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Fda Inspector Jobs in Anaheim, CA (NOW HIRING)

BiVACOR Inc

QC Inspector

Huntington Beach, CA · On-site

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 ...

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RimePro Inc

Manufacturing Quality Inspector

Hawthorne, CA · On-site

$23 - $34/hr

Verify product conformance to ISO 13485 and FDA regulations * Document inspection results, maintain detailed records, and prepare quality reports * Identify and report quality issues, non ...

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GRIFOLS, S.A.

Quality Inspector

Los Angeles, CA · On-site

$21.35 - $25/hr

Perform visual inspections and dimensional analysis of incoming materials per RMS. * Record ... Understanding of cGMPs, FDA regulations, and industry guidelines, as well as international ...

Grifols

Quality Inspector

Los Angeles, CA · On-site

$21.35 - $25/hr

Perform visual inspections and dimensional analysis of incoming materials per RMS. * Record ... Understanding of cGMPs, FDA regulations, and industry guidelines, as well as international ...

Cosmetix West

SR Quality Assurance Manager

Torrance, CA · On-site

Serve as the Secondary QA contact during FDA inspections and third-party audits; prepare and manage audit responses and CAPA implementation. * Stay current with regulatory changes (e.g., FDA guidance ...

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Abbott

Quality Control Inspector I

Los Angeles, CA · On-site

$16.35 - $32.65/hr

Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies ... Prior medical device component inspection experience preferred. * Experience with optical ...

Abbott

Quality Control Inspector I

Los Angeles, CA · On-site

$16.35 - $32.65/hr

Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies ... Prior medical device component inspection experience preferred. * Experience with optical ...

Del Real Foods

Be Seen First

Quality Control Inspector I

Mira Loma, CA · On-site

$19.30 - $23.71/hr

... inspections on the line(s) including addressing nonessential corrective actions under guidance ... Reports incidents or concerns of compliance issues with USDA & FDA guidelines and regulations.

ZEISS

Quality Control Process Inspector I

Ontario, CA · On-site

$21 - $26/hr

The QC Process Inspector supports Quality Assurance and Quality Control activities in compliance with FDA Quality System Regulations and ISO 13485 standards. This role is responsible for performing ...

ZEISS

Quality Control Process Inspector I

Ontario, CA · On-site

$21 - $26/hr

The QC Process Inspector supports Quality Assurance and Quality Control activities in compliance with FDA Quality System Regulations and ISO 13485 standards. This role is responsible for performing ...

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All JobsFda Inspector JobsFda Inspector Jobs in Anaheim, CA

Fda Inspector information

See Anaheim, CA salary details

$25.6K

$57.5K

$103.6K

How much do fda inspector jobs pay per year?

As of Jul 5, 2026, the average yearly pay for fda inspector in Anaheim, CA is $57,516.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,300.00 and $66,500.00 per year, depending on experience, location, and employer.

How much do FDA drug investigators make?

FDA drug investigators typically earn a salary ranging from $70,000 to $120,000 annually, depending on experience, location, and level of responsibility. They often hold a bachelor's degree in a relevant field and may require specialized training or certifications related to regulatory compliance and inspection procedures.

What types of facilities or products do FDA Inspectors typically 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 are the key skills and qualifications needed to thrive in the Fda Inspector position, and why are they important?

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 type of inspector gets paid the most?

Among FDA inspectors, senior or specialized inspectors, such as those overseeing complex manufacturing facilities or with advanced certifications, tend to earn higher salaries. Experience, certifications, and geographic location also influence pay levels for FDA inspectors. Generally, inspectors with specialized skills or leadership roles earn the most in this field.

Is it hard to get a job at FDA?

Becoming an FDA inspector can be competitive due to strict qualification requirements, including relevant experience, education, and passing civil service exams. Candidates often need a background in science, public health, or regulatory compliance, along with strong attention to detail and communication skills. The hiring process can be lengthy and involves multiple steps such as interviews and background checks.

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 manufacturing. They must pass a written exam and a background check, and often complete on-the-job training or specialized FDA training programs. Certification or licensing is not required but can enhance prospects.

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 are popular job titles related to Fda Inspector jobs in Anaheim, CA? For Fda Inspector jobs in Anaheim, CA, the most frequently searched job titles are:
What job categories do people searching Fda Inspector jobs in Anaheim, CA look for? The top searched job categories for Fda Inspector jobs in Anaheim, CA are:
What cities near Anaheim, CA are hiring for Fda Inspector jobs? Cities near Anaheim, CA with the most Fda Inspector job openings:
Fda Inspector jobs near you

Regulatory Affairs Specialist (FDA, DEA )

BaRupOn LLC

Irvine, CA • On-site

$60K - $76K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 26 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