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Fda Inspector Jobs in California (NOW HIRING)

Stryker

Sr. Manufacturing Engineer

Ventura, CA · On-site

$85K - $142K/yr

Ensure manufacturing documentation (DHR, DMR, batch records) is complete, accurate, and inspection-ready * Support internal, customer, and regulatory audits (FDA, Notified Body); prepare responses to ...

Stryker

Sr. Manufacturing Engineer

Ventura, CA · On-site

$85K - $142K/yr

Ensure manufacturing documentation (DHR, DMR, batch records) is complete, accurate, and inspection-ready * Support internal, customer, and regulatory audits (FDA, Notified Body); prepare responses to ...

Puretek Corporation

QA Inspector

San Fernando, CA · On-site

$22 - $23/hr

Knowledge of drug cGMPs, SOPs, and regulatory guidelines including FDA requirements. * Knowledge of ... Reasoning Ability The QA Line Inspector must be able to analyze and interpret data relating to ...

Puretek Corporation

QA Inspector

San Fernando, CA · On-site

$22 - $23/hr

Knowledge of drug cGMPs, SOPs, and regulatory guidelines including FDA requirements. * Knowledge of ... Reasoning Ability The QA Line Inspector must be able to analyze and interpret data relating to ...

NCSL International

QC DIRECTOR

Rocklin, CA · On-site

$180 - $240/hr

Maintain permanent FDA inspection readiness, coordinate all QC audit documentation, on‑site walkthrough and observation remediation tracking. * Establish and continuously update full suite of lab ...

Califesciences

QC DIRECTOR

Santa Rosa, CA · On-site

$180 - $240/hr

Maintain permanent FDA inspection readiness, coordinate all QC audit documentation, on‑site walkthrough and observation remediation tracking; * Establish and continuously update full suite of lab ...

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All JobsFda Inspector JobsFda Inspector Jobs in California

Fda Inspector information

See California salary details

$24.2K

$54.2K

$97.7K

How much do fda inspector jobs pay per year?

As of Aug 13, 2026, the average yearly pay for fda inspector in California is $54,220.00, according to ZipRecruiter salary data. Most workers in this role earn between $38,000.00 and $62,700.00 per year, depending on experience, location, and employer.

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.

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.

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 the FDA's specialized training program and often require a background check and security clearance; some positions may also require state licensure or certifications. Strong attention to detail, knowledge of regulatory standards, and good communication skills are essential for the role.

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 the most commonly searched types of Fda Inspector jobs in California?

The most popular types of Fda Inspector jobs in California are:

What are popular job titles related to Fda Inspector jobs in California?

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

What job categories do people searching Fda Inspector jobs in California look for?

The top searched job categories for Fda Inspector jobs in California are:

What cities in California are hiring for Fda Inspector jobs?

Cities in California with the most Fda Inspector job openings:

Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in California as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $54,220 per year, or $26.1 per hour.

Principal Supplier Quality Engineer

THINK Surgical, Inc.

Fremont, CA • On-site

$165K - $180K/yr

Full-time

Re-posted 7 days ago

Job description

JOB SUMMARY

The Principal Supplier Quality Engineer is the company’s technical leader and subject matter expert for supplier quality management. This position is responsible for developing, implementing, and continuously improving supplier quality systems and supplier performance programs to ensure the consistent delivery of conforming products and services throughout the supply chain.

The Principal Supplier Quality Engineer leads complex supplier quality initiatives, drives supplier quality strategy, mentors quality professionals, and provides leadership in resolving high-risk supplier quality issues. This position plays a critical role in ensuring product quality, patient safety, supply continuity, and regulatory compliance. This position is based in the Fremont, CA office.

