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Fda Inspector Jobs in Long Beach, CA (NOW HIRING)

Prismatik

Document Control Specialist

Irvine, CA · On-site +1

$23 - $25/hr

Assists in Food and Drug Administration (FDA) inspections and Notified Body audits regarding marketed products, as requested. * Tracks and facilitates timely documentation review and implementation.

W3Global Inc.

Assistant Project Coordinator

Ontario, CA · On-site

$31 - $35/hr

This position requires a proactive professional with strong knowledge of FDA regulations, GMP, supplier quality management, inspections, auditing, and continuous improvement. Key Responsibilities 1. ...

Prescott's, Inc

Quality Assurance Specialist

Costa Mesa, CA · On-site

$65K - $70K/yr

... FDA QSR (21 CFR Part 820), and other applicable regulatory requirements. * Create, revise, and maintain quality documentation, including work instructions, inspection checklists, SOPs, and inspection ...

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All JobsFda Inspector JobsFda Inspector Jobs in Long Beach, CA

Fda Inspector information

See Long Beach, CA salary details

$25.8K

$57.8K

$104.1K

How much do fda inspector jobs pay per year?

As of Aug 15, 2026, the average yearly pay for fda inspector in Long Beach, CA is $57,767.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,500.00 and $66,800.00 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 job categories do people searching Fda Inspector jobs in Long Beach, CA look for?

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

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

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

Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in Long Beach, CA as of August 2026, with employment types broken down into 79% Full Time, 9% Part Time, 11% Contract, and 1% Nights. Highlights an 97% Physical, and 3% Remote job distribution, with an average salary of $57,767 per year, or $27.8 per hour.

Senior Manager, Quality Engineering

BiVACOR Inc

Huntington Beach, CA • On-site

$155 - $169.99/hr

Other

Re-posted 18 days ago

Job description

Help Us Build the Future of the Human Heart.

At BiVACOR, we’re developing the world’s most advanced total artificial heart, a technology capable of saving millions of lives around the world. We’re a team united by purpose, working on something truly unprecedented. Every process you validate, every fixture you design, and every challenge you overcome plays a direct role in giving patients a second chance at life. If that’s the kind of work that gets you out of bed in the morning, we’d love to meet you.

About the Role

This is a high-impact leadership role at the intersection of quality engineering strategy and clinical-stage medical device development. As Senior Manager, Quality Engineering, you will serve as a principal leader within the BiVACOR quality organization, responsible for architecting and directing quality engineering functions across the full product lifecycle of the Total Artificial Heart (TAH) system, one of the most technically advanced implantable devices in development today.

This elevated role demands a visionary, technically authoritative, and operationally excellent leader with deep expertise in electrical engineering and a distinguished track record with Class III Active Implantable Medical Devices (AIMD). You will not only lead the QE team in verification and validation, manufacturing process quality, supplier controls, and regulatory compliance — you will define the strategic direction of quality engineering programs, drive enterprise-level QMS maturity, and serve as a senior executive liaison across quality, engineering, manufacturing, regulatory affairs, and clinical functions.

You will mentor and grow quality engineering talent, shape organizational quality culture, and partner with senior leadership to advance BiVACOR’s mission of bringing a life‑saving total artificial heart to patients.

Key Responsibilities Quality System Leadership & Strategy
  • Define and execute the strategic vision for the QMS, aligned with ISO 13485, 21 CFR Part 820, 803, and 806
  • Serve as the senior quality engineering authority for BSI surveillance audits and FDA inspections
  • Lead and develop a high‑performing quality engineering team, providing strategic direction and career development
  • Establish enterprise‑wide quality KPIs and present strategic recommendations to executive leadership
Verification, Validation & Design Assurance
  • Direct V&V planning, execution, and documentation for electrical, software, and system‑level protocols supporting IDE and PMA submissions
  • Approve test protocols and reports, ensuring traceability to design inputs and applicable standards (ISO 14708, IEC 60601, ISO 14971)
  • Oversee test method validation (TMV) and equipment qualification (IQ/OQ/PQ) programs
Manufacturing Quality & Nonconformance
  • Architect and enforce IPC‑A‑610 workmanship standards for electronic assemblies across the TAH system
  • Own the nonconformance (NC) and QCIR programs, including MRB disposition, root cause investigation, and CAPA linkage
  • Drive systemic resolution of manufacturing quality escapes with root cause rigor
Risk Management & CAPA
  • Lead FMEA, FTA, and risk management file strategy at the program level per ISO 14971
  • Own and govern the enterprise CAPA process from initiation through effectiveness verification
  • Evaluate field performance data and clinical feedback to identify and mitigate systemic quality risks
Supplier Quality
  • Architect and lead the end‑to‑end supplier quality program: qualification, performance monitoring, audits, and corrective actions
  • Conduct strategic on‑site audits with focus on high‑risk and sole‑source AIMD‑critical suppliers
  • Partner with engineering and procurement to assess supply chain risk and maintain the approved supplier list (ASL)
Cross‑Functional & Regulatory Leadership
  • Serve as the senior quality engineering representative in executive program reviews and manufacturing readiness assessments
  • Lead quality engineering strategy for IDE supplements, PMA modules, and FDA information requests
  • Influence and align R&D, Regulatory Affairs, Software, and Manufacturing Engineering on quality strategy throughout the product lifecycle
Continuous Improvement
  • Define and lead the organizational continuous improvement strategy using Lean, Six Sigma, or equivalent methodologies
  • Sponsor initiatives to reduce defect rates, improve first‑pass yield, and optimize QMS processes
  • Present improvement initiative outcomes and strategic impact to executive leadership
What You Bring
  • Bachelor’s degree or higher in Electrical Engineering (mandatory)
  • Minimum 18 years of experience in the medical device industry, including demonstrated senior quality engineering leadership
  • Direct experience with Class III Active Implantable Medical Devices (AIMD), including deep knowledge of FDA IDE/PMA regulatory requirements
  • IPC‑A‑610 and/or IPC‑A‑620 certification strongly preferred
Technical Expertise
  • Expert knowledge of IEC 60601 series, ISO 14971, ISO 13485, and 21 CFR Part 820, 803, and 806
  • Deep experience with electrical and electromechanical system qualification for implantable devices
  • Proficiency in FMEA, FTA, statistical analysis, MSA/Gage R&R, and reliability methodology
  • Experience with EO sterilization qualification, cleanroom operations, and QMS software platforms
Leadership & Influence
  • Proven track record of building and inspiring senior quality engineering teams
  • Demonstrated ability to influence executive stakeholders and drive enterprise‑level quality strategy
  • Experience representing quality at a senior level in FDA or notified body inspections
  • Track record of leading cross‑functional V&V programs for complex regulatory submissions
Highly Desirable
  • VAD or Total Artificial Heart experience
  • ASQ certification (CQE, CQM/OE, or CRE)
  • Familiarity with Enlil, Arena, or comparable QMS/PLM platforms
  • Experience with IDE clinical studies and associated quality system requirements

The expected salary range for this position based in Huntington Beach California is $155,000 - $169,990. Actual pay will be determined based on experience, qualifications, geographic location, and other job‑related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Relocation benefits are not available for this posting.

Apply today and be part of something extraordinary.

BiVACOR is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

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