... FDA/ISO 13485 environment. Need 2-5 years of experience using calipers, micrometers, and gages, strong vision/optical inspection, operating CMM skills, solid blueprint reading capability, and ...
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... FDA/ISO 13485 environment. Need 2-5 years of experience using calipers, micrometers, and gages, strong vision/optical inspection, operating CMM skills, solid blueprint reading capability, and ...
Quick apply
... FDA/ISO 13485 environment. Need 2-5 years of experience using calipers, micrometers, and gages, strong vision/optical inspection, operating CMM skills, solid blueprint reading capability, and ...
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 ...
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 ...
... FDA/ISO 13485 environment. Need 2-5 years of experience using calipers, micrometers, and gages, strong vision/optical inspection, operating CMM skills, solid blueprint reading capability, and ...
Quick apply
... FDA/ISO 13485 environment. Need 2-5 years of experience using calipers, micrometers, and gages, strong vision/optical inspection, operating CMM skills, solid blueprint reading capability, and ...
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 ...
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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 ...
San Francisco, CA · On-site
$220K - $280K/yr
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 ...
San Francisco, CA · On-site
$220K - $280K/yr
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 ...
Fremont, CA · On-site
$165K - $180K/yr
Support internal audits, notified body audits, customer audits, FDA inspections, and supplier-related regulatory activities. * Support Management Review through supplier quality performance reporting ...
Quick apply
Fremont, CA · On-site
$165K - $180K/yr
Support internal audits, notified body audits, customer audits, FDA inspections, and supplier-related regulatory activities. * Support Management Review through supplier quality performance reporting ...
Fremont, CA · On-site
$165K - $180K/yr
Support internal audits, notified body audits, customer audits, FDA inspections, and supplier-related regulatory activities. * Support Management Review through supplier quality performance reporting ...
Quick apply
Fremont, CA · On-site
$165K - $180K/yr
Support internal audits, notified body audits, customer audits, FDA inspections, and supplier-related regulatory activities. * Support Management Review through supplier quality performance reporting ...
Fremont, CA · On-site
$27.78/hr
Required Skills: · High School Diploma or GED is required. · Minimum 1 year or more work experience in GMP/cGMP/FDA regulated industry. · Experience as a Quality Inspector, Inspection Technician ...
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Fremont, CA · On-site
$27.78/hr
Required Skills: · High School Diploma or GED is required. · Minimum 1 year or more work experience in GMP/cGMP/FDA regulated industry. · Experience as a Quality Inspector, Inspection Technician ...
Pleasanton, CA · On-site
$55 - $57/hr
Support major Quality System investigations, including CAPAs, Health Hazard Evaluations (HHEs), and internal and external audits, including FDA inspections. Risk Management * Lead risk analysis ...
Pleasanton, CA · On-site
$55 - $57/hr
Support major Quality System investigations, including CAPAs, Health Hazard Evaluations (HHEs), and internal and external audits, including FDA inspections. Risk Management * Lead risk analysis ...
$21 - $28.75/hr
We operate cGMP peptide production facilities in Menlo Park, CA, and passed an FDA inspection in 2017 that recommended us for commercial drug substance manufacturing. In 2023, we added cGMP clinical ...
$21 - $28.75/hr
We operate cGMP peptide production facilities in Menlo Park, CA, and passed an FDA inspection in 2017 that recommended us for commercial drug substance manufacturing. In 2023, we added cGMP clinical ...
San Francisco, CA · On-site
$175K - $235K/yr
Experience supporting FDA inspections, audits, or regulatory compliance activities * Background in Lean Manufacturing or Six Sigma methodologies applied to low-volume, high-mix production ...
San Francisco, CA · On-site
$175K - $235K/yr
Experience supporting FDA inspections, audits, or regulatory compliance activities * Background in Lean Manufacturing or Six Sigma methodologies applied to low-volume, high-mix production ...
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 ...
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 ...
Milpitas, CA · On-site
$20.50 - $28.25/hr
We operate cGMP peptide production facilities in Menlo Park, CA, and passed an FDA inspection in 2017 that recommended us for commercial drug substance manufacturing. In 2023, we added cGMP clinical ...
Quick apply
Milpitas, CA · On-site
$20.50 - $28.25/hr
We operate cGMP peptide production facilities in Menlo Park, CA, and passed an FDA inspection in 2017 that recommended us for commercial drug substance manufacturing. In 2023, we added cGMP clinical ...
