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Fda Inspector Jobs in Davis, CA (NOW HIRING)

Candidates without regulated industry experience (FDA, ISO 13485) will not be considered. Reporting ... Support internal and external audits and maintain inspection readiness. * Partner with Quality to ...

... GMP, and FDA quality standards. Direct silicone injection molding experience is required ... Conduct first-piece inspections and verify dimensional conformance. Troubleshooting & Optimization

Lab Inspection Readiness: Monitor lab conditions to ensure compliance with cGMP and FDA/EMA regulations, maintaining documentation, equipment logs, and records for inspection readiness. Lead ...

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Fda Inspector information

See Davis, CA salary details

$26.5K

$59.4K

$107K

How much do fda inspector jobs pay per year?

As of Jul 28, 2026, the average yearly pay for fda inspector in Davis, CA is $59,382.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,600.00 and $68,600.00 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 Davis, CA? For Fda Inspector jobs in Davis, CA, the most frequently searched job titles are:
What job categories do people searching Fda Inspector jobs in Davis, CA look for? The top searched job categories for Fda Inspector jobs in Davis, CA are:
What cities near Davis, CA are hiring for Fda Inspector jobs? Cities near Davis, CA with the most Fda Inspector job openings:
Infographic showing various Fda Inspector job openings in Davis, CA as of July 2026, with employment types broken down into 84% Full Time, 12% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $59,382 per year, or $28.5 per hour.
QAQC Technician-NDT VT Level II Inspector

QAQC Technician-NDT VT Level II Inspector

FST Technical Services

Vacaville, CA • On-site

$23 - $35/hr

Full-time

Posted 16 days ago


Job description

NDT VT LEVEL II INSPECTOR: FST Technical Services was founded in 1984 to serve the needs of the growing, worldwide Semiconductor/Microelectronics and Life Sciences industries. We began as an independent interface between our clients and their subcontractors to establish build clean installation methods that satisfied internal specifications and conformed to regulatory requirements.
We are growing a new QAQC team for a project based in Vacaville, CA at an exciting pharmaceutical facility build! We are seeking immediate support from experienced NDT VT Level II Inspectors with a history of working a pharmaceutical, semiconductor, data center, or other high-tech facilities.
This opportunity that with excellent pay, strong benefits and a healthy travel/per diem package for travelling resources. Project location is Vacaville, CA.QAQC Technician/NDT VT Level II Inspector
Job Summary
The QAQC Technician and/or ASNT NDT VT Level II Inspector supports pharmaceutical and biotechnology manufacturing facilities by performing Visual Testing (VT) inspections in accordance with ASME, AWS, GMP, and client-specific quality standards. The role focuses on high-purity process piping, clean utilities, pressure systems, and structural components to ensure compliance with regulatory, safety, and quality requirements.Inspection & Testing (Pharma-Specific)
- Perform VT Level II inspections on high-purity stainless steel piping (316L), clean utilities (WFI, PW, Clean Steam), pressure vessels, tanks, skids, and supports.
- Verify weld profiles, surface finish, alignment, fit-up, and workmanship.
- Ensure compliance with project specifications.Documentation, GMP & Validation Support
- Complete GMP-compliant inspection documentation including ITRs, weld logs, and NCRs.
- Ensure documentation is accurate, complete, and audit-ready.
- Participate in system walkdowns, punch list resolution, and audits.Quality & Regulatory Compliance
- Identify defects impacting product quality, cleanability, sterility, or system integrity.
- Adhere strictly to GMP and site quality systems.Preferred Qualifications
- ASNT NDT VT Level II certification from current or previous employer.
- 3-5+ years experience in pharmaceutical or biotech facilities.
- Experience inspecting high-purity stainless steel welds.
- Additional NDT certifications (PT, MT, UT).
- Familiarity with FDA 21 CFR Part 210/211, EU GMP Annex 1, ISPE Baseline Guides.Work Environment
On-site role at pharmaceutical or biotech facilities. May include extended hours, weekends, or travel.
All parties authorized to permanently work in the USA are encouraged to apply. We are unable to sponsor at this time. No third-party candidates considered for this position.
If you are looking for a professional, challenging and stimulating environment and meet the above criteria, APPLY NOW!!!
Hourly pay rate range: $35/HR to $50/HR - based on experience