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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 ...

Inquis Medical, Inc.

Sr. Quality Engineer

Menlo Park, CA · On-site

$104K - $141K/yr

Lead and participate in: internal audits, supplier audits, FDA Inspections, ISO Certification Audits, and Notified Body Audits. * Support responses to audit observations and implementation of ...

New

Inquis Medical, Inc.

Sr. Quality Engineer

San Francisco, CA · On-site

$104K - $141K/yr

Lead and participate in: internal audits, supplier audits, FDA Inspections, ISO Certification Audits, and Notified Body Audits. * Support responses to audit observations and implementation of ...

New

Adialante LLC

Senior Quality Engineer

Menlo Park, CA · On-site

$150 - $210/hr

Direct experience preparing for or leading FDA inspections, MDSAP audits, or ISO 13485 audits, and communicating with regulatory authorities * Familiarity with international regulatory frameworks

New

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 · 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*

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 · On-site

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.

Grifols

Product Inspector (2nd shift)

Clayton, CA · On-site

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 ...

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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 21, 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.

What are popular job titles related to Fda Inspector jobs in Oakland, CA?

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

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The top searched job categories for Fda Inspector jobs in Oakland, CA are:

What cities near Oakland, CA are hiring for Fda Inspector jobs?

Cities near Oakland, CA with the most Fda Inspector job openings:

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 Inspector

Rani Therapeutics

Fremont, CA • On-site

$37 - $42/hr

Full-time

Re-posted 10 days ago

Job description

GENERAL INFORMATION
Position Title:
Quality Inspector (II, III, or Senior)
Department:
Quality Assurance
Reports to:
Quality Engineering
Purpose of the Job
This Quality Inspector position will report to Quality Engineering. Main responsibilities include performing incoming inspections of materials/parts/products and reviewing and approval of manufacturing batch records and inspection records. This position will require to perform disposition of materials/parts/products. As a Quality Inspector, you will also support Quality Engineering with other Quality Management System (QMS) activities, such as assisting with environmental monitoring and quality metrics.
Major Duties and Responsibilities
  • Interpret drawings and specification documents.
  • Perform incoming inspection of materials/components/subassemblies/finished products following standard operating procedures and using standard inspection tools, including the MicroVu and Keyence.
  • Determine inspection sample size based on procedures, specifications, and standards.
  • Help develop inspection methods, including automated inspection programs using the MicroVu and Keyence.
  • Review/approve executed batch records for manufacturing and inspection records in accordance to QMS procedures and Good Documentation Practices.
  • Approve/perform final disposition of materials/components/subassemblies/finished products.
  • Assign and apply expiration dating labels to materials/parts/products, as per specifications/quality procedures.
  • Initiate Non-Conformance Material Reports (NCMRs) and deviations when discrepancies are observed during inspections and record review process. Report discrepancies and issues to QA Engineering and affected function(s).
  • Maintain materials in Quarantine (pending disposition) and MRB (under NCMR and deviations) in order.
  • Maintain accurate records as per Document Control procedures.
  • Support training of IQC personnel.
  • Assist with performing environmental monitoring of Controlled Environment Rooms (CERs), as needed.
  • Support Quality in the collection of quality metrics data.
  • Interact closely with different functions of the organization.
Education and/or Job Experience
  • 2-5 years of experience performing inspections and reviews/approvals of manufacturing batch records/inspection records
  • Government Regulated Environment experience such as FDA and ISO 13485
  • Must have adequate computer experience (knowledge of Microsoft Word, Excel)
  • Experience working in a cGMP environment
Skills and Specifications
  • Attention to detail and organizational skills
  • Good interpersonal and communication skills
  • Ability to work as a part of a team and promote a team environment

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