Milpitas, CA · On-site
$20.50 - $28.25/hr
We operate cGMP peptide production facilities in Menlo Park, CA, and passed an FDA inspection in 2017 that recommended us for commercial drug substance manufacturing. In 2023, we added cGMP clinical ...
Milpitas, CA · On-site
$20.50 - $28.25/hr
We operate cGMP peptide production facilities in Menlo Park, CA, and passed an FDA inspection in 2017 that recommended us for commercial drug substance manufacturing. In 2023, we added cGMP clinical ...
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 ...
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 ...
Receive, unpack, and inspect returned customer products. * Investigate product complaints using ... Follow FDA regulations, SOPs, and quality system requirements. * Support product handling ...
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Receive, unpack, and inspect returned customer products. * Investigate product complaints using ... Follow FDA regulations, SOPs, and quality system requirements. * Support product handling ...
Emeryville, CA · On-site
$220K - $246K/yr
Our FDA cleared, industry leading products are used by hundreds of thousands of clinicians on ... inspections, and ongoing correspondence * Partner with cross-functional teams (R&D, Clinical ...
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Emeryville, CA · On-site
$220K - $246K/yr
Our FDA cleared, industry leading products are used by hundreds of thousands of clinicians on ... inspections, and ongoing correspondence * Partner with cross-functional teams (R&D, Clinical ...
Emeryville, CA · On-site
$173K - $229K/yr
Our FDA cleared, industry leading products are used by hundreds of thousands of clinicians on ... inspections, and ongoing correspondence * Partner with cross-functional teams (R&D, Clinical ...
Emeryville, CA · On-site
$173K - $229K/yr
Our FDA cleared, industry leading products are used by hundreds of thousands of clinicians on ... inspections, and ongoing correspondence * Partner with cross-functional teams (R&D, Clinical ...
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 ...
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 ...
$173K - $229K/yr
Our FDA cleared, industry leading products are used by hundreds of thousands of clinicians on ... inspections, and ongoing correspondence * Partner with cross-functional teams (R&D, Clinical ...
$173K - $229K/yr
Our FDA cleared, industry leading products are used by hundreds of thousands of clinicians on ... inspections, and ongoing correspondence * Partner with cross-functional teams (R&D, Clinical ...
$26.8K - $34.2K
3% of jobs
$34.2K - $41.6K
16% of jobs
$43.5K is the 25th percentile. Wages below this are outliers.
$41.6K - $49.1K
23% of jobs
The median wage is $51.3K / yr.
$49.1K - $56.5K
27% of jobs
$61.2K is the 75th percentile. Wages above this are outliers.
$56.5K - $63.9K
10% of jobs
$63.9K - $71.3K
4% of jobs
$71.3K - $78.7K
5% of jobs
$78.7K - $86.1K
2% of jobs
$86.1K - $93.5K
2% of jobs
$93.5K - $101K
2% of jobs
$101K - $108.4K
5% of jobs
$26.8K
$60.1K
$108.4K
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.
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.
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.

Contractor
Posted 10 days ago
Role: Inspector II
Location: San Ramon, CA - 94583
Duration: 6 Months
Shift Timings: 1:30 PM to 10 PM
Job Description:
Position Summary: Performs inspection and testing of purchased materials, components and products in accordance with policy and procedures.
Essential Functions:
Must be able to read and comprehend drawings and basic GD&T.
Performs visual, dimensional and functional inspection and testing according to documented policies and procedures.
Experience with microscopes and inspecting up to 30x magnification.
Records inspection and test data as prescribed by written instructions and procedures.
Operates all associated test and measurement equipment as instructed and as documented in procedures.
Recommends changes to policies and procedures.
Documents non-conformances in Non-Conforming Material Review system. Support all Divisional initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
We’re hiring an Incoming/Receiving Quality Inspector (Inspector II) responsible for visual inspection under 30× magnification, dimensional measurements , and support for FAI and GR&R activities in a regulated FDA/ISO 13485 environment.
Need 2–5 years of experience using calipers, micrometers, and gages, strong vision/optical inspection, operating CMM skills, solid blueprint reading capability, and excellent documentation practices.
Sourced by ZipRecruiter
51 - 200 Employees
Iselin, NJ, US
2018