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Full Time Fda Inspector Jobs in California (NOW HIRING)

Nihon Kohden

Quality Systems Manager

Irvine, CA · On-site

$100K - $145K/yr

Facilitate external audits, inspections, and related compliance activities. Ensure the effective ... Solid knowledge of FDA regulations and interpretation of FDA regulations, guidelines and policy ...

Nihon Kohden USA

Quality Systems Manager

Irvine, CA · On-site

$100K - $145K/yr

Facilitate external audits, inspections, and related compliance activities. Ensure the effective ... Solid knowledge of FDA regulations and interpretation of FDA regulations, guidelines and policy ...

Nihon Kohden America

Quality Systems Manager

Irvine, CA · On-site

$100K - $145K/yr

Facilitate external audits, inspections, and related compliance activities. Ensure the effective ... Solid knowledge of FDA regulations and interpretation of FDA regulations, guidelines and policy ...

Prismatik

Regulatory Affairs Specialist, Sr.

Irvine, CA

$84K - $120K/yr

In this role, you'll lead FDA 510(k)/PMA filings, maintain international registrations, support ... Conducts audits and inspections of GMP and non-regulated documentation. * Tracks internal and ...

Fortune Avenue Foods, Inc.

Be Seen First

Quality Control Lead

Ontario, CA · On-site

$30 - $40/hr

We are a USDA / FDA Frozen Food Manufacturer and seeking a Quality Control Lead! The right ... Serves as liaison with USDA inspection personnel whenever needed. * Prepare and lead external ...

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All JobsFda Inspector JobsFull Time Fda Inspector JobsFull Time Fda Inspector Jobs in California

Full Time Fda Inspector information

What does a full time FDA inspector do?

A Full Time FDA Inspector is responsible for ensuring that products regulated by the Food and Drug Administration (FDA)—such as food, drugs, medical devices, and cosmetics—comply with all applicable laws and regulations. They conduct inspections of manufacturing facilities, review processes for safety and quality, collect samples for laboratory analysis, and document their findings. Their work helps protect public health by identifying and addressing potential risks before products reach consumers.

What are the key skills and qualifications needed to thrive as a full time FDA inspector?

To thrive as a Full Time FDA Inspector, you typically need a background in life sciences or a related field, strong analytical abilities, and knowledge of regulatory standards, often supported by a relevant bachelor's degree. Familiarity with inspection software, laboratory equipment, and FDA regulations, such as 21 CFR, is essential. Exceptional attention to detail, critical thinking, and effective communication skills help inspectors conduct thorough evaluations and collaborate with regulated entities. These skills ensure compliance with federal regulations, safeguarding public health and ensuring industry accountability.

What are some common challenges faced by full time FDA inspectors during facility inspections?

Full Time FDA Inspectors often encounter challenges such as navigating complex manufacturing environments, ensuring compliance with evolving regulations, and effectively communicating findings to facility staff. Inspectors must balance thoroughness with efficiency, sometimes facing resistance or misunderstanding from inspected parties. Additionally, staying current on new product types and technologies can require ongoing training and adaptability, making collaboration with colleagues and subject matter experts essential.

What is the difference between Full Time Fda Inspector vs Part Time Fda Inspector?

AspectFull Time Fda InspectorPart Time Fda Inspector
CredentialsTypically requires a bachelor's degree in life sciences or related field, plus FDA inspector certificationSame as full-time, but may have more flexible certification requirements
Work EnvironmentFull-time, on-site inspections at manufacturing facilities, laboratories, and warehousesPart-time, often involves scheduled inspections or follow-ups
Employer & Industry UsageFDA, government agencies, regulated industriesFDA, contractors, or consulting firms

Full Time Fda Inspectors work primarily on-site, conducting regular inspections and ensuring compliance with FDA regulations. Part Time Fda Inspectors perform inspections on a flexible schedule, often supplementing full-time staff. Both roles require similar credentials but differ mainly in hours and scope of work.

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 cities in California are hiring for Full Time Fda Inspector jobs?

Cities in California with the most Full Time Fda Inspector job openings:

Full Time Fda Inspector jobs near you
Infographic showing various Full Time Fda Inspector job openings in California as of August 2026, with employment types broken down into 100% Full Time. Highlights an 95% In-person, and 5% Remote job distribution.

Quality Engineer in Santa Clara, CA (Fulltime, Onsite)

Northern Base

Santa Clara, CA • On-site

$84K - $109K/yr

Full-time

Re-posted 20 days ago

Job description

Senior Quality Engineer
Santa Clara, CA
Fulltime
 
Must Have Technical/Functional Skills
• Strong understanding of Medical Device Quality Systems and regulatory compliance requirements 
• Working knowledge of ISO 13485:2016/2019 and 21 CFR Part 820 (FDA Quality System Regulation) 
• Strong expertise in design transfer activities, including DHF → DMR transition and compliance with FDA 21 CFR 820 & ISO 13485
• Sound knowledge of Medical Device Regulations, including MDD and MDR 
• Proven experience in Non Conformance (NC) management, CAPA processes, and internal/external audits 
• Expertise in Medical Device Risk Management, with the ability to identify both apparent and less obvious risks 
• Practical experience with Application, Process, Design, and System FMEA methodologies 
• Proficient in statistical tools and techniques, including Design of Experiments (DOE) 
• Capable of performing advanced descriptive and non parametric statistical analyses 
• Experienced in leveraging advanced statistical methods for reliability prediction and data driven decision making
 
Roles & Responsibilities
• Lead design transfer and production support activities, ensuring compliance with FDA/ISO 13485 and alignment with manufacturing readiness. 
• Own multiple subassemblies for a surgical robotics platform, ensuring design integrity, quality, and manufacturability. 
• Investigate non-conformances (NCs) using root cause analysis and drive CAPA within the QMS framework. 
• Develop and maintain FMEAs, support risk mitigation, and lead manufacturing issue resolution and qualifications (IQ/OQ/PQ). 
• Identify and implement compliant, alternative solutions to engineering and production challenges while driving continuous improvement.
• Support and maintain Quality Management System (QMS) processes in compliance with regulatory requirements 
• Collaborate with cross functional teams to deliver quality compliant outcomes 
• Interpret and apply medical device regulations and standards to projects and processes 
• Support audits and regulatory inspections, ensuring timely closure of actions