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Full Time Fda Inspector Jobs in California (NOW HIRING)

Latitude 36 Foods

Sanitation Supervisor

Corona, CA · On-site

$79K - $85K/yr

Corona, California Position Type: Full-time Classification: Exempt Shift: Flexible Salary Range ... inspections is preferred. * HACCP and SQF certifications are preferred. * FDA and/or USDA ...

Latitude 36 Foods

Sanitation Supervisor

Corona, CA

$79K - $85K/yr

Corona, California Position Type: Full-time Classification: Exempt Shift: Flexible Salary Range ... inspections is preferred. * HACCP and SQF certifications are preferred. * FDA and/or USDA ...

ATR International

Quality Engineer

Palo Alto, CA · On-site

$90K - $115K/yr

About the job Full Time Position Onsite in Palo Alto CA Quality Assurance Engineer - Palo Alto, CA ... Develop and improve inspection, testing, and evaluation methods to ensure products meet internal ...

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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.

Associate Regulatory Affairs Manager (San Diego) - Bilingual (Mandarin Speaking)

CorDx

San Diego, CA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 20 days ago

Job description

Who is CorDx?
CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,100 employees across the world, serving millions of users in over 100 countries, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious disease such as COVID-19, pregnancy, drugs of abuse, biomarkers, and more. CorDx is at the cutting edge of technology, artificial intelligence, and data science with the goal of delivering diagnostic solutions to some of the most critical questions in healthcare.
Job Type: Full time
Job Title: Associate Regulatory Affairs Manager
Location: Onsite - San Diego, CA
Position Summary:
The Associate Regulatory Affairs Manager will support the development, review, and submission of regulatory documents for medical device and IVD products. This role will assist in managing regulatory projects, ensuring compliance with FDA, ISO 13485, and other global regulatory requirements. The Associate Manager will work cross-functionally with internal teams and external partners to support product approvals and maintain regulatory compliance throughout the product lifecycle.
Key Responsibilities:
  • Assist in the preparation, review, and submission of regulatory documentation for new products, product changes, and ongoing compliance.
  • Support the regulatory submission process for 510(k), Technical Files, and other regulatory filings.
  • Provide regulatory guidance to cross-functional teams during product development and post-market activities under the direction of senior management.
  • Help track and manage submission timelines, regulatory project plans, and documentation.
  • Stay informed on changes in FDA, ISO 13485, IVDR, and other global regulations, communicating relevant updates to the team.
  • Conduct regulatory assessments for product modifications and assist in defining appropriate submission strategies.
  • Participate in internal and external audits, inspections, and regulatory agency communications as assigned.
  • Contribute to the maintenance of regulatory files and submission records in accordance with internal procedures and regulations.
  • May provide oversight and mentorship to junior staff or specialists on assigned projects.

Requirements
  • Master's degree in Regulatory Affairs, Life Sciences, Engineering, or a related field.
  • 4-6 years supporting or managing 510(k) submissions and regulatory filings.
  • Experience participating in regulatory audits and inspections preferred.
  • Strong organizational, document management, and project coordination skills.
  • Excellent communication, problem-solving, and cross-functional collaboration abilities.
  • Detail-oriented with the ability to manage multiple regulatory projects and priorities.
  • Proficient in Microsoft Office and regulatory document management systems.
  • Ability to work independently and proactively while seeking guidance for complex issues.

Benefits
  • Highly competitive compensation package.
  • Comprehensive medical, dental, and vision insurance.
  • 401(k) plan with generous company contributions.
  • Flexible paid time off (PTO) policy.
  • Additional substantial benefits.

Equal Opportunity Statement: We are an equal opportunity employer committed to inclusion and diversity. We do not discriminate based on race, gender, religion, sexual orientation, age, color, marital status, veteran status, disability status, national origin, or any other protected characteristic.

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