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Fda Inspector Jobs in California (NOW HIRING)

Quality Control Inspector I

Los Angeles, CA · On-site

$16.35 - $32.65/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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

Quality Control Inspector I

Los Angeles, CA · On-site

$16.35 - $32.65/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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

Quality Control Inspector I

Mira Loma, CA · On-site

$19.30 - $23.71/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Hello! We are looking for a dedicated Quality Control Inspector I to join the family! Del Real ... Reports incidents or concerns of compliance issues with USA & FDA guidelines and regulations.

Manager, Quality Assurance

Fremont, CA · On-site

$165K - $180K/yr

Support external audits and inspections (FDA, notified bodies, customers), including preparation, hosting, and response activities. * Ensure inspection readiness through robust documentation, metrics ...

Head of Regulatory Affairs

San Francisco, CA · On-site

$220K - $280K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Lead preparation and response for FDA inspections * Write and manage Q-Sub (pre-submission) packages Cross-functional execution & alignment * Partner with Clinical Ops to align protocol execution ...

QC Inspector

Santa Ana, CA · On-site

$17 - $21/hr

  • Retirement

  • PTO

We are also FDA registered and ISO 13485 certified. A career with Orchid provides training and ... Collect inspection data and report results. * Maintain accurate documentation at all times during ...

Quality Assurance Inspector I

San Diego, CA · On-site

$18.25/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... 2016, FDA regulations, customer specifications, Argen requirements, and applicable procedures ... Maintain accurate inspection and test records. * Identify and properly label non-conforming ...

... 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 ...

... 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 ...

... 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 ...

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 ...

Quality Inspector

San Diego, CA · On-site

$25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

NOW HIRING QUALITY INSPECTORS FOR A MEDICAL DEVICE COMPANY! Location - Sorrento Valley, CA Shift ... Familiarity with FDA-related requirements in a medical device context. * Proficiency using ...

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 ...

Showing results 21-40

Fda Inspector information

See California salary details

$24.2K

$54.2K

$97.7K

How much do fda inspector jobs pay per year?

As of Aug 13, 2026, the average yearly pay for fda inspector in California is $54,220.00, according to ZipRecruiter salary data. Most workers in this role earn between $38,000.00 and $62,700.00 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 are the most commonly searched types of Fda Inspector jobs in California?

The most popular types of Fda Inspector jobs in California are:

What are popular job titles related to Fda Inspector jobs in California?

For Fda Inspector jobs in California, the most frequently searched job titles are:

What cities in California are hiring for Fda Inspector jobs?

Cities in California with the most Fda Inspector job openings:

Infographic showing various Fda Inspector job openings in California as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $54,220 per year, or $26.1 per hour.

Quality Control Inspector I

Abbott

Los Angeles, CA • On-site

$16.35 - $32.65/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

This job post has expired today. Applications are no longer accepted.


Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 138 frontline employees who took The Breakroom Quiz

178th of 538 rated manufacturers


Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.JOB DESCRIPTION:

A healthy heart is essential to good health. That's why we're committed to advancing treatments for people with cardiovascular disease. As a global leader in Cardiac Rhythm Technologies, our breakthrough medical technologies help restore people's health so they can get back to living their best lives, faster. We focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats.

MAIN PURPOSE OF THE ROLE

The Quality Control Inspector I performs inspection and testing of purchased materials, components and products in accordance with policy and procedures

MAIN RESPONSIBILITIES
  • Performs visual, dimensional and functional inspection and testing according to documented policies and procedures.

  • Records inspection and test data as prescribed by written instructions and procedures.

  • Recommends changes to policies and procedures.

  • Documents non-conformances in Non-Conforming Material Review system.

  • Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.

  • Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.

  • Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.


QUALIFICATIONS
Education
  • High School Diploma / GED or an equivalent combination of education and work experience

Experience/Background
  • Experience - Some - 0-2 year's related work experience.
  • Previous experience in Quality performing inspection.
  • Prior medical device component inspection experience preferred.
  • Experience with optical measurement equipment, hand tools, gages, pressure and force gage testing.
  • Training in blueprint reading and experience with inspection sampling techniques.
  • Knowledge of FDA, GMP, ISO 13485.
  • Good communication and computer skills, including Microsoft Word and Excel.
  • ASQ CMI certification preferred.
  • Ability to work in a highly matrixed and geographically diverse business environment.
  • Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
  • Ability to leverage and/or engage others to accomplish projects.
  • Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
  • Multitasks, prioritizes and meets deadlines in timely manner.
  • Strong organizational and follow-up skills, as well as attention to detail.
  • Must be willing to work overtime as required, including weekends
  • Ability to maintain regular and predictable attendance.

WHAT WE OFFER

At Abbott, you can have a good job that can grow into a great career. We offer:

  • Training and career development, with onboarding programs for new employees and tuition assistance

  • Financial securitythrough competitive compensation, incentives and retirement plans

  • Health care and well-being programsincluding medical, dental, vision, wellness and occupational health programs

  • Paid time off

  • 401(k)retirement savings with a generous company match

  • The stability of a companywith a record of strong financial performance and history ofbeing actively involved in local communities

Learn more about our benefits that add real value to your life to help you live fully:www.abbottbenefits.com

Follow your career aspirations to Abbott for diverse opportunities with a company that provides the growth and strength to build your future. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us atwww.abbott.com, on Facebook atwww.facebook.com/Abbottand on Twitter @AbbottNews and @AbbottGlobal.

The base pay for this position is

$16.35 - $32.65/hour

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:Operations QualityDIVISION:CRM Cardiac Rhythm ManagementLOCATION:United States > Sylmar : 15900 Valley View CourtADDITIONAL LOCATIONS:WORK SHIFT:StandardTRAVEL:Yes, 5 % of the TimeMEDICAL SURVEILLANCE:Not ApplicableSIGNIFICANT WORK ACTIVITIES:Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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