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Quality Assurance Incoming Inspector Jobs in Carson, CA

mercury

Int Quality Assurance Tech

Torrance, CA · On-site

Performing Quality Assurance related tasks in support of engineering and operations. incoming, in-process and final inspection.Reviewing supporting data, documentation and generating inspection ...

Robinson Pharma

QA Inspector I - 1st shift

Santa Ana, CA · On-site

$18 - $23/hr

The QA Inspector must be highly detailed, have good communication (oral and written), and have good computer skills. This individual monitors and supports operations and enforces cGMPs and SOPs.

BioPhase Solutions

QA Specialist

Anaheim, CA

$25 - $35/hr

Providing assistance during cGMP compliance inspections of the facility by clients, the FDA and/or ... Supporting QA management in gathering data necessary for tracking quality metrics. * Maintaining ...

The Patriot Group

QA/QC Engineer

Huntington Beach, CA

$90K - $135K/yr

... incoming, in-process, and final inspections to ensure components and assemblies meet specifications ● Review, update, and create assembly procedures, acceptance test procedures, SOPs, schematics ...

The Patriot Group, Inc

QA/QC Engineer

Huntington Beach, CA · On-site

$90K - $135K/yr

... incoming, in-process, and final inspections to ensure components and assemblies meet specifications • Review, update, and create assembly procedures, acceptance test procedures, SOPs, schematics ...

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All JobsQuality Assurance Incoming Inspector JobsQuality Assurance Incoming Inspector Jobs in Carson, CA

Quality Assurance Incoming Inspector information

See Carson, CA salary details

$14

$23

$40

How much do quality assurance incoming inspector jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for quality assurance incoming inspector in Carson, CA is $23.88, according to ZipRecruiter salary data. Most workers in this role earn between $18.37 and $26.92 per hour, depending on experience, location, and employer.

What is the role of incoming Quality Assurance Incoming Inspector?

An incoming Quality Assurance Inspector is responsible for inspecting and testing raw materials, components, or finished products upon arrival to ensure they meet quality standards and specifications. They document inspection results, identify defects, and collaborate with suppliers and production teams to address quality issues, often using tools like calipers, gauges, or measurement devices. This role helps prevent defective items from progressing through the manufacturing process, supporting overall product quality and compliance.

What are the key skills and qualifications needed to thrive as a quality assurance incoming inspector?

To thrive as a Quality Assurance Incoming Inspector, you need strong attention to detail, knowledge of quality control standards, and often a background in manufacturing or a related technical field. Familiarity with measurement tools (calipers, micrometers), inspection software, and sometimes certifications such as ASQ Certified Quality Inspector are typically required. Excellent documentation skills, problem-solving abilities, and clear communication are essential soft skills in this role. These skills and qualifications ensure accurate verification of incoming materials, support compliance with quality standards, and help prevent defects in the manufacturing process.

How much do quality assurance incoming inspectors earn?

Quality assurance incoming inspectors typically earn between $35,000 and $55,000 annually, depending on experience, location, and industry. Entry-level inspectors may start at lower wages, while experienced professionals with certifications can earn higher salaries. The role often requires attention to detail and familiarity with inspection tools and standards.

What does a quality assurance incoming inspector do?

A Quality Assurance Incoming Inspector is responsible for inspecting and verifying the quality of raw materials, components, or products as they arrive from suppliers before they are used in the manufacturing process. They check for defects, compliance with specifications, and adherence to quality standards. Their role helps ensure that only materials that meet company criteria are used, which helps prevent production issues and maintains product quality. Inspectors typically use measuring tools, review documentation, and may create reports on their findings.

What are some typical challenges faced by quality assurance incoming inspectors when evaluating new materials or components?

Quality Assurance Incoming Inspectors often encounter challenges such as identifying subtle defects in large batches, understanding complex technical specifications, and keeping up with evolving quality standards. They must work closely with suppliers and internal teams to resolve discrepancies and ensure that all incoming materials meet strict requirements. Managing time effectively to inspect high volumes without sacrificing accuracy is also a critical aspect of the role.

What is the difference between Quality Assurance Incoming Inspector vs Quality Control Inspector?

AspectQuality Assurance Incoming InspectorQuality Control Inspector
Primary FocusPrevent defects by inspecting incoming materialsIdentify defects in finished products or during production
Work EnvironmentReceiving areas, supplier sites, warehousesProduction lines, testing labs, final inspection areas
CertificationsISO 9001, ASQ certifications often preferredQuality control certifications, sometimes ASQ Certified Quality Inspector
Employer & Industry UsageManufacturing, aerospace, automotive, electronicsManufacturing, consumer goods, electronics, automotive

While both roles focus on quality, the Quality Assurance Incoming Inspector emphasizes preventing defects by inspecting incoming materials, whereas the Quality Control Inspector concentrates on identifying defects during or after production. Understanding these differences helps employers and job seekers target the right skills and certifications for each position.

