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Fda Inspector Jobs in Seattle, WA (NOW HIRING)

SystImmune, Inc

Quality Assurance Manager

Redmond, WA · On-site

$120K - $160K/yr

Lead FDA inspection readiness and audits for bioanalytical laboratories, including preparation, hosting, and response management * Lead internal audits and inspection readiness for CLIA/CAP and ...

Systimmune

Quality Assurance Manager

Redmond, WA · On-site

$120K - $160K/yr

Lead FDA inspection readiness and audits for bioanalytical laboratories, including preparation, hosting, and response management * Lead internal audits and inspection readiness for CLIA/CAP and ...

UNAVAILABLE

QC Inspector

Bothell, WA

$41K - $66K/yr

Participates in FDA/ISO inspections and customer audits and maintain ongoing audit readiness * Perform other relevant duties as may be assigned by management * Act as Quality ambassador providing ...

Bruker

QC Inspector

Bothell, WA

$41K - $66K/yr

Participates in FDA/ISO inspections and customer audits and maintain ongoing audit readiness * Perform other relevant duties as may be assigned by management * Act as Quality ambassador providing ...

Bruker Corporation

QC Inspector

Bothell, WA · On-site

$41K - $66K/yr

Participates in FDA/ISO inspections and customer audits and maintain ongoing audit readiness * Perform other relevant duties as may be assigned by management * Act as Quality ambassador providing ...

Bruker Corporation

QC Inspector

Bothell, WA

$41K - $66K/yr

Participates in FDA/ISO inspections and customer audits and maintain ongoing audit readiness * Perform other relevant duties as may be assigned by management * Act as Quality ambassador providing ...

BPI Medical

Quality Control Inspector

Fife, WA · On-site

Performing visual inspections, measurements, and functional tests on medical devices to verify their compliance with applicable regulations and standards, such as ISO 13485 and FDA guidelines.

Verathon, Inc.

Quality Inspector III

Bothell, WA

$24.03 - $31.75/hr

The Quality Inspector is responsible for supporting the Quality and Operations teams by performing ... FDA cGMP regulations desirable Ability to lift 40 pounds Salary range - $24.03 - $31.75 ...

BPI Medical

Quality Control Inspector

Fife, WA · On-site

Performing visual inspections, measurements, and functional tests on medical devices to verify their compliance with applicable regulations and standards, such as ISO 13485 and FDA guidelines.

Verathon Inc.

Quality Inspector III

Bothell, WA · On-site

$24.03 - $31.75/hr

Quality Inspector III Location US-WA-Bothell ID 2025-1663 Category Quality Assurance/Regulatory ... Familiarity with ISO 13485 and FDA cGMP regulations desirable * Ability to lift 40 pounds Salary ...

Verathon, Inc.

Quality Inspector III

Bothell, WA

$24.03 - $31.75/hr

The Quality Inspector is responsible for supporting the Quality and Operations teams by performing ... FDA cGMP regulations desirable • Ability to lift 40 pounds Salary range - $24.03 - $31.75 ...

Verathon, Inc.

Quality Inspector III

Bothell, WA · On-site

$24.03 - $31.75/hr

The Quality Inspector is responsible for supporting the Quality and Operations teams by performing ... FDA cGMP regulations desirable • Ability to lift 40 pounds Salary range - $24.03 - $31.75 ...

KETTLE CUISINE LLC

QA MANAGER

Everett, WA · On-site

Liaises with USDA and FDA inspectors when necessary * Trains the operational team to ensure that new process and procedures are adopted * Builds production and QA team capability to improve ...

KETTLE CUISINE LLC

QA MANAGER

Everett, WA · On-site

$100K - $120K/yr

Liaises with USDA and FDA inspectors when necessary * Trains the operational team to ensure that new process and procedures are adopted * Builds production and QA team capability to improve ...

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All JobsFda Inspector JobsFda Inspector Jobs in Seattle, WA

Fda Inspector information

See Seattle, WA salary details

$27.9K

$62.5K

$112.7K

How much do fda inspector jobs pay per year?

As of Jul 21, 2026, the average yearly pay for fda inspector in Seattle, WA is $62,521.00, according to ZipRecruiter salary data. Most workers in this role earn between $43,800.00 and $72,300.00 per year, depending on experience, location, and employer.

How much do FDA drug investigators make?

FDA drug investigators typically earn a salary ranging from $70,000 to $120,000 annually, depending on experience, location, and level of responsibility. They often hold a bachelor's degree in a relevant field and may require specialized training or certifications related to regulatory compliance and inspection procedures.

What types of facilities or products do FDA Inspectors typically 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.

What are the key skills and qualifications needed to thrive in the Fda Inspector position, and why are they important?

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 type of inspector gets paid the most?

Among FDA inspectors, senior or specialized inspectors, such as those overseeing complex manufacturing facilities or with advanced certifications, tend to earn higher salaries. Experience, certifications, and geographic location also influence pay levels for FDA inspectors. Generally, inspectors with specialized skills or leadership roles earn the most in this field.

Is it hard to get a job at FDA?

Becoming an FDA inspector can be competitive due to strict qualification requirements, including relevant experience, education, and passing civil service exams. Candidates often need a background in science, public health, or regulatory compliance, along with strong attention to detail and communication skills. The hiring process can be lengthy and involves multiple steps such as interviews and background checks.

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 manufacturing. They must pass a written exam and a background check, and often complete on-the-job training or specialized FDA training programs. Certification or licensing is not required but can enhance prospects.

