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Fda Inspector Jobs in Davis, CA (NOW HIRING)

Department of Food & Agriculture

Branch Chief

Sacramento, CA · On-site

$14K - $16K/mo

... inspections of farms, processors, and manufacturers of single-service dairy containers for compliance with requirements of the United States Food and Drug Administration (FDA) to ensure approval of ...

New

Tekberry

Warehouse Associate

Woodland, CA · On-site

$22 - $25/hr

Performs quality inspections on incoming and outgoing materials and products * Sorts and places ... Experience in FDA regulated environment -sit down and stand up/reach forklift experience

Tekberry

Warehouse Associate

Woodland, CA · On-site

$22 - $25/hr

Performs quality inspections on incoming and outgoing materials and products * Sorts and places ... Experience in FDA regulated environment -sit down and stand up/reach forklift experience

Orca Bio

Specialist, Training - Night Shift

Sacramento, CA · On-site

$68K - $95K/yr

... visual inspection of materials, equipment, and labeling, including distinguishing color-coded ... Strong understanding of cGMP regulations, FDA guidelines, and other relevant quality standards ...

Pacific Coast Producers

QA Supervisor

Woodland, CA · On-site

$70K - $90K/yr

May be asked to assist or stand-in for the Technical Service Manager during customer and/or government driven inspections or audits, such as FDA, USDA, Kosher, and Organic. * Maintain a clean ...

Orca Bio

Senior Manager, Facilities

Sacramento, CA · On-site

Ensure the facility complies with all relevant safety, environmental, and regulatory requirements (e.g., OSHA, GMP, FDA, local building codes). * Participate in regular inspections to identify and ...

Orca Bio

Manager, Facilities

Sacramento, CA · On-site

$80K - $120K/yr

Ensure the facility complies with all relevant safety, environmental, and regulatory requirements (e.g., OSHA, GMP, FDA, local building codes). * Participate in regular inspections to identify and ...

Orca Bio

Senior Manager, Facilities

Sacramento, CA

$125K - $165K/yr

Ensure the facility complies with all relevant safety, environmental, and regulatory requirements (e.g., OSHA, GMP, FDA, local building codes). * Participate in regular inspections to identify and ...

Orca Bio

Senior Manager, Facilities

Sacramento, CA · On-site

$125K - $165K/yr

Ensure the facility complies with all relevant safety, environmental, and regulatory requirements (e.g., OSHA, GMP, FDA, local building codes). * Participate in regular inspections to identify and ...

Keurig Dr Pepper

Warehouse Supervisor

Sacramento, CA · On-site

$70K - $73K/yr

... FDA). * Ensure all equipment, including but not limited to forklifts, pallet jacks, and fleet trucks, is properly maintained and inspection practices are followed. Total Rewards: * $70,340 - $73,000 ...

Orca Bio

Manager, Facilities

Sacramento, CA

Ensure the facility complies with all relevant safety, environmental, and regulatory requirements (e.g., OSHA, GMP, FDA, local building codes). * Participate in regular inspections to identify and ...

Orca Bio

Manager, Facilities

Sacramento, CA

$80K - $120K/yr

Ensure the facility complies with all relevant safety, environmental, and regulatory requirements (e.g., OSHA, GMP, FDA, local building codes). * Participate in regular inspections to identify and ...

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All JobsFda Inspector JobsFda Inspector Jobs in Davis, CA

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 6, 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:
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Fda Inspector jobs near you
In-Process Quality Assurance (QA) Specialist

In-Process Quality Assurance (QA) Specialist

Yoh, A Day & Zimmermann Company

Sacramento, CA

$80K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 23 days ago

Job description

About the Job:
A rapidly growing specialty pharmaceutical company is seeking a motivated and detail-oriented In-Process Quality Assurance (QA) Specialist to support manufacturing operations in a regulated pharmaceutical environment. In this role, you will serve as a key quality partner on the production floor, ensuring products are manufactured in compliance with cGMP requirements, internal procedures, and regulatory standards.
Key Responsibilities:
  • Provide real-time QA oversight of manufacturing and packaging operations.
  • Perform line clearances, in-process inspections, and quality verification activities.
  • Review batch records, logbooks, and production documentation for accuracy and compliance.
  • Support investigations related to deviations, non-conformances, and quality events.
  • Assist with CAPA activities, root cause analysis, and continuous improvement initiatives.
  • Review and support updates to manufacturing procedures, controlled documents, and batch records.
  • Participate in GMP walkthroughs, audit readiness activities, and inspection support.
  • Partner with Manufacturing, Engineering, Validation, Supply Chain, and Quality teams to resolve issues and drive compliance.
  • Support product disposition and quality review processes.
  • Promote a strong culture of quality, compliance, and operational excellence.

Education and Experience:
  • Bachelor's degree in Life Sciences, Chemistry, Engineering, or a related discipline, or combination of education and experience in sterile GMP manufacturing.
  • 0-3 years of experience in pharmaceutical, biotechnology, or other regulated manufacturing environments.
  • Understanding of cGMP principles and FDA regulatory requirements.
  • Strong attention to detail and organizational skills.
  • Excellent communication and documentation abilities.
  • Ability to work independently and collaboratively in a fast-paced manufacturing environment.
  • Experience with deviation investigations, CAPA, change control, or quality systems is a plus.
  • Familiarity with electronic quality management systems (eQMS), ERP systems, LIMS, or similar platforms is preferred.
  • Proficiency with Microsoft Office applications.
Benefits
  • Competitive pay.
  • medical, dental, and vision
  • Paid time off
  • 401 (k)

Estimated Min Rate: $56000.00
Estimated Max Rate: $80000.00
What’s In It for You?
We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include:
  • Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)
  • Health Savings Account (HSA) (for employees working 20+ hours per week)
  • Life & Disability Insurance (for employees working 20+ hours per week)
  • MetLife Voluntary Benefits
  • Employee Assistance Program (EAP)
  • 401K Retirement Savings Plan
  • Direct Deposit & weekly epayroll
  • Referral Bonus Programs
  • Certification and training opportunities

Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Visit https://www.yoh.com/applicants-with-disabilities to contact us if you are an individual with a disability and require accommodation in the application process.
For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice: https://www.yoh.com/privacy-notice

Company Description

Yoh delivers expertise, methodology, and momentum to keep work moving forward. From strategy to execution, we deliver bold ideas and big results through consulting, staffing, and enterprise solutions. Nearly a century after our founding, Yoh remains STEM-centered, collaborative, and committed to client success. Yoh is a proud member of the Day & Zimmermann family of companies. Visit us at https://www.yoh.com/