What are popular job titles related to Quality Assurance Incoming Inspector jobs in Carson, CA? For Quality Assurance Incoming Inspector jobs in Carson, CA, the most frequently searched job titles are:
What cities near Carson, CA are hiring for Quality Assurance Incoming Inspector jobs? Cities near Carson, CA with the most Quality Assurance Incoming Inspector job openings:
Quality Assurance Incoming Inspector jobs near you

QA Compliance Specialist

De Silva Brothers & Company and G.P. De Silva Spices Inc.

Pico Rivera, CA

$31 - $37/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago

Job description

QA Compliance Specialist
Location: Pico Rivera, CA (on-site position)
Reports to: Quality Assurance Manager
Scope: Supports both De Silva Brothers amp; Company and GP De Silva Spices, Inc.
Status: Full-time, non-exempt (hourly, overtime eligible)
Pay scale: $31.00 – $37.00 per hour
About the role
We run two food businesses out of one campus. De Silva Brothers amp; Company is an SQF-certified blending and co-packing operation. GP De Silva Spices is a wholesale importer and distributor of dried chiles, spices, herbs, grains and seeds, and serves as FSVP importer of record for product sourced from Mexico, Peru, India, China and Nigeria.
Both run on documentation. Supplier files, customer specifications, controlled SOPs, training records, lab results, audit packets — if the paper isn't right, the product doesn't ship and the audit doesn't pass.
This role owns that paper. You will be the person who knows, at any moment, which supplier certificates are current, which customer portals need updating, which SOPs are due for review, and which lab results are still outstanding. When an auditor, a customer, or the FDA asks for a record, you produce it the same day.
This is a systems and records role, not a floor QA role. Product disposition, CCP decisions, and supplier approval authority rest with the QA Manager. You build and defend the documentation those decisions stand on.
What you'll ownSupplier documentation and approval records
  • Request, collect, review for completeness, and file all required supplier documents for both entities
  • Track expiration dates and drive renewals on a standing cadence (60- and 30-day notice), escalating non-responsive suppliers to QA and Purchasing
  • Maintain the Approved Supplier List for both entities and keep it reconciled with purchasing records
  • Manage the full document set: supplier questionnaires, GFSI certificates (SQF, BRCGS, FSSC 22000) and audit reports, continuing guaranties and letters of guarantee, allergen and sesame declarations, specifications, COAs (micro, heavy metals, mycotoxin, pesticide), country-of-origin and traceability records, Prop 65 statements, kosher and organic certifications, FDA registration numbers, insurance certificates and W-9s
  • Verify that incoming lots arrive with required documentation before release; flag gaps to QA and Receiving
  • Maintain FSVP supporting records under the direction of the QA Manager
Customer and co-pack documentation
  • Complete customer specification forms, quality questionnaires, and vendor qualification packets
  • Maintain company profiles and document uploads in customer compliance portals (ReposiTrak, TraceGains, FoodLogiQ and similar)
  • Issue company letters of guarantee, allergen statements, Prop 65 statements, and claim documentation to customers
  • Serve as the first point of contact for routine customer documentation requests
Internal document control
  • Administer the controlled document system: version control, issuance, revision history, and retrieval of obsolete copies
  • Maintain the annual SOP and policy review calendar and prompt document owners ahead of due dates
  • Administer training records — GMP, food safety, allergen, and new-hire onboarding — and track refresher due dates
Lab and testing coordination
  • Schedule third-party lab submissions and maintain sample chain-of-custody records
  • Track results against specification and escalate out-of-spec findings immediately to the QA Manager
  • Maintain the testing calendar and environmental monitoring records
Audit, certification, and program administration
  • Prepare documentation packets and coordinate logistics for SQF audits, customer audits, kosher inspections, and FDA inspections
  • Schedule internal audits and track findings and corrective actions to closure
  • Administer mock recall and traceability exercises and compile the results
  • Maintain the CAPA log, supplier nonconformance log, and customer complaint log
  • Manage kosher ingredient submissions and annual certification renewals
Regulatory monitoring
  • Monitor FDA import alerts, refusal reports, and recall notices against the active supplier list and current inventory; escalate hits to QA and Purchasing
What success looks like
  • 90 days: You know both supplier lists cold, have audited every file, and delivered a gap report showing what's missing or expired.
  • 6 months: No expired documents on active suppliers. Renewals go out on schedule without prompting. Customer documentation requests are answered same-day.
  • 12 months: Documentation is a non-issue in the SQF audit. Any record — supplier, customer, training, or lab — can be produced on request within the hour.
Required qualifications
  • 2–4 years in food industry quality assurance, document control, regulatory compliance, or supplier management
  • Working familiarity with HACCP, GMPs, and FSMA, and the ability to learn SQF and FSVP recordkeeping requirements quickly
  • Strong Excel skills (filtering, lookups, tracking logs) and comfort with document management systems and web-based customer portals
  • Exceptional attention to detail and follow-through; able to manage hundreds of open items without losing track
  • Professional persistence — comfortable following up repeatedly with suppliers and customers who don't respond
  • Clear written communication for correspondence with domestic and international suppliers and with customer quality teams
