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Medical Device Quality Control Inspector Jobs in California

Quest Staffing Services, Inc.

Be Seen First

Quality Control Inspector

Camarillo, CA · On-site

$49K/yr

Immediate Opening! Quality Control Inspector We are seeking a highly detail-oriented Quality ... medical device regulations, meticulous documentation habits, and a collaborative approach to ...

Virco Talent

QC Inspector

Santa Fe Springs, CA · On-site

QC Inspector We are seeking a Quality Control (QC) Inspector to join our team in Santa Fe Springs ... Minimum of 2 years of QC experience, with at least 1 year of experience in the Medical Device ...

Virco Talent

QC Inspector

Santa Fe Springs, CA · On-site

QC Inspector We are seeking a Quality Control (QC) Inspector to join our team in Santa Fe Springs ... Minimum of 2 years of QC experience, with at least 1 year of experience in the Medical Device ...

KORE1 Technologies

Quality Control Inspector

Irvine, CA · On-site

$26 - $28/hr

The QC Inspector examines items for defects in materials, work, and damage. The Inspector is ... A minimum of 1-3 years' experience working in a regulated environment, medical device or pharma ...

BioPhase Solutions

QC Inspector

San Diego, CA · On-site

$18 - $19.80/hr

Quality Control Inspector Are you passionate about ensuring the highest quality standards in the ... Experience in a medical device high-volume manufacturing environment is strongly desired. * Ability ...

Lancesoft INC

QC Inspector

Camarillo, CA · On-site

$22 - $24/hr

Quality Control Inspector Full Time | Location: Camarillo, CA 93011 Reports To: Quality Control ... pharmaceutical or medical device environment. * Solid organizational and planning skills.

Crossroads Staffing Services, Inc.

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Quality Control Inspector

Camarillo, CA · On-site

$24 - $32/hr

... performs various quality control inspections, checks, and tests of products during the ... Experience in a manufacturing, pharmaceutical or medical device environment * Documentation skills ...

OrthAlign

Senior Quality Control Inspector

Irvine, CA · On-site

$30/hr

OrthAlign, Inc., a Smart Technologies, growing medical device company, has an immediate opening for a Senior Quality Control Inspector. This role supports all quality initiatives and is responsible ...

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Medical Device Quality Control Inspector information

What does a medical device quality control inspector do?

A Medical Device Quality Control Inspector is responsible for examining medical devices during and after production to ensure they meet all regulatory, quality, and safety standards. This involves inspecting products for defects, verifying measurements, and ensuring compliance with industry regulations such as FDA and ISO standards. Inspectors document their findings, report any issues, and may recommend corrective actions to improve quality. Their work is critical to ensuring that only safe and effective medical devices reach healthcare providers and patients.

What are the key skills and qualifications needed to thrive as a medical device quality control inspector?

To excel as a Medical Device Quality Control Inspector, you need a solid understanding of quality assurance principles, regulatory standards (such as ISO 13485 or FDA requirements), and a background in science or engineering. Familiarity with inspection tools like calipers, micrometers, and statistical process control software is typically required, along with any relevant quality certifications (e.g., ASQ CQI). Attention to detail, analytical thinking, and effective communication are crucial soft skills for identifying defects and collaborating with production teams. These competencies ensure product safety, regulatory compliance, and the consistent delivery of high-quality medical devices.

What are some common challenges faced by medical device quality control inspectors, and how can they be addressed?

Medical Device Quality Control Inspectors often face challenges such as keeping up with evolving regulatory standards, ensuring precise documentation, and maintaining consistency during inspections of complex products. To address these, inspectors should stay updated through regular training, closely follow Standard Operating Procedures (SOPs), and use checklists to ensure thoroughness. Collaboration with engineering, production, and regulatory teams is also essential to resolve issues promptly and ensure compliance with industry regulations.

What is the difference between Medical Device Quality Control Inspector vs Quality Assurance Technician?

AspectMedical Device Quality Control InspectorQuality Assurance Technician
CertificationsISO 13485, FDA regulationsISO 9001, GMP training
Work EnvironmentManufacturing, lab settingsProduction lines, labs
Employer & IndustryMedical device manufacturingVarious manufacturing sectors

The Medical Device Quality Control Inspector focuses on inspecting and testing medical devices to ensure compliance with industry standards, while the Quality Assurance Technician oversees broader quality processes, including documentation and process improvements. Both roles require similar certifications and often work in manufacturing environments, but their primary responsibilities differ in scope and focus.

Infographic showing various Medical Device Quality Control Inspector job openings in California as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, 2% Temporary, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Quality Control Inspector

Camarillo, CA

Industrial - Quest Staffing Services
See more jobs at Industrial - Quest Staffing Servicesexternal

Full-time

Posted 21 days ago

Job description

Immediate Opening! Quality Control Inspector
We are seeking a highly detail-oriented Quality Control Inspector to test and inspect materials, parts, and products at various stages of production. This role is ideal for a dedicated quality professional with a strong background in pharmaceutical or medical device regulations, meticulous documentation habits, and a collaborative approach to continuous improvement.
Key Responsibilities
  • Perform incoming, first article, in-process, and final inspections to ensure full compliance with company and regulatory standards
  • Initiate nonconformance reports (NCR) for any non-conforming materials identified during operations
  • Review, complete, and release manufacturing job order documents using Good Documentation Practices (GDP)
  • Approve or reject raw materials based on established quality standards and communicate findings to all required parties
  • Support cross-functional investigations into non-conformance findings and provide recommendations for process improvements
  • Perform critical pre- and post-inspection steps for products undergoing the gamma irradiation process
  • Compile quality metrics data and regularly submit structured reports to the QC Supervisor or Lead
  • Maintain a safe, orderly workspace and wear full personal protective equipment (PPE) including scrubs, coveralls, masks, and eyewear in an ISO cleanroom environment
Qualifications
  • High School Diploma or equivalent required
  • Minimum 3 years of experience in manufacturing quality control inspections
  • At least 1 year of experience handling technical documentation and corrective actions in a pharmaceutical or medical device setting
  • Working knowledge of global regulations, including ISO 9001, ISO 13485, and 21 CFR Parts 210, 211, or 820
  • Proven ability to execute strict GMP operations by following detailed Standard Operating Procedures (SOPs)
  • Hands-on experience using precision measuring devices such as calipers, rulers, tape measures, and pin gauges
  • Solid basic mathematics, computer proficiency, and preferred working knowledge of ERP systems (such as SyteLine)
  • Strong interpersonal and communication skills to effectively collaborate across internal departments and external vendors
Why Join Us?
  • Critical quality ownership role within a highly regulated, precision-driven manufacturing facility
  • Opportunity to participate directly in continuous improvement initiatives and cross-functional team investigations
  • Structured and safe work environment with an uncompromising commitment to compliance and product integrity
  • Stable position offering professional growth in advanced pharmaceutical and medical device quality standards