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Medical Device Quality Control Jobs in California

Cordis

QC Technician - Medical Device

Irvine, CA · On-site

$20.63 - $25.65/hr

... device combination products for the treatment of coronary and peripheral artery disease. Our ... medical needs. Responsibilities The Quality Control Technician I is responsible for reviewing ...

Cordis

QC Technician - Medical Device

Irvine, CA · On-site

$20.63 - $25.65/hr

... device combination products for the treatment of coronary and peripheral artery disease. Our ... medical needs. Responsibilities The Quality Control Technician I is responsible for reviewing ...

Heartflow

Senior Device Quality Engineer

San Francisco, CA · Hybrid

$160K - $180K/yr

You will bridge the gap between rapid Agile development and rigorous medical device regulations ... Your core responsibility will be the hands-on management of the end-to-end design control process ...

Applied Medical

Quality Inspector

Lake Forest, CA · On-site

$18 - $23/hr

The Quality Inspector supports quality control activities, contributes to continuous improvement efforts, and helps maintain Applied Medical's rigorous expectations for medical device manufacturing ...

Marquee Staffing - OC

Be Seen First

Medical Device Assembler, Weekend Overnight 3/12 Schedule

Irvine, CA · On-site

$19 - $21/hr

Medical Device implant manufacturer in Irvine is seeking applicants with manufacturing experience ... Demonstrate accuracy, thoroughness and monitors own work to ensure quality. * Practice and always ...

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All JobsMedical Device Quality Control JobsMedical Device Quality Control Jobs in California

Medical Device Quality Control information

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$11

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$32

How much do medical device quality control jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for medical device quality control in California is $21.19, according to ZipRecruiter salary data. Most workers in this role earn between $17.07 and $23.70 per hour, depending on experience, location, and employer.

What is medical device quality control?

Medical Device Quality Control refers to the processes and procedures used to ensure that medical devices meet safety, quality, and regulatory standards before they reach the market. This involves rigorous inspection, testing, and documentation throughout the manufacturing process to prevent defects and ensure consistent product performance. Quality control professionals work to identify issues, monitor compliance with industry regulations like ISO 13485 and FDA requirements, and help maintain the integrity of healthcare products. Their role is crucial in protecting patient safety and upholding the reputation of medical device manufacturers.

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

To thrive in Medical Device Quality Control, you need a solid understanding of quality assurance principles, regulatory standards (such as ISO 13485 or FDA 21 CFR Part 820), and experience with inspection techniques, often supported by a degree in engineering or life sciences. Familiarity with tools like statistical process control (SPC) software, electronic quality management systems (eQMS), and documentation protocols is typical. Attention to detail, problem-solving abilities, and strong communication skills are essential soft skills for excelling in this role. These competencies are crucial for ensuring product safety, regulatory compliance, and maintaining the reputation of the medical device manufacturer.

What are some common challenges faced in a medical device quality control role, and how can I prepare for them?

Professionals in Medical Device Quality Control often face challenges such as keeping up with evolving regulatory standards, managing documentation for audits, and ensuring consistent product quality across batches. To prepare, it's helpful to develop strong attention to detail, stay updated on FDA and ISO guidelines, and build effective communication skills to collaborate with cross-functional teams like manufacturing and R&D. Being proactive in identifying potential risks and participating in continuous improvement initiatives can also help you succeed in this role.

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

AspectMedical Device Quality ControlMedical Device Quality Assurance
FocusInspecting and testing products to identify defectsDeveloping and maintaining quality systems and processes
ActivitiesProduct testing, inspection, samplingAudits, process validation, compliance management
CertificationsISO 13485, GMP trainingISO 13485, regulatory standards
Work EnvironmentLaboratories, manufacturing floorsQuality departments, regulatory offices

Medical Device Quality Control focuses on testing and inspecting products to ensure they meet quality standards, while Medical Device Quality Assurance emphasizes establishing systems and processes to prevent defects and ensure compliance. Both roles are essential in maintaining high-quality medical devices and often work closely within the industry.

What are popular job titles related to Medical Device Quality Control jobs in California?

For Medical Device Quality Control jobs in California, the most frequently searched job titles are:

What job categories do people searching Medical Device Quality Control jobs in California look for?

The top searched job categories for Medical Device Quality Control jobs in California are:

What cities in California are hiring for Medical Device Quality Control jobs?

Cities in California with the most Medical Device Quality Control job openings:

Medical Device Quality Control jobs near you
Infographic showing various Medical Device Quality Control job openings in California as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 12% Part Time, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $44,083 per year, or $21.2 per hour.

Quality Control Inspector

Industrial - Quest Staffing Services

Camarillo, CA • On-site

Full-time

Posted 17 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