DUTIES & RESPONSIBILITIES

  • Lead the development, implementation, and continuous improvement of the company's Supplier Quality Management Program, including supplier management, supplier controls, supplier auditing, supplier monitoring, supplier risk management, and supplier performance processes.
  • Evaluate existing supplier quality systems and implement improvements to harmonize supplier quality practices with FDA QMSR, ISO 13485, ISO 14971, and industry best practices.
  • Manage supplier quality activities throughout the supplier lifecycle, including supplier qualification, monitoring, re-evaluation, development, and disqualification.
  • Lead qualification and oversight of contract manufacturers, sterilization providers, critical suppliers, and other external providers.
  • Plan, conduct, and report supplier audits and supplier assessments to evaluate compliance with quality system, regulatory, and contractual requirements.
  • Establish and maintain supplier quality metrics, supplier scorecards, supplier risk profiles, and supplier performance monitoring programs.
  • Investigate supplier-related quality issues and drive timely resolution through effective root cause analysis, corrective actions, and supplier engagement.
  • Initiate, manage, and close Supplier Corrective Action Requests (SCARs) and monitor supplier effectiveness activities.
  • Evaluate supplier nonconformances and determine appropriate containment, disposition, escalation, and risk mitigation activities.
  • Support incoming inspection activities, supplier issue resolution, supplier change notifications, and supplier process validation activities, as required.
  • Assess the impact of supplier changes on product quality, regulatory compliance, risk management documentation, and product performance.
  • Partner cross-functionally with Engineering, Operations, Manufacturing, Supply Chain, Regulatory Affairs, and externals suppliers to ensure supplier quality requirements are effectively defined, implemented, maintained, and in compliance with FDA Quality Management System Regulation (21 CFR Part 820/QMSR), ISO 13485, ISO 14971, and other applicable regulatory requirements.
  • Support new product development, sustaining engineering, supplier transfer, and supplier qualification activities.
  • Develop and maintain supplier quality procedures, work instructions, forms, templates, and records.
  • Support internal audits, notified body audits, customer audits, FDA inspections, and supplier-related regulatory activities.
  • Support Management Review through supplier quality performance reporting, supplier risk reporting, and quality trend analysis.
  • Provide technical leadership and subject matter expertise for supplier quality, supplier controls, supplier auditing, and supplier risk management activities.
  • Mentor team members and promote adoption of best practices in supplier quality management.
  • Apply risk-based decision making in accordance with ISO 14971 and company procedures.
  • Perform other duties as assigned.

SUPERVISORY RESPONSIBILITIES

  • N/A

QUALIFICATIONS

Required:

  • Bachelor's degree in Engineering, Science, or related discipline, or an equivalent experience.
  • Minimum 8-10 years of Quality Assurance and/or Supplier Quality experience within the medical device industry.
  • Strong working knowledge of FDA 21 CFR Part 820/QMSR, ISO 13485, ISO 14971, and supplier control requirements.
  • Demonstrated experience qualifying, monitoring, developing, and auditing suppliers.
  • Demonstrated experience managing Supplier Corrective Action Requests (SCARs).
  • Experience conducting investigations, root cause analysis, and corrective action activities.
  • Experience with manufacturing processes, process validation, supplier controls, and quality system requirements.
  • Strong analytical, organizational, and problem-solving skills.
  • Strong written and verbal communication skills.
  • Ability to independently manage multiple priorities and projects.
  • Knowledge of Good Manufacturing Practices (GMP) and applicable Quality System Standards.

Preferred:

  • ASQ Certified Quality Engineer (CQE), Certified Supplier Quality Professional (CSQP), Certified Quality Auditor (CQA), or ISO 13485 Lead Auditor certification.
  • Experience auditing contract manufacturers and critical suppliers.
  • Experience with supplier quality management within medical robotics, orthopedic implants, capital equipment, or electromechanical devices.
  • Experience supporting FDA inspections and notified body audits.
  • Experience with supplier scorecards, KPI development, and quality data analytics.
  • Experience with eQMS systems (e.g., Propel, MasterControl, Arena, etc.).

COMPETENCIES

  • Drive results
  • Decision quality
  • Supplier relationship management
  • Problem solving and root cause analysis
  • Strategic thinking
  • Technical leadership
  • Continuous improvement
  • Attention to detail
  • Risk-based thinking
  • Process improvement
  • Project leadership
  • Effective communication and collaboration
  • Business acumen

PHYSICAL DEMANDS & WORK ENVIRONMENT

  • Must be able to remain in a stationary position and operate office equipment for a prolonged period of time.
  • Physical activities include, but not limited to constant manual dexterity, moving about the work site, and/or handling objects weighing up to 20 lbs.
  • Other infrequent physical activities include, but not limited to, positioning self to complete assigned tasks, and ascending/descending floors and/or ladders.
  • Occasionally work around moving mechanical parts.
  • Must be able to work in a schedule that commensurate with business operation, including work during weekends, holidays and/or times outside of normal business hours.
  • Must be able to travel as business necessitates (up to 50%).

Disclaimer:

The above is intended to describe the general content of and requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities, or physical requirements. Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time. Reasonable accommodations may be possible to enable individuals with disabilities to perform the essential functions.

THINK Surgical, Inc. (“THINK”) is committed to hiring the best qualified candidates for approved positions while engaging in recruitment and selection practices that are in compliance with all applicable employment laws. It is the policy of THINK to provide equal employment opportunity for employment to all applicants and employees, regardless of any protected status. Any qualified applicant or employee with a disability who requires an accommodation in connection with their employment at THINK should contact Human Resources and request an accommodation. THINK also participates in E-Verify, a web-based system that allows THINK to confirm an employee’s eligibility to work in the United States. Actual compensation offered will depend on several factors including but not limited to geographic location, work experience, education, skill level, and/or other business and organizational needs.