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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

$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 ...

Aerotek

Medical Device Assembler

Lake Forest, CA · On-site

$19.25 - $23.50/hr

... device assembly and packaging for medical device products. This role requires strong manual ... Monitor your own work to ensure accuracy, thoroughness, and consistent quality, promptly ...

DenMat Holdings, LLC

QC Technician

Lompoc, CA · On-site

$19.50 - $25/hr

Education and/or Experience High school diploma or general education degree (GED) and one year of experience in medical device quality control. Associates degree (AS) in life sciences from two-year ...

Intellectt INC

Quality Control Technician/ QC

Pomona, CA · On-site

$20 - $25/hr

We are seeking a detail-oriented Quality Control Technician to support the Quality Management System in a medical device manufacturing environment. The ideal candidate will perform product testing ...

Intellectt INC

QA / QC Inspector

Milpitas, CA · On-site

Role: QC Inspector Location: Milpitas, CA - 950335 Duration: 03 Months Schedule: 8:30 AM - 5:30 PM ... Experience in medical device, diagnostic, or pharma-regulated industries. Good Manufacturing ...

Intellectt INC

Quality Control Technician

Pomona, CA · On-site

$18.75 - $24/hr

Pomona, CA Duration: 6 months Shift: 8:00 AM - 5:00 PM Job Summary We are seeking a Quality Control Technician to support the Quality Management System in a medical device manufacturing environment.

Heartflow

Staff Device Quality Engineer

San Francisco, CA · On-site

$84K - $109K/yr

... medical device regulations, ensuring that our digital health solutions-including Software as a ... control process within Heartflow's Software Development Lifecycle (SDLC). You will ensure that ...

Marquee Staffing - OC

Be Seen First

Medical Device Assembler, Weekend Day 3/12 Schedule

Irvine, CA · On-site

$19 - $20/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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Medical Device Quality Control information

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

As of Aug 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 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 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.

Is medical device quality control a good career?

Medical device quality control involves inspecting and testing devices to ensure they meet safety and regulatory standards, often requiring knowledge of quality management systems and industry regulations. It offers stable employment opportunities with potential for advancement and typically requires attention to detail and relevant certifications. The field is essential for patient safety and is considered a reliable career path within the healthcare manufacturing industry.

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 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:
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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, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $44,083 per year, or $21.2 per hour.

Medical Device Quality Engineer

Prophecy Technologies

Santa Clara, CA • On-site

$84K - $109K/yr

Full-time

Posted 21 days ago

Job description

Role Overview:
This role focuses on ensuring quality and compliance within the medical device industry, specifically for a surgical robotics platform. The engineer will be responsible for design transfer, production support, and maintaining the Quality Management System (QMS) in adherence to regulatory standards.
Key Responsibilities:
  • Lead design transfer and production support activities, ensuring compliance with FDA/ISO 13485 and alignment with manufacturing readiness.
  • Own multiple subassemblies for a surgical robotics platform, ensuring design integrity, quality, and manufacturability.
  • Investigate non-conformances (NCs) using root cause analysis and drive CAPA within the QMS framework.
  • Develop and maintain FMEAs, support risk mitigation, and lead manufacturing issue resolution and qualifications (IQ/OQ/PQ).
  • Identify and implement compliant, alternative solutions to engineering and production challenges while driving continuous improvement.
  • Support and maintain Quality Management System (QMS) processes in compliance with regulatory requirements.
  • Collaborate with cross-functional teams to deliver quality-compliant outcomes.
  • Interpret and apply medical device regulations and standards to projects and processes.
  • Support audits and regulatory inspections, ensuring timely closure of actions.

Required Skills:
  • Strong understanding of Medical Device Quality Systems and regulatory compliance requirements.
  • Working knowledge of ISO 13485:2016/2019 and 21 CFR Part 820 (FDA Quality System Regulation).
  • Strong expertise in design transfer activities, including DHF ? DMR transition and compliance with FDA 21 CFR 820 & ISO 13485.
  • Sound knowledge of Medical Device Regulations, including MDD and MDR.
  • Proven experience in Non-Conformance (NC) management, CAPA processes, and internal/external audits.
  • Expertise in Medical Device Risk Management, with the ability to identify both apparent and less-obvious risks.
  • Practical experience with Application, Process, Design, and System FMEA methodologies.
  • Proficient in statistical tools and techniques, including Design of Experiments (DOE).
  • Capable of performing advanced descriptive and non-parametric statistical analyses.
  • Experienced in leveraging advanced statistical methods for reliability prediction and data-driven decision making.
  • EIS: Medical Device & Regulations

Qualifications:
  • 8+ years of experience in Medical Device Quality & Compliance.
  • Strong knowledge of ISO 13485, 21 CFR 820, MDD/MDR.
  • Expertise in Design Transfer Activities.
  • Hands-on experience in QMS, NC, CAPA, and Audits.
  • Strong expertise in Risk Management (ISO 14971), including FMEA and data-driven quality decisions.

Preferred Skills:
  • EIS: MDD Risk Management

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