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 are popular job titles related to Fda Inspector jobs in Seattle, WA? For Fda Inspector jobs in Seattle, WA, the most frequently searched job titles are:
What job categories do people searching Fda Inspector jobs in Seattle, WA look for? The top searched job categories for Fda Inspector jobs in Seattle, WA are:
What cities near Seattle, WA are hiring for Fda Inspector jobs? Cities near Seattle, WA with the most Fda Inspector job openings:
Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in Seattle, WA as of July 2026, with employment types broken down into 82% Full Time, 13% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $62,521 per year, or $30.1 per hour.
Senior CAPA FDA Lead

Senior CAPA FDA Lead

Accord Technologies Inc.

Bothell, WA • On-site

Contractor

Re-posted 4 days ago

Job description

Position : Senior CAPA FDA Lead
Location: Bothell, Washington
Visa: Any Visa
Position type: C2C

 
 
Job Description

Key Responsibilities
  • Lead FDA audit and inspection readiness activities across the business.
  • Own and present CAPA effectiveness, investigation quality, risk assessments, and HHE processes during FDA interactions.
  • Act as the primary presenter/interface for FDA inspections, regulatory meetings, and compliance discussions.
  • Review and strengthen CAPA systems to ensure regulatory compliance, effectiveness, and sustainability.
  • Drive Health Hazard Evaluation (HHE) assessments for product quality issues, complaints, deviations, recalls, and field actions.
  • Coordinate with Quality, Regulatory Affairs, Manufacturing, Engineering, Supply Chain, and Leadership teams to ensure audit preparedness.
  • Conduct gap assessments against FDA expectations and industry best practices.
  • Support mock audits, inspection simulations, and response preparation activities.
  • Ensure timely closure of audit observations, commitments, and remediation plans.
  • Mentor teams on FDA expectations, documentation standards, root cause analysis, and inspection behavior.
  • Support preparation and review of regulatory responses, including 483 responses and associated action plans where applicable.
     
Required Experience
  • 10+ years of experience in Quality, Compliance, Regulatory, or related functions within regulated industries such as Pharma, Medical Devices, Biotechnology, or Healthcare.
  • Strong hands-on experience in:
    • CAPA management systems
    • Root cause investigations
    • Health Hazard Evaluation (HHE)
    • FDA audit/inspection management
    • Regulatory compliance programs
  • Prior experience leading or presenting during FDA inspections/audits with successful outcomes.
  • Demonstrated experience handling regulatory escalations, observations, and remediation programs.
  • Strong understanding of FDA regulations, GMP, QMS, risk management, and compliance expectations.
  • Experience working in cross-functional and high-pressure audit environments.
Preferred Qualifications
  • Experience handling FDA inspections involving critical observations or remediation programs.
  • Exposure to recalls, field actions, complaint handling, and product risk evaluations.
  • Certifications in Quality or Regulatory disciplines are preferred.
  • Strong executive communication and stakeholder management skills.
     
Key Skills
  • FDA Inspection Readiness
  • CAPA Effectiveness
  • Health Hazard Evaluation (HHE)
  • Regulatory Compliance
  • Root Cause Analysis
  • Risk Assessment
  • Audit Presentation & Defense
  • Quality Systems
  • Cross-functional Leadership
  • Executive Communication
Location: Bothell, Washington
Visa: Any Visa
Position type: C2C Contract

Job Title
Senior CAPA FDA Lead
Job Description
Key Responsibilities
  • Lead FDA audit and inspection readiness activities across the business.
  • Own and present CAPA effectiveness, investigation quality, risk assessments, and HHE processes during FDA interactions.
  • Act as the primary presenter/interface for FDA inspections, regulatory meetings, and compliance discussions.
  • Review and strengthen CAPA systems to ensure regulatory compliance, effectiveness, and sustainability.
  • Drive Health Hazard Evaluation (HHE) assessments for product quality issues, complaints, deviations, recalls, and field actions.
  • Coordinate with Quality, Regulatory Affairs, Manufacturing, Engineering, Supply Chain, and Leadership teams to ensure audit preparedness.
  • Conduct gap assessments against FDA expectations and industry best practices.
  • Support mock audits, inspection simulations, and response preparation activities.
  • Ensure timely closure of audit observations, commitments, and remediation plans.
  • Mentor teams on FDA expectations, documentation standards, root cause analysis, and inspection behavior.
  • Support preparation and review of regulatory responses, including 483 responses and associated action plans where applicable.
     
Required Experience
  • 10+ years of experience in Quality, Compliance, Regulatory, or related functions within regulated industries such as Pharma, Medical Devices, Biotechnology, or Healthcare.
  • Strong hands-on experience in:
    • CAPA management systems
    • Root cause investigations
    • Health Hazard Evaluation (HHE)
    • FDA audit/inspection management
    • Regulatory compliance programs
  • Prior experience leading or presenting during FDA inspections/audits with successful outcomes.
  • Demonstrated experience handling regulatory escalations, observations, and remediation programs.
  • Strong understanding of FDA regulations, GMP, QMS, risk management, and compliance expectations.
  • Experience working in cross-functional and high-pressure audit environments.
Preferred Qualifications
  • Experience handling FDA inspections involving critical observations or remediation programs.
  • Exposure to recalls, field actions, complaint handling, and product risk evaluations.
  • Certifications in Quality or Regulatory disciplines are preferred.
  • Strong executive communication and stakeholder management skills.
     
Key Skills
  • FDA Inspection Readiness
  • CAPA Effectiveness
  • Health Hazard Evaluation (HHE)
  • Regulatory Compliance
  • Root Cause Analysis
  • Risk Assessment
  • Audit Presentation & Defense
  • Quality Systems
  • Cross-functional Leadership
  • Executive Communication