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Full Time Fda Inspector Jobs in California (NOW HIRING)

Jensen Meat

QA Supervisor

Riverside, CA · On-site

$32 - $35/hr

Job Type Full-time Description FLSA Status: Full-Time / Non-Exempt Location: Jensen Meat Company ... FDA regulated food manufacturing environment. (Dual inspection experience preferred) • Strong ...

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

$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 ...

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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 California? The most popular types of Fda Inspector jobs in California are:
What cities in California are hiring for Full Time Fda Inspector jobs? Cities in California 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 California as of August 2026, with employment types broken down into 100% Full Time. Highlights an 97% In-person, and 3% Remote job distribution.

Regulatory Affairs Specialist (FDA, DEA )

BaRupOn LLC

Irvine, CA

$60K - $76K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 29 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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