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Fda Inspector Jobs in Long Beach, CA (NOW HIRING)

BaRupOn LLC

Regulatory Affairs Specialist (FDA, DEA )

Irvine, CA · On-site

$60K - $76K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Support internal audits, site inspections, and responses to 483s or warning letters * Coordinate ... Working knowledge of FDA regulations (21 CFR Parts 210, 211, 820) and DEA requirements * Strong ...

BaRupOn LLC

Regulatory Affairs Specialist (FDA, DEA )

Irvine, CA · On-site

$60K - $76K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Support internal audits, site inspections, and responses to 483s or warning letters * Coordinate ... Working knowledge of FDA regulations (21 CFR Parts 210, 211, 820) and DEA requirements * Strong ...

Barupon LLC

Regulatory Affairs Specialist (FDA, DEA )

Irvine, CA · On-site

$60K - $76K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Support internal audits, site inspections, and responses to 483s or warning letters * Coordinate ... Working knowledge of FDA regulations (21 CFR Parts 210, 211, 820) and DEA requirements * Strong ...

BiVACOR Inc

QC Inspector

Huntington Beach, CA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

About the Role This is a high-impact, hands-on quality role in an FDA-regulated, Class III medical ... Key Responsibilities * Inspect PCBAs, wire harnesses, and electronic assemblies * Conduct ...

BiVACOR Inc

QC Inspector

Huntington Beach, CA · On-site

$22 - $35/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

About the Role This is a high-impact, hands-on quality role in an FDA-regulated, Class III medical ... Key Responsibilities * Inspect PCBAs, wire harnesses, and electronic assemblies * Conduct ...

KORE1 Technologies

Quality Control Inspector

Irvine, CA · On-site

$26 - $28/hr

... FDA 21 CFR Part 820) is preferred. * Experience with incoming or in-process inspection, able to ... read and understand Engineering Drawings and Part Specifications. * Experience participating in ...

KORE1 Technologies

Quality Control Inspector

Irvine, CA · On-site

... FDA 21 CFR Part 820) is preferred. * Experience with incoming or in-process inspection, able to ... read and understand Engineering Drawings and Part Specifications. * Experience participating in ...

KORE1 Technologies

Quality Control Inspector

Irvine, CA

$26 - $28/hr

... FDA 21 CFR Part 820) is preferred. * Experience with incoming or in-process inspection, able to ... read and understand Engineering Drawings and Part Specifications. * Experience participating in ...

Astrix Inc

QA Inspector- Cosmetics (2nd & 3rd)

Pomona, CA · On-site

$20 - $25/hr

Ensure that all personal care products comply with industry regulations and standards, such as FDA ... Proven experience as a QC Inspector in a GMP regulated environment. * Strong attention to detail ...

B. Braun Group

Inspector

Irvine, CA · On-site

$21.84/hr

  • Medical

  • Retirement

Inspector Company: B. Braun US Pharmaceutical Manufacturing LLC Job Posting Location: Irvine ... Perform production related tasks in an FDA and cGMP regulated environment * Perform routine ...

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All JobsFda Inspector JobsFda Inspector Jobs in Long Beach, CA

Fda Inspector information

See Long Beach, CA salary details

$25.8K

$57.8K

$104.1K

How much do fda inspector jobs pay per year?

As of Aug 15, 2026, the average yearly pay for fda inspector in Long Beach, CA is $57,767.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,500.00 and $66,800.00 per year, depending on experience, location, and employer.

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.

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.

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 the FDA's specialized training program and often require a background check and security clearance; some positions may also require state licensure or certifications. Strong attention to detail, knowledge of regulatory standards, and good communication skills are essential for the role.

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 job categories do people searching Fda Inspector jobs in Long Beach, CA look for?

The top searched job categories for Fda Inspector jobs in Long Beach, CA are:

What cities near Long Beach, CA are hiring for Fda Inspector jobs?

Cities near Long Beach, CA with the most Fda Inspector job openings:

Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in Long Beach, CA as of August 2026, with employment types broken down into 79% Full Time, 9% Part Time, 11% Contract, and 1% Nights. Highlights an 97% Physical, and 3% Remote job distribution, with an average salary of $57,767 per year, or $27.8 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 7 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)
  • 24 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