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Full Time Fda Tobacco Inspector Jobs in Riverside, CA

Jensen Meat Company Inc

QA Supervisor

Riverside, CA · On-site

Description FLSA Status: Full-Time / Non-Exempt Location: Jensen Meat Company - Otay Mesa, CA ... FDA regulated food manufacturing environment. (Dual inspection experience preferred) Strong ...

Prismatik

Regulatory Affairs Specialist, Sr.

Irvine, CA · On-site

$84K - $120K/yr

In this role, you'll lead FDA 510(k)/PMA filings, maintain international registrations, support ... Conducts audits and inspections of GMP and non-regulated documentation. * Tracks internal and ...

Latitude 36 Foods

Sanitation Supervisor

Corona, CA · On-site

$79K - $85K/yr

Corona, California Position Type: Full-time Classification: Exempt Shift: Flexible Salary Range ... inspections is preferred. * HACCP and SQF certifications are preferred. * FDA and/or USDA ...

Latitude 36 Foods

Sanitation Supervisor

Corona, CA · On-site

$79K - $85K/yr

Corona, California Position Type: Full-time Classification: Exempt Shift: Flexible Salary Range ... inspections is preferred. * HACCP and SQF certifications are preferred. * FDA and/or USDA ...

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All JobsFda Tobacco Inspector JobsFull Time Fda Tobacco Inspector JobsFull Time Fda Tobacco Inspector Jobs in Riverside, CA

Full Time Fda Tobacco Inspector information

See Riverside, CA salary details

$25.6K

$57.3K

$103.3K

How much do full time fda tobacco inspector jobs pay per year?

As of Aug 11, 2026, the average yearly pay for full time fda tobacco inspector in Riverside, CA is $57,316.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,200.00 and $66,200.00 per year, depending on experience, location, and employer.

What are common challenges faced by full time FDA tobacco inspectors?

Full Time FDA Tobacco Inspectors often encounter challenges such as staying current with evolving federal regulations and ensuring compliance across diverse retail environments. They may face resistance or lack of cooperation from retailers, requiring strong communication and conflict resolution skills. The role also demands meticulous attention to detail during inspections and accurate documentation, as well as frequent travel to assigned locations. Building relationships with local enforcement agencies and adapting to varying work schedules are also key aspects of the job.

What skills and qualifications are needed to be a full time FDA tobacco inspector?

To thrive as a Full Time FDA Tobacco Inspector, you need a background in regulatory compliance, investigative procedures, and typically a bachelor's degree in a related field such as public health or criminal justice. Familiarity with FDA inspection protocols, data collection tools, and reporting systems is crucial for accurate documentation and enforcement. Strong attention to detail, effective communication, and impartial judgment are vital soft skills for conducting thorough inspections and interacting with regulated entities. These competencies ensure the enforcement of tobacco regulations, protect public health, and maintain compliance with federal standards.

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

AspectFull Time Fda Tobacco InspectorPart Time Fda Tobacco Inspector
Work HoursTypically 40 hours/weekLess than 30 hours/week
CertificationsRequired FDA training and certificationsSame certifications, but may have less comprehensive training
Work EnvironmentFull-time inspection facilities, regulatory agenciesSimilar environments, often flexible or part-time schedules
Employer UsageConsistent employment with FDA or contractorsTemporary or supplemental roles within the industry

Full Time Fda Tobacco Inspectors work standard hours with full benefits, focusing on comprehensive inspections and regulatory compliance. Part Time Fda Tobacco Inspectors have flexible schedules, often with similar responsibilities but fewer hours. Both roles require FDA certifications, but full-time positions typically involve more extensive training and consistent employment.

What does a full time FDA tobacco inspector do?

A Full Time FDA Tobacco Inspector is responsible for enforcing federal regulations related to the manufacturing, distribution, and marketing of tobacco products. Their duties include inspecting retail stores, wholesalers, and manufacturers to ensure compliance with the Family Smoking Prevention and Tobacco Control Act. They collect samples, document violations, educate stakeholders about regulations, and may issue warning letters or fines. These inspectors play a crucial role in protecting public health by reducing youth access to tobacco and ensuring that tobacco products meet safety standards.
What are popular job titles related to Full Time Fda Tobacco Inspector jobs in Riverside, CA? For Full Time Fda Tobacco Inspector jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Full Time Fda Tobacco Inspector jobs in Riverside, CA look for? The top searched job categories for Full Time Fda Tobacco Inspector jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Full Time Fda Tobacco Inspector jobs? Cities near Riverside, CA with the most Full Time Fda Tobacco Inspector job openings:
Full Time Fda Tobacco Inspector jobs near you
Infographic showing various Full Time Fda Tobacco Inspector job openings in Riverside, CA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $57,316 per year, or $27.6 per hour.

Regulatory Affairs Specialist (FDA, DEA )

BaRupOn LLC

Irvine, CA • On-site

$60K - $76K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 4 days ago

Job description

Job Summary

The Regulatory Affairs Specialist (FDA, DEA) will ensure BaRupOn's pharmacy, manufacturing, and healthcare operations meet all applicable regulatory requirements. This position is responsible for preparing submissions, maintaining licenses, coordinating audits, and staying ahead of evolving federal and state regulations related to pharmaceuticals, medical devices, and controlled substances.

Key Responsibilities
  • Prepare and manage FDA submissions (e.g., drug listings, establishment registrations, 503A/503B updates)
  • Oversee and renew DEA registrations, inventory records, and security documentation
  • Maintain state pharmacy, medical device, and wholesale distribution licenses
  • Track regulatory changes affecting compounding, controlled substances, and labeling requirements
  • Support internal audits, site inspections, and responses to 483s or warning letters
  • Coordinate with Quality Assurance on SOP compliance, change controls, and deviation reports
  • Serve as point of contact with federal and state regulatory agencies
  • Document and file compliance records and ensure timely reporting
Qualifications
  • Associate degree in Life Sciences, Regulatory Affairs, or related field (Bachelor's preferred)
  • 2-4 years of regulatory or compliance experience in pharmaceuticals, biotech, or medical devices
  • Working knowledge of FDA regulations (21 CFR Parts 210, 211, 820) and DEA requirements
  • Strong writing, documentation, and organizational skills
  • Familiarity with electronic submission systems, labeling requirements, and drug master files
Preferred Skills
  • Experience in sterile or non-sterile compounding (503A or 503B environments)
  • Knowledge of NABP license portals, MedWatch reporting, or REMS programs
  • Regulatory Affairs Certification (RAC) or DEA compliance training (preferred)
  • Experience responding to FDA inspections, audits, or state pharmacy board requests
Benefits
  • Health, dental, and vision insurance
  • 401(k) with employer match
  • Paid time off and holidays
  • Regulatory training and continuing education support
  • Advancement opportunities into QA/RA leadership roles
Employment Type: FULL_TIME

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