Airgas Medical Drug gas SOPs.
  • Represent Airgas during on-site inspections by the FDA, other government agencies, and customers.
  • Maintain specialized guidance regarding current and developing food, drug, and standards and regulations and how they impact Airgas' business and quality system.
  • Assist in assuring and sustaining compliance with all regulatory requirements associated with medical products and processes.
  • Review and approve validation protocols and final reports.
  • Assist plants with regulatory and customer audits of manufacturing facilities.
  • Conducts follow-up reviews to ensure the completion of required corrective actions and continued plant compliance to SOPs.
  • Drafts corrective action responses associated with state, federal and customer audits observations, and reviews these with FDA Divisional Director before release.
  • Creates deviation requests and submits these to Division Director of FDA Compliance for review.
  • Coordinates the investigation of serious medical complaints.
  • Ensures that any procedural revisions are communicated to the manufacturing facilities and training is conducted.
  • Assist in providing compliance audit and Annual Product Review feedback to business entity leadership.
  • Assess progress toward Quality standards and champion suggestions for continuous improvement.
  • Additional duties and projects as may be assigned.

Are you a MATCH?
Required Qualifications:
  • High school diploma or equivalent
  • A minimum of 3 years of experience actively auditing locations, partnering with business leaders, championing change and representing their company during audits.
  • Demonstrated knowledge and experience working with Industrial and medical gases experience especially with oxygen, nitrogen and CO2 processes are required.
  • Knowledge of local, state and federal laws pertaining to production of drugs and medical devices is required.
  • Prior experience working with FDA compliance rules and regulations is required.
  • Demonstrated experience resolving compliance and regulatory issues in collaboration with business leadership, agencies, and public interest groups is required
  • Must be proficient in Word, Excel, PowerPoint and Google Suites.
  • Planned and unplanned overnight travel up to 50 - 60%.

Preferred Qualifications:
  • College degree highly preferred.
  • Previous work experience in the GXP/FDA controlled environments a plus.
  • Experience working in a multi-state distribution/retail organization is desired.

Benefits
We care about and support our Airgas Families. This is evident not only through our competitive compensation but also through a comprehensive benefits package that includes medical, dental, and vision plans, short-term and long-term disability, life and accidental death and dismemberment (AD&D) insurance, Employee Assistance Program (EAP), pre-tax commuter transportation benefit, parental leave, vacation, sick time, floating holidays, jury duty and funeral/bereavement leave, and paid holidays for all eligible full-time employees.
Additionally, we offer our eligible employees a 401k plan with company matching funds, tuition reimbursement, discounted college tuition for eligible employees' dependents, and an Airgas Scholarship Program for dependent children.
Associates who are members of collective bargaining units should review their bargaining agreement to determine whether they are eligible for some or all of the benefits described here and to see any special terms or conditions for eligibility.
Your DIFFERENCES enhance our PERFORMANCE
At Airgas, we are committed to building a workplace that embraces the diversity of our employees, our customers, patients, community stakeholders and cultures across the world.
We welcome and consider applications from all qualified applicants, regardless of their race, gender, sexual orientation, religion, disability or any other protected characteristic. We strongly believe a diverse organization opens up opportunities for people to express their talent, both individually and collectively and it helps foster our ability to innovate by living our fundamentals, acting for our success and creating an engaging environment in a changing world.
About Airgas
Airgas, an Air Liquide company, is a leading U.S. supplier of industrial, medical and specialty gases, as well as hardgoods and related products; one of the largest U.S. suppliers of safety products; and a leading U.S. supplier of ammonia products and process chemicals. Through the passion and diversity of its 18,000 associates, Airgas fosters a culture of safety, customer success, sustainability and innovation. Airgas associates are empowered to share ideas, take initiative and make decisions.
Airgas is a subsidiary of Air Liquide, a world leader in gases, technologies and services for industry and healthcare. Present in 60 countries with approximately 66,500 employees, Air Liquide serves more than 4 million customers and patients.
Join us for a stimulating experience: At Airgas, you matter and so does the work you do. As a member of our team, you play an important role in the success of your team, making sure our products are created sustainably and delivered safely and efficiently. In turn, you'll find a welcoming workplace where you're valued for who you are and where you can fill your potential while growing a fulfilling career - whatever path you choose.
Equal Employment Opportunity Information
We are an equal opportunity employer. We welcome all qualified applicants regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected characteristic.
Airgas, an Air Liquide Company is a Government contractor subject to the Vietnam Era Veterans' Readjustment Assistance Act of 1974 and Section 503 of the Rehabilitation Act of 1973.
Airgas does not discriminate against qualified applicants with disabilities, and is committed to providing reasonable accommodations to the known disabilities of such individuals so as to ensure equal access to benefits and privileges of employment. If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please contact us by email at us-accommodationrequest@airgas.com.
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About Airgas

Sourced by ZipRecruiter

Airgas, an Air Liquide company, is a leading U.S. supplier of industrial, medical and specialty gases, as well as hardgoods and related products; one of the largest U.S. suppliers of safety products. Through the passion and diversity of its 18,000 associates, Airgas fosters a culture of safety, customer success, sustainability and innovation. Airgas associates are empowered to share ideas, take initiative and make decisions. Join us for a stimulating experience: you'll find a world of learning and development opportunities where inventiveness is at the heart of what we do, in an open, collaborative and respectful environment.

Industry

Chemical manufacturing

Company size

10,000+ Employees

Headquarters location

Radnor, PA, US

Year founded

1982

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Hours and flexibility

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