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Fda Inspector Jobs in Oakland, CA (NOW HIRING)

Rani Therapeutics

Quality Inspector

Fremont, CA · On-site

$37 - $42/hr

Quality Inspector (II, III, or Senior) Department: Quality Assurance Reports to: Quality ... Government Regulated Environment experience such as FDA and ISO 13485 * Must have adequate computer ...

THINK Surgical, Inc.

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 ...

Noah Medical

Sr. RA Specialist

San Jose, CA · Hybrid

Committed to exceeding FDA and international regulatory standards, we take initiative, optimize ... Audits & Inspections * Support internal audits, external audits, notified body assessments, and ...

Noah Medical

Sr. RA Specialist

San Jose, CA · On-site

Committed to exceeding FDA and international regulatory standards, we take initiative, optimize ... Audits & Inspections * Support internal audits, external audits, notified body assessments, and ...

Penumbra

Product Stewardship Specialist I

Alameda, CA

$72K - $94K/yr

Responsible for supporting management during FDA inspections and/or other notified body audits * * Interface with other internal departments on quality-related issues. Review supplier related data*

Penumbra

Product Stewardship Specialist I

Alameda, CA · On-site

$72K - $94K/yr

Responsible for supporting management during FDA inspections and/or other notified body audits * * Interface with other internal departments on quality-related issues. Review supplier related data*

Grifols

Product Inspector (2nd shift)

Clayton, CA

A visual inspection of plasma units is also performed, removing any units which are unacceptable (e ... Two years' experience in Manufacturing, Pharmaceutical or other FDA licensed Industry is desirable.

Tempus AI

Senior Quality Engineer

Redwood City, CA · On-site

$108K - $146K/yr

... external inspections and regulatory and customer audits. • Provide CSV guidance, coaching ... FDA regulated domain (e.g. medical device, pharma, biotech) • 3+ years experience in Computer ...

Grifols

Product Inspector (2nd shift)

Clayton, CA

A visual inspection of plasma units is also performed, removing any units which are unacceptable (e ... Two years' experience in Manufacturing, Pharmaceutical or other FDA licensed Industry is desirable.

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All JobsFda Inspector JobsFda Inspector Jobs in Oakland, CA

Fda Inspector information

See Oakland, CA salary details

$28.1K

$63.1K

$113.7K

How much do fda inspector jobs pay per year?

As of Aug 18, 2026, the average yearly pay for fda inspector in Oakland, CA is $63,096.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,200.00 and $72,900.00 per year, depending on experience, location, and employer.

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 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.

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.

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 a written exam and a background check, and often undergo specialized training at the FDA's training center. Certification or licensing is not required but can enhance prospects in the field.

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Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in Oakland, CA as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 17% Part Time, 2% Contract, and 1% Nights. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $63,096 per year, or $30.3 per hour.

Quality Control Inspector III

Confluent Medical Technologies

Fremont, CA • On-site

$22.75 - $37.75/hr

Full-time

Posted 10 days ago

Job description

Salary Range:

$22.75 - $37.75

Job Description:

Confluent Medical Technologies is dedicated to working collaboratively with our customers, taking their projects from rapid prototype into high volume production.Our unparalleled technicalexpertise, proven experience and partnership with our clientshasallowed us to perfect the process necessary to deliver world-class medical devices through innovative material science, engineering, and manufacturing. Our primary capabilitiesinclude:Nitinol components, balloon expandable stents and balloon catheters, delivery systems, biomedical textiles, access kits, and guidewires. We take pride in our position as the leader in the medical technology space and are driven by a passion to create products that our clients have envisioned for their customers.

We arelooking for aQuality Control Inspector IIIto join ourFremont, CAteam for a 8:30am-5:00pm shift.As a uniquely qualified candidate, you will:

  • Performs final inspection of raw material per procedures

  • Performs in-process and final inspection for medical components/material per procedures to certify quality and adherence to specifications

  • Performs inspections and final checks

  • Recordsinspection and test results perprocedures.

  • Data entry in database asrequired. Working knowledge of Excel preferred.

  • Position interacts with various development departments and requiresindividualto be supportive, cooperative and an effective communicator.

  • Complies withall Quality System policies and procedures.

  • Performs othertasks asassigned by Supervisor/Manager.

  • Coordinate and control that product and product process changes documented through the product/process change system arevalidatedaccording to the established requirements per Design and Change Control systems.

  • Supports OC training / filing of employee training records.

  • Supportappropriate partiesduring internal and external customer and regulatory audits.

Education and Experience:

  • High School diplomawith minimum7years' experience inmedical device or FDA regulated industry.

  • Ability to read engineering drawings and understand inspection requirements.

  • Good written and verbal communication skills.

  • Experience with a medical device firm (orsub-contractor) with clean room environment inspection preferred.

  • Experience with inspection, including measurement tools, interpreting engineering drawings preferred.

  • Knowledge of International Standards (ISO) and FDA Regulations for Medical Industry

  • Knowledge of good manufacturing principles (GMP& GDP)

  • Attention to detail, professional attitude, team player.

We regret that we are unable to sponsor employment visas or consider individuals on time-limited visa status for this position.

Confluent Medical Technologies is an equal opportunity employer.

Only qualified candidates will be contacted.

Apply