ZipRecruiter

Log In

1

Fda Inspector Jobs in Oklahoma (NOW HIRING)

IMMY

Regulatory Affairs Specialist - FDA

Norman, OK · Remote

Maintain regulatory records, submission files, FDA correspondence, and other data and files inspection-ready for audit by FDA or other regulatory authorities or authorized third parties * Comply with ...

Del Real Llc

Safety Lead

Moore, OK · On-site

$55 - $75/hr

This role assists with implementing safety programs, conducting inspections, responding to incidents, and providing training. The Safety Lead promotes compliance with OSHA, USDA, FDA, and SQF ...

DEL REAL LLC

Safety Lead

Moore, OK · On-site

$19/hr

This role assists with implementing safety programs, conducting inspections, responding to incidents, and providing training. The Safety Lead promotes compliance with OSHA, USDA, FDA, and SQF ...

Lincare

Delivery Driver - Medical Equipment

Oklahoma City, OK · On-site

$14.75 - $18.25/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

Lawton, OK · On-site

$13.50 - $16.75/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 ...

Refresco

Sanitation Technician

Fort Gibson, OK · On-site

$15.50 - $18.75/hr

... FDA, SQF, etc). * Prepare production equipment for cleaning and follow necessary lock out/tag out ... Verifies and validates sanitation effectiveness with visual inspection and chemical concentration ...

nexAir

Route Driver

Tulsa, OK · On-site

$16.50 - $21.50/hr

... trip inspections per DOT regulations. • Complete all FDA/DOT required documentation. • Track delivery and pick-up of cylinders at customer sites using handheld device and complete all the ...

next page

Showing results 1-20

All JobsFda Inspector JobsFda Inspector Jobs in Oklahoma

Fda Inspector information

See Oklahoma salary details

$22.6K

$50.7K

$91.4K

How much do fda inspector jobs pay per year?

As of Sep 5, 2026, the average yearly pay for fda inspector in Oklahoma is $50,727.00, according to ZipRecruiter salary data. Most workers in this role earn between $35,500.00 and $58,600.00 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 popular job titles related to Fda Inspector jobs in Oklahoma?

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

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

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

Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in Oklahoma as of August 2026, with employment types broken down into 90% Full Time, 5% Contract, and 5% Nights. Highlights an 100% In-person job distribution, with an average salary of $50,727 per year, or $24.4 per hour.

Regulatory Affairs Specialist - FDA

Immuno-Mycologics, Inc.

Norman, OK • On-site

Full-time

Posted 17 days ago

Job description

Job Type
Full-time
Description
*This is a remote-eligible position, requiring the candidate live within the U.S.
Job Purpose
The Regulatory Affairs Specialist - FDA is responsible for preparing and maintaining U.S. FDA regulatory submissions for IMMY's in vitro diagnostic products, and for securing and maintaining the clearances, registrations, listings, and licenses required to place and keep those products on the U.S. market.
Key duties and responsibilities
Bring New Products to the U.S. Market
  • Determine the appropriate U.S. regulatory pathway for IMMY's products, including classification, product code selection, and predicate identification
  • Prepare and submit 510(k), PMA, De Novo, and Emergency Use Authorization submissions (as applicable), along with the technical documentation supporting each marketing authorization
  • Manage Q-Submissions and other formal interactions with FDA review divisions, including tracking review timelines and responding to Agency requests
  • Advise product development teams on FDA expectations for analytical and clinical performance data, including verification and validation study design

Keep Products Registered and Available
  • Monitor the U.S. regulatory status of the marketed portfolio on an ongoing basis to confirm that each product remains lawfully marketable, and identify and remediate any lapse or other issues with existing registrations, listings, licenses, or authorization.
  • Maintain establishment registration, device listing, UDI/GUDID data, and other institutional and/or product registrations related to U.S. market access.
  • Support post-market activities for marketed products, including reportability assessments, Medical Device Reports, field actions, and reports of corrections and removals

Maintain U.S. Regulatory Compliance
  • Review labeling, package inserts, instructions for use, and other materials for compliance with applicable regulations
  • Verify that promotional, marketing, and sales-facing materials remain consistent with the cleared or authorized intended use
  • Maintain regulatory records, submission files, FDA correspondence, and other data and files inspection-ready for audit by FDA or other regulatory authorities or authorized third parties
  • Comply with, and assist IMMY in complying with, all applicable FDA medical device regulatory requirements, applicable ISO 13485 requirements, and all other applicable laws, regulations, and standards
  • Monitor and assess the operational impact of regulatory changes affecting IMMY's processes and products available in the U.S., ensuring timely planning and implementation of any changes necessary for compliance

Qualifications
Required:
  • Bachelor's degree in related discipline and 2+ years of experience performing Regulatory Affairs support activities in a U.S. FDA regulated environment
  • Broad knowledge of U.S. FDA medical device regulations and their application to IVDs
  • Broad knowledge of ISO 13485 standards requirements
  • Effective technical writing and oral communication skills
  • Extremely organized with high attention to detail
  • Effective at multi-tasking
  • Ability to work in a fast-paced, timeline-driven environment
  • Ability to work independently and as part of a team
  • Ability to organize information so that it is easily understood and reviewed, both internally and externally
  • Ability to identify ways to improve/simplify processes

Equal Opportunity Employment: IMMY is committed to the principle of equal employment opportunity for all employees and applicants for employment and prohibits discrimination and harassment of any kind without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, and local laws. IMMY will not tolerate discrimination or harassment based on any of these characteristics. This policy applies to all terms and conditions of employment, including, but not limited to, recruiting, hiring, promotion, termination, leaves of absence, compensation, and training.
Background Check Policy: All offers of employment at IMMY are contingent upon clear, acceptable results of a thorough background check. IMMY performs all background checks in compliance with EEOC and FCRA regulations and all other applicable federal, state, and local laws.

Apply