Preferred qualifications
  • Bilingual English/Spanish, written and verbal
  • HACCP and/or PCQI certification
  • Direct experience with SQF Edition 9, FSVP, or supplier approval programs
  • Experience with customer compliance portals such as ReposiTrak, TraceGains, or FoodLogiQ
  • Background in spices, botanicals, dried produce, or other high-risk imported ingredients
  • Experience preparing for or participating in third-party audits or FDA inspections
Location: Pico Rivera, CA (on-site)
Reports to: Quality Assurance Manager
Scope: Supports both De Silva Brothers amp; Company and GP De Silva Spices, Inc.
Status: Full-time, non-exempt (hourly, overtime eligible)
Pay scale: $31.00 – $37.00 per hour
About the role
We run two food businesses out of one campus. De Silva Brothers amp; Company is an SQF-certified blending and co-packing operation. GP De Silva Spices is a wholesale importer and distributor of dried chiles, spices, herbs, grains and seeds, and serves as FSVP importer of record for product sourced from Mexico, Peru, India, China and Nigeria.
Both run on documentation. Supplier files, customer specifications, controlled SOPs, training records, lab results, audit packets — if the paper isn't right, the product doesn't ship and the audit doesn't pass.
This role owns that paper. You will be the person who knows, at any moment, which supplier certificates are current, which customer portals need updating, which SOPs are due for review, and which lab results are still outstanding. When an auditor, a customer, or the FDA asks for a record, you produce it the same day.
This is a systems and records role, not a floor QA role. Product disposition, CCP decisions, and supplier approval authority rest with the QA Manager. You build and defend the documentation those decisions stand on.
What you'll ownSupplier documentation and approval records
  • Request, collect, review for completeness, and file all required supplier documents for both entities
  • Track expiration dates and drive renewals on a standing cadence (60- and 30-day notice), escalating non-responsive suppliers to QA and Purchasing
  • Maintain the Approved Supplier List for both entities and keep it reconciled with purchasing records
  • Manage the full document set: supplier questionnaires, GFSI certificates (SQF, BRCGS, FSSC 22000) and audit reports, continuing guaranties and letters of guarantee, allergen and sesame declarations, specifications, COAs (micro, heavy metals, mycotoxin, pesticide), country-of-origin and traceability records, Prop 65 statements, kosher and organic certifications, FDA registration numbers, insurance certificates and W-9s
  • Verify that incoming lots arrive with required documentation before release; flag gaps to QA and Receiving
  • Maintain FSVP supporting records under the direction of the QA Manager
Customer and co-pack documentation
  • Complete customer specification forms, quality questionnaires, and vendor qualification packets
  • Maintain company profiles and document uploads in customer compliance portals (ReposiTrak, TraceGains, FoodLogiQ and similar)
  • Issue company letters of guarantee, allergen statements, Prop 65 statements, and claim documentation to customers
  • Serve as the first point of contact for routine customer documentation requests
Internal document control
  • Administer the controlled document system: version control, issuance, revision history, and retrieval of obsolete copies
  • Maintain the annual SOP and policy review calendar and prompt document owners ahead of due dates
  • Administer training records — GMP, food safety, allergen, and new-hire onboarding — and track refresher due dates
Lab and testing coordination
  • Schedule third-party lab submissions and maintain sample chain-of-custody records
  • Track results against specification and escalate out-of-spec findings immediately to the QA Manager
  • Maintain the testing calendar and environmental monitoring records
Audit, certification, and program administration
  • Prepare documentation packets and coordinate logistics for SQF audits, customer audits, kosher inspections, and FDA inspections
  • Schedule internal audits and track findings and corrective actions to closure
  • Administer mock recall and traceability exercises and compile the results
  • Maintain the CAPA log, supplier nonconformance log, and customer complaint log
  • Manage kosher ingredient submissions and annual certification renewals
Regulatory monitoring
  • Monitor FDA import alerts, refusal reports, and recall notices against the active supplier list and current inventory; escalate hits to QA and Purchasing
What success looks like
  • 90 days: You know both supplier lists cold, have audited every file, and delivered a gap report showing what's missing or expired.
  • 6 months: No expired documents on active suppliers. Renewals go out on schedule without prompting. Customer documentation requests are answered same-day.
  • 12 months: Documentation is a non-issue in the SQF audit. Any record — supplier, customer, training, or lab — can be produced on request within the hour.
Required qualifications
  • 2–4 years in food industry quality assurance, document control, regulatory compliance, or supplier management
  • Working familiarity with HACCP, GMPs, and FSMA, and the ability to learn SQF and FSVP recordkeeping requirements quickly
  • Strong Excel skills (filtering, lookups, tracking logs) and comfort with document management systems and web-based customer portals
  • Exceptional attention to detail and follow-through; able to manage hundreds of open items without losing track
  • Professional persistence — comfortable following up repeatedly with suppliers and customers who don't respond
  • Clear written communication for correspondence with domestic and international suppliers and with customer quality teams
Benefits
  • Medical, Dental, Vision amp; Life Insurance
  • 401 (k)
  • 401 (k) Match
  • Vacation, Sick, and Holiday